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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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Indoor insecticide-based control measures have significantly reduced transmission, yet elimination remains a distant target. Knowing the relative abundance of the primary vector species can provide transmission models with much needed information to guide targeted control measures. Moreover, understanding how existing interventions are impacting on these relative abundances highlights where alternative control (e.g., larval source management) is needed. Using the habitat suitability probabilities generated by predictive species distribution models combined with data collated from the literature, a multinomial generalized additive model was applied to produce relative abundance estimates for Anopheles arabiensis, Anopheles funestus and Anopheles gambiae\u002FAnopheles coluzzii. Using pre- and post-intervention abundance data, estimates of the effect of indoor insecticide-based interventions on these relative abundances were made and are illustrated in post-intervention maps. Conditional effect plots and relative abundance maps illustrate the individual species’ predicted habitat suitability and how they interact when in sympatry. Anopheles arabiensis and An. funestus show an affinity in habitat preference at the expense of An. gambiae\u002FAn. coluzzii, whereas increasing habitat suitability for An. gambiae\u002FAn. coluzzii is conversely less suitable for An. arabiensis but has little effect on An. funestus. Indoor insecticide-based interventions had a negative impact on the relative abundance of An. funestus, and a lesser effect on An. arabiensis. Indoor residual spraying had the greatest impact on the relative abundance of An. funestus, and a lesser effect on An. gambiae\u002FAn. coluzzii. Insecticide-treated bed nets reduced the relative abundance of both species equally. These results do not indicate changes in the absolute abundance of these species, which may be reduced for all species overall. The maps presented here highlight the interactions between the primary vector species in sub-Saharan Africa and demonstrate that An. funestus is more susceptible to certain indoor-based insecticide interventions than An. gambiae\u002FAn. coluzzii, which in turn, is more susceptible than An. arabiensis. This may provide An. arabiensis with a competitive advantage where it is found in sympatry with other more endophilic vectors, and potentially increase the need for outdoor-based vector interventions to deal with any residual transmission barring the way to malaria elimination.",{"EN":1014},"Modelling the relative abundance of the primary African vectors of malaria before and after the implementation of indoor, insecticide-based vector control",{"VOID":1016},"Coetzee M, Hunt RH, Wilkerson R, Della Torre A, Coulibaly MB, Besansky NJ. Anopheles coluzzii and Anopheles amharicus, new members of the Anopheles gambiae complex. Zootaxa. 2013;3619:246–74.\nCoetzee M. 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Am J Trop Med Hyg. 1999;61:1010–6.\nCaputo B, Nwakanma D, Jawara M, Adiamoh M, Dia I, Konate L, et al. Anopheles gambiae complex along the Gambia river, with particular reference to the molecular forms of An. gambiae s.s. Malar J. 2008;7:182.\nSchneider P, Takken W, McCall PJ. Interspecific competition between sibling species larvae of Anopheles arabiensis and An. gambiae. Med Vet Entomol. 2000;14:165–70.\nKirby MJ, Lindsay SW. Effect of temperature and inter-specific competition on the development and survival of Anopheles gambiae sensu stricto and An. arabiensis larvae. Acta Trop. 2009;109:118–23.\nPaaijmans KP, Huijben S, Githeko AK, Takken W. Competitive interactions between larvae of the malaria mosquitoes Anopheles arabiensis and Anopheles gambiae under semi-field conditions in western Kenya. Acta Trop. 2009;109:124–30.\nLyons CL, Coetzee M, Terblanche JS, Chown SL. 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Geneva: World Health Organization.\nLengeler C. Insecticide-treated bednets and curtains for preventing malaria. Cochrane Database Syst Rev. 2000;2:CD000363.\nPluess B, Tanser FC, Lengeler C, Sharp BL. Indoor residual spraying for preventing malaria. Cochrane Database Syst Rev. 2010;4:CD006657.\nBhatt S, Weiss DJ, Cameron E, Bisanzio D, Mappin B, Dalrymple U, et al. The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015. Nature. 2015;526:207–11.\nCrook SE, Baptista A. The effect of permethrin-impregnated wall-curtains on malaria transmission and morbidity in the suburbs of Maputo, Mozambique. Trop Geogr Med. 1995;47:64–7.\nGimnig JE, Vulule JM, Lo TQ, Kamau L, Kolczak MS, Phillips-Howard PA, et al. Impact of permethrin-treated bed nets on entomologic indices in an area of intense year-round malaria transmission. Am J Trop Med Hyg. 2003;68:16–22.\nKilleen GF. Characterizing, controlling and eliminating residual malaria transmission. Malar J. 2014;13:330.\nCasimiro S, Coleman M, Mohloai P, Hemingway J, Sharp B. Insecticide resistance in Anopheles funestus (Diptera: Culicidae) from Mozambique. 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a significant decrease in entomological and epidemiological indicators was reported in Cameroon since the introduction of insecticide-treated bed nets, malaria prevalence remains high also in some parts of the West Region of Cameroon. This study was designed to evaluate malaria preventive measures among patients attending the Bamendjou and Foumbot District hospitals of the West Region of Cameroon. This was a cross-sectional study carried out within a period of 3 months, from January to March 2020. Data was obtained using a structured questionnaire and laboratory analysis. The CareStart™ Pf Malaria HRP2 qualitative rapid diagnostic test was used for malaria diagnosis. The questionnaire was designed to collect information on respondent’s socio-demographic characteristics, and the use of malaria preventive measures. Data were analysed using descriptive statistics, regression analysis, and Chi-square (and Fisher’s exact) test. A total of 170 study participants were recruited in Foumbot and 197 in Bamendjou. Malaria was significantly (P \u003C 0.0001) more prevalent in Foumbot (47.06%) than in Bamendjou (19.8%). In Foumbot, non-use of insect repellent spray (P = 0.0214), insect repellent body cream (P = 0.0009), mosquito spray (P = 0.0001) and not draining stagnant water (P = 0.0004) predisposed to higher risk of malaria. In Bamendjou, non-use of insect repellent spray (P = 0.0012), long-lasting insecticidal bed nets (P = 0.0001), window and door nets (P = 0.0286), predisposed to a higher risk of malaria. Malaria prevalence was high among the study participants especially in Foumbot. An adequate follow-up to ensure effective execution of the recently launched third phase of LLINs distribution campaign in Cameroon is recommended. Additionally, integrated vector management is required to ensure effective control of malaria transmission in Foumbot and Bamendjou.",{"EN":1285},"Evaluation of malaria preventive measures among adult patients attending the Bamendjou and Foumbot district hospitals of the West Region of Cameroon",{"VOID":1287},"Doumbe-Belisse P, Ngadjeu CS, Sonhafouo-Chiana N, Talipouo A, Djamouko-Djonkam L, Kopya E, et al. High malaria transmission sustained by Anopheles gambiae s.l. occurring both indoors and outdoors in the city of Yaoundé, Cameroon. Wellcome Open Res. 2018;3:164.\nTonye SGM, Kouambeng C, Wounang R, Vounatsou P. Challenges of DHS and MIS to capture the entire pattern of malaria parasite risk and intervention effects in countries with different ecological zones: the case of Cameroon. Malar J. 2018;17:156.\nFosso AL. Une politique de santé globale dans l’arène locale. La délivrance des antipaludéens à Bandjoun au Cameroun. Anthropologie & Développement. 2015:161–95.\nBekolo CE, Williams TDA, Ngwabumba P, Ngoube S. A hang-up and behaviour change communication campaign to improve bed net use: a pilot study from the locality of Baré-Bakem in Cameroon. J Med Health Sci. 2019;20:4.\nAntonio-Nkondjio C, Ndo C, Njiokou F, Bigoga JD, Awono-Ambene P, Etang J, et al. Review of malaria situation in Cameroon: technical viewpoint on challenges and prospects for disease elimination. Parasit Vectors. 2019;12:501.\nManguin S. Anopheles mosquitoes: new insights into malaria vectors. Rijeka: IntechOpen; 2013.\nSidiki NN, Payne VK, Cedric Y, Nadia NA. Effect of impregnated mosquito bed nets on the prevalence of malaria among pregnant women in Foumban Subdivision, West Region of Cameroon. J Parasitol Res. 2020;2020:7438317.\nBowen HL. Impact of a mass media campaign on bed net use in Cameroon. Malar J. 2013;12(1):36.\nFokam EB, Dzi KT, Ngimuh L, Enyong P. The effect of long lasting insecticide bed net use on malaria prevalence in the Tombel Health District, South West Region-Cameroon. Malar Res Treat. 2016;2016:3216017.\nNdo C, Menze-Djantio B, Antonio-Nkondjio C. Awareness, attitudes and prevention of malaria in the cities of Douala and Yaoundé (Cameroon). Parasit Vectors. 2011;4:181.\nKimbi HK, Nkesa SB, Ndamukong-Nyanga JL, Sumbele IUN, Atashili J, Atanga MBS. Socio-demographic factors influencing the ownership and utilization of insecticide-treated bed nets among malaria vulnerable groups in the Buea Health District, Cameroon. BMC Res Notes. 2014;7:624.\nFokam EB, Kindzeka GF, Ngimuh L, Dzi KT, Wanji S. Determination of the predictive factors of long-lasting insecticide-treated net ownership and utilisation in the Bamenda Health District of Cameroon. BMC Public Health. 2017;17:263.\nNtonifor NH, Veyufambom S. Assessing the effective use of mosquito nets in the prevention of malaria in some parts of Mezam division, Northwest Region Cameroon. Malar J. 2016;15:390.\nGonahasa S, Maiteki-Sebuguzi C, Rugnao S, Dorsey G, Opigo J, Yeka A, et al. LLIN Evaluation in Uganda Project (LLINEUP): factors associated with ownership and use of long-lasting insecticidal nets in Uganda: a cross-sectional survey of 48 districts. Malar J. 2018;17:421.\nAntonio-Nkondjio C, Sonhafouo-Chiana N, Ngadjeu C, Doumbe-Belisse P, Talipouo A, Djamouko-Djonkam L, et al. Review of the evolution of insecticide resistance in main malaria vectors in Cameroon from 1990 to 2017. Parasit Vectors. 2017;10:472.\nEtang J, Mbida AM, Akono PN, Binyang J, Moukoko CEE, Lehman LG, et al. Anopheles coluzzii larval habitat and insecticide resistance in the island area of Manoka, Cameroon. BMC Infect Dis. 2016;16:217.\nSougoufara S, Ottih EC, Tripet F. The need for new vector control approaches targeting outdoor biting Anopheline malaria vector communities. Parasit Vectors. 2020;13:295.\nKilleen GF, Seyoum A, Sikaala C, Zomboko AS, Gimnig JE, Govella NJ, et al. Eliminating malaria vectors. Parasit Vectors. 2013;6:172.\nLazare T, Ghislain SS. Acteurs privés et approvisionnement en eau potable des populations de la commune d’Abobo (Côte d’Ivoire). Can J Trop Geogr. 2015;2:15–28.\nWHO. Global report on insecticide resistance in malaria vectors: 2010–2016. Geneva: World Health Organization; 2018.\nSamé-Ekobo A. Grands travaux et maladies à vecteurs au Cameroun: impact des aménagements ruraux et urbains sur le paludisme et autres maladies à vecteurs. IRD éditions; 2018.\nAtangana S, Foumbi J, Charlois M, Ambroise-Thomas P. Ripert C [Epidemiological study of onchocerciasis and malaria in Bamendjin dam area (Cameroon). Malacologic fauna and risks of schistosomian introduction]. Med Trop. 1979;39:537–43 (in French).\nKwenti TE, Kwenti TDB, Latz A, Njunda LA, Nkuo-Akenji T. Epidemiological and clinical profile of paediatric malaria: a cross sectional study performed on febrile children in five epidemiological strata of malaria in Cameroon. BMC Infect Dis. 2017;17:499.\nRusso G, Faggioni G, Paganotti GM, Dongho GBD, Pomponi A, De Santis R, et al. Molecular evidence of Plasmodium vivax infection in Duffy negative symptomatic individuals from Dschang West Cameroon. Malar J. 2017;16:74.\nTchuinkam T, Simard F, Lélé-Defo E, Téné-Fossog B, Tateng-Ngouateu A, Antonio-Nkondjio C, et al. Bionomics of Anopheline species and malaria transmission dynamics along an altitudinal transect in Western Cameroon. BMC Infect Dis. 2010;10:119.\nAmvongo-Adjia N, Wirsiy EL, Riveron JM, Ndongmo WPC, Enyong PA, Njiokou F, et al. Bionomics and vectorial role of anophelines in wetlands along the volcanic chain of Cameroon. Parasit Vectors. 2018;11:471.\nMfouapon A, Moupou M, Mefire J, Ngapgue J. Economical and environmental hazards of traditional packing for market garden produce used within the Foumbot agricultural region. VertigO. 2014;14:3.\nEditorial. Cameroon: Bamendjou council, others encouraged for promoting good governance. Journal du Cameroun. 2018. https:\u002F\u002Fwww.journalducameroun.com\u002F. Accessed 01 Nov 2018.\nCharan J, Biswas T. How to calculate sample size for different study designs in medical research? Indian J Psychol Med. 2013;35:121–6.\nWHO. How to use a rapid diagnostic test (RDT): a guide for training at a village and clinic level. Geneva: World Health Organization; 2009.\nDhiman SK. Malaria control: behavioural and social aspects. DRDO Sci Spectrum. 2009;183:186.\nFarogh A, Qayyum A, Haleem A, Ghaffar A. Haematological abnormalities in malaria. Biomedica. 2009;25:52–5.\nNlinwe NO, Nange TB. Assessment of hematological parameters in malaria, among adult patients attending the Bamenda Regional Hospital. Anemia. 2020;2020:3814513.\nHeggenhougen HK, Hackethal V, Vivek P. The behavioural and social aspects of malaria and its control: an introduction and annotated bibliography. Geneva: World Health Organization; 2003.\nNlinwe NO, Ateh TAE. Assessment of malaria predisposing factors among crop production farmers attending the Ndop District Hospital, Northwest Region of Cameroon. J Parasitol Res. 2020;2020:1980709.\nCarneiro I, Roca-Feltrer A, Griffin JT, Smith L, Tanner M, Schellenberg JA, et al. Age-patterns of malaria vary with severity, transmission intensity and seasonality in sub-Saharan Africa: a systematic review and pooled analysis. PLoS ONE. 2010;5:e8988.\nvan Eijk AM, Hill J, Noor AM, Snow RW, ter Kuile FO. Prevalence of malaria infection in pregnant women compared with children for tracking malaria transmission in sub-Saharan Africa: a systematic review and meta-analysis. Lancet Glob Health. 2015;3:e617–28.\nBauserman M, Conroy AL, North K, Patterson J, Bose C, Meshnick S. An overview of malaria in pregnancy. Semin Perinatol. 2019;43:282–90.\nSimon-Oke IA. Prevalence of malaria parasites among pregnant women and children under five years in Ekiti State, Southwest Nigeria. J Biomed Transl Res. 2019;5:5–10.\nEmeka PC. The impact of culture and religion on the healthcare seeking behavior amongst the residents of Anambra State, Nigeria with regards to malaria treatment. Thesis, Walden University; 2011.\nMaigemu AY, Haji HK. Influence of religion on malaria control practices among household heads in Zamfara state North West Nigeria. J Cult Soc Dev. 2015;10:78–84.\nChoonara S, Odimegwu CO, Elwange BC. Factors influencing the usage of different types of malaria prevention methods during pregnancy in Kenya. Afr Health Sci. 2015;15:413–9.\nGovere J, Durrheim D, la Grange K, Mabuza A, Booman M. Community knowledge and perceptions about malaria and practices influencing malaria control in Mpumalanga Province, South Africa. S Afr Med J. 2000;90:611–8.\nDike N, Onwujekwe O, Ojukwu J, Ikeme A, Uzochukwu B, Shu E. Influence of education and knowledge on perceptions and practices to control malaria in Southeast Nigeria. Soc Sci Med. 2006;63:103–6.\nMazigo HD, Obasy E, Mauka W, Manyiri P, Zinga M, Kweka EJ, et al. Knowledge, attitudes, and practices about malaria and its control in rural northwest Tanzania. Malar Res Treat. 2010;2010:794261.\nRehman AM, Coleman M, Schwabe C, Baltazar G, Matias A, Gomes IR, et al. How much does malaria vector control quality matter: the epidemiological impact of holed nets and inadequate indoor residual spraying. PLoS ONE. 2011;6:e19205.\nBoggild A, Brophy J, Charlebois P, Crockett M, Geduld J, Ghesquiere W, et al. Malaria: Summary of recommendations for the prevention of malaria by the Committee to Advise on Tropical Medicine and Travel (CATMAT). Can Commun Dis Rep. 2014;40:118–32.\nAsidi A, N’Guessan R, Akogbeto M, Curtis C, Rowland M. Loss of household protection from use of insecticide-treated nets against pyrethroid-resistant mosquitoes. Benin Emerg Infect Dis. 2012;18:1101.\nEdelu B, Ikefuna A, Emodi J, Adimora G. Awareness and use of insecticide-treated bed nets among children attending outpatient clinic at UNTH, Enugu-the need for an effective mobilization process. Afr Health Sci. 2010;10:117–26.\nOkumu FO, Mbeyela E, Lingamba G, Moore J, Ntamatungiro AJ, Kavishe DR, et al. Comparative field evaluation of combinations of long-lasting insecticide treated nets and indoor residual spraying, relative to either method alone, for malaria prevention in an area where the main vector is Anopheles arabiensis. Parasit Vectors. 2013;6:46.\nLindsay SW, Jawara M, Paine K, Pinder M, Walraven G, Emerson PM. Changes in house design reduce exposure to malaria mosquitoes. Trop Med Int Health. 2003;8:512–7.\nRatovonjato J, Randrianarivelojosia M, Rakotondrainibe ME, Raharimanga V, Andrianaivolambo L, Le Goff G, et al. Entomological and parasitological impacts of indoor residual spraying with DDT, alphacypermethrin and deltamethrin in the western foothill area of Madagascar. Malar J. 2014;13:21.\nGithinji EK, Irungu LW, Ndegwa PN, Machani MG, Amito RO, Kemei BJ, et al. Impact of insecticide resistance on P falciparum vectors’ biting, feeding, and resting behaviour in selected clusters in Teso North and South subcounties in Busia County, Western Kenya. J Parasitol Res. 2020;2020:9423682.\nMenze BD, Wondji MJ, Tchapga W, Tchoupo M, Riveron JM, Wondji CS. Bionomics and insecticides resistance profiling of malaria vectors at a selected site for experimental hut trials in central Cameroon. Malar J. 2018;17:317.\nNwane P, Etang J, Chouaїbou M, Toto JC, Koffi A, Mimpfoundi R, et al. Multiple insecticide resistance mechanisms in Anopheles gambiae s.l. populations from Cameroon, Central Africa. Parasit Vectors. 2013;6:41.\nAntonio-Nkondjio C, Fossog BT, Ndo C, Djantio BM, Togouet SZ, Awono-Ambene P, et al. Anopheles gambiae distribution and insecticide resistance in the cities of Douala and Yaoundé (Cameroon): influence of urban agriculture and pollution. Malar J. 2011;10:154.\nYougang AP, Kamgang B, Tedjou AN, Wilson-Bahun TA, Njiokou F, Wondji CS. Nationwide profiling of insecticide resistance in Aedes albopictus (Diptera: Culicidae) in Cameroon. PLoS ONE. 2020;15:e0234572.\nBenelli G, Beier JC. Current vector control challenges in the fight against malaria. Acta Trop. 2017;174:91–6.\nWilson AL, Chen-Hussey V, Logan JG, Lindsay SW. Are topical insect repellents effective against malaria in endemic populations? A systematic review and meta-analysis. Malar J. 2014;13:446.\nKatz TM, Miller JH, Hebert AA. Insect repellents: historical perspectives and new developments. J Am Acad Dermatol. 2008;58:865–71.\nGryseels C, Uk S, Sluydts V, Durnez L, Phoeuk P, Suon S, et al. Factors influencing the use of topical repellents: implications for the effectiveness of malaria elimination strategies. Sci Rep. 2015;5:16847.\nEtang J, Fondjo E, Chandre F, Morlais I, Brengues C, Nwane P, et al. First report of knockdown mutations in the malaria vector Anopheles gambiae from Cameroon. Am J Trop Med Hyg. 2006;74:795–7.\nGraves PM, Richards FO, Ngondi J, Emerson PM, Shargie EB, Endeshaw T, et al. Individual, household and environmental risk factors for malaria infection in Amhara, Oromia and SNNP regions of Ethiopia. Trans R Soc Trop Med Hyg. 2009;103:1211–20.\nChen-Hussey V, Carneiro I, Keomanila H, Gray R, Bannavong S, Phanalasy S, et al. Can topical insect repellents reduce malaria? A cluster-randomised controlled trial of the insect repellent N, N-diethyl-m-toluamide (DEET) in Lao PDR. PLoS ONE. 2013;8:e70664.\nRaghavendra K, Barik TK, Reddy BN, Sharma P, Dash AP. Malaria vector control: from past to future. Parasitol Res. 2011;108:757–79.\nAmoran O, Onwumbe O, Salami O, Mautin G. The influence of environmental sanitation on prevalence of malaria in a rural town in south-western Nigeria. Niger J Med. 2014;23:254–62.\nNkuo-Akenji T, Ntonifor NN, Ndukum MB, Kimbi HK, Abongwa EL, Nkwescheu A, et al. Environmental factors affecting malaria parasite prevalence in rural Bolifamba, South-West Cameroon. Afr J Health Sci. 2006;13:40–6.\nKimbi HK, Nana Y, Sumbele IN, Anchang-Kimbi JK, Lum E, Tonga C, et al. Environmental factors and preventive methods against malaria parasite prevalence in rural Bomaka and urban Molyko, Southwest Cameroon. J Bacteriol Parasitol. 2013;4:4172.\nMinakawa N, Dida GO, Sonye GO, Futami K, Njenga SM. Malaria vectors in Lake Victoria and adjacent habitats in western Kenya. PLoS ONE. 2012;7:e32725.\nAnchang-Kimbi JK, Nkweti VN, Ntonifor HN, Apinjoh TO, Tata RB, Chi HF, et al. Plasmodium falciparum parasitaemia and malaria among pregnant women at first clinic visit in the mount Cameroon Area. BMC Infect Dis. 2015;15:439.",{"VOID":1289},"10.1186\u002Fs12936-021-03592-7","https:\u002F\u002Fmalariajournal.biomedcentral.com\u002Farticles\u002F10.1186\u002Fs12936-021-03592-7",[1292,1307,1320],{"id":1293,"sortIndex":32,"researcher":28,"roles":1294,"affiliations":1295,"properties":1304,"displayName":1306,"givenName":28,"familyName":28},"e5484002-ed51-49ee-ba2e-808427e95b13",[1026],[1296],{"id":1297,"sortIndex":32,"affiliation":1298,"properties":28},"756d9320-f3af-4084-83bf-eb03e9ce9223",{"id":1297,"createTime":28,"updateTime":28,"relativeEntities":1299,"slug":28,"properties":1300,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1303,"statistic":28},[],{"title":1301},{"VI":1302}," Department of Medical Laboratory Science, The University of Bamenda, Faculty of Health Sciences, Bamenda, Cameroon",[],{"title":1305},{"VI":1306},"Nfor Omarine Nlinwe",{"id":1308,"sortIndex":40,"researcher":28,"roles":1309,"affiliations":1310,"properties":1317,"displayName":1319,"givenName":28,"familyName":28},"9144ce3a-6b3f-40c3-8c2e-a5e823968547",[1026],[1311],{"id":1297,"sortIndex":32,"affiliation":1312,"properties":28},{"id":1297,"createTime":28,"updateTime":28,"relativeEntities":1313,"slug":28,"properties":1314,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1316,"statistic":28},[],{"title":1315},{"VI":1302},[],{"title":1318},{"VI":1319},"Yengong Clinton Singong",{"id":1321,"sortIndex":123,"researcher":28,"roles":1322,"affiliations":1323,"properties":1330,"displayName":1332,"givenName":28,"familyName":28},"976c6cb4-a8f6-4673-a972-2933b2862bfe",[1026],[1324],{"id":1297,"sortIndex":32,"affiliation":1325,"properties":28},{"id":1297,"createTime":28,"updateTime":28,"relativeEntities":1326,"slug":28,"properties":1327,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1329,"statistic":28},[],{"title":1328},{"VI":1302},[],{"title":1331},{"VI":1332},"Tenkam Makamdoum Ruth Florentine",{"url":1290,"publisher":1334,"properties":1379},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1335,"slug":872,"properties":1336,"entityType":25,"verifyStatus":878,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1339,"manageAffiliations":1348,"indexDatabases":1359,"url":939,"thumbnailPath":28,"statistic":1374,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1337,"title":1338},{"VOID":875},{"EN":877},[1340,1344],{"id":881,"createTime":28,"updateTime":28,"relativeEntities":1341,"label":1342,"description":1343,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":884},{},{"id":887,"createTime":28,"updateTime":28,"relativeEntities":1345,"label":1346,"description":1347,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":890},{},[1349,1354],{"id":894,"createTime":28,"updateTime":28,"relativeEntities":1350,"slug":28,"properties":1351,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1353,"statistic":28},[],{"title":1352},{"EN":898},[],{"id":901,"createTime":28,"updateTime":28,"relativeEntities":1355,"slug":28,"properties":1356,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1358,"statistic":28},[],{"title":1357},{"EN":905},[],[1360,1367],{"id":909,"indexDatabase":1361,"url":921,"indexYears":28,"academicFieldIds":1366,"indexDatabaseRanking":28},{"id":911,"createTime":28,"updateTime":28,"relativeEntities":1362,"label":1363,"description":1364,"key":918,"publicationTags":1365,"standard":28},[],{"EN":914,"VI":914},{"EN":916,"VI":917},[920,813],[923,924,925],{"id":927,"indexDatabase":1368,"url":933,"indexYears":934,"academicFieldIds":1373,"indexDatabaseRanking":938},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":1369,"label":1370,"description":1371,"key":781,"publicationTags":1372,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[936,937],{"impactFactor":32,"impactFactorByYear":1375,"i10Index":944,"i10IndexLast5Year":945,"totalPublication":946,"totalPublicationByYear":1376,"totalCitation":963,"totalCitationByYear":1377,"totalCitationPerPublication":982,"totalCitationPerPublicationByYear":1378,"hindexLast5Year":332,"hindex":332},{"2010":513,"2012":171,"2013":366,"2014":942,"2015":120,"2016":120,"2017":226,"2018":225,"2019":225,"2020":286,"2021":943,"2022":338,"2023":229},{"2002":199,"2003":202,"2004":148,"2005":353,"2006":358,"2007":331,"2008":948,"2009":949,"2010":950,"2011":951,"2012":457,"2013":952,"2014":953,"2015":954,"2016":955,"2017":956,"2018":957,"2019":958,"2020":959,"2021":960,"2022":961,"2023":962,"2024":139},{"2005":965,"2006":966,"2007":967,"2008":968,"2009":969,"2010":970,"2011":971,"2012":972,"2013":973,"2014":974,"2015":975,"2016":976,"2017":977,"2018":978,"2019":979,"2020":980,"2021":981,"2022":155},{"2005":984,"2006":985,"2007":986,"2008":987,"2009":988,"2010":989,"2011":990,"2012":991,"2013":992,"2014":993,"2015":994,"2016":995,"2017":996,"2018":997,"2019":998,"2020":999,"2021":363,"2022":319},{"pages":1380,"volume":1381},{"VOID":1188},{"VOID":1382},"20","2021-01-22",2021,[920,938],{"id":1387,"createTime":1388,"updateTime":1389,"relativeEntities":1390,"slug":1391,"properties":1392,"entityType":1019,"verifyStatus":26,"verifyTime":1389,"verifyNote":1020,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1401,"fullTextUrl":28,"authors":1402,"publicationType":1139,"publisherRelationship":1551,"citationCount":28,"citationInfo":28,"publishDate":1602,"publishYear":975,"citationAnalyzeStatus":878,"lastCitationAnalyze":28,"indexDatabases":1603,"openAccess":28,"references":28,"isForceReanalyzing":1194},"0054f742-2d9d-4ca2-b470-cf22836817c7","2023-12-14T00:54:21.846+00:00","2025-02-25T17:42:17.189+00:00",[],"Comparison-of-molecular-tests-for-the-diagnosis-of-malaria-in-Honduras",{"abstract":1393,"title":1395,"references":1397,"doi":1399},{"EN":1394},"Honduras is a tropical country with more than 70% of its population living at risk of being infected with either Plasmodium vivax or Plasmodium falciparum. Laboratory diagnosis is a very important factor for adequate treatment and management of malaria. In Honduras, malaria is diagnosed by both, microscopy and rapid diagnostic tests and to date, no molecular methods have been implemented for routine diagnosis. However, since mixed infections, and asymptomatic and low-parasitaemic cases are difficult to detect by light microscopy alone, identifying appropriate molecular tools for diagnostic applications in Honduras deserves further study. The present study investigated the utility of different molecular tests for the diagnosis of malaria in Honduras. A total of 138 blood samples collected as part of a clinical trial to assess the efficacy of chloroquine were used: 69 microscopically confirmed P. falciparum positive samples obtained on the day of enrolment and 69 follow-up samples obtained 28 days after chloroquine treatment and shown to be malaria negative by microscopy. Sensitivity and specificity of microscopy was compared to an 18 s ribosomal RNA gene-based nested PCR, two single-PCR reactions designed to detect Plasmodium falciparum infections, one single-PCR to detect Plasmodium vivax infections, and one multiplex one-step PCR reaction to detect both parasite species. Of the 69 microscopically positive P. falciparum samples, 68 were confirmed to be P. falciparum-positive by two of the molecular tests used. The one sample not detected as P. falciparum by any of the molecular tests was shown to be P. vivax-positive by a reference molecular test indicating a misdiagnosis by microscopy. The reference molecular test detected five cases of P. vivax\u002FP. falciparum mixed infections, which were not recognized by microscopy as mixed infections. Only two of these mixed infections were recognized by a multiplex test while a P. vivax-specific polymerase chain reaction (PCR) detected three of them. In addition, one of the day 28 samples, previously determined to be malaria negative by microscopy, was shown to be P. vivax-positive by three of the molecular tests specific for this parasite. Molecular tests are valuable tools for the confirmation of Plasmodium species and in detecting mixed infections in malaria endemic regions.",{"EN":1396},"Comparison of molecular tests for the diagnosis of malaria in Honduras",{"VOID":1398},"Banjara MR, Sirawaraporn W, Petmitr S, Imwong M, Joshi AB, Chavalitshewinkoon-Petmitr P: Characteristics and risk factors of Plasmodium falciparum malaria in Eastern and Central Nepal. Kathmandu Univ Med J (KUMJ). 2009, 7: 378-382.\nPayne D: Use and limitations of light microscopy for diagnosing malaria at the primary health care level. Bull World Health Organ. 1988, 66: 621-626.\nHanscheid T, Grobusch MP: How useful is PCR in the diagnosis of malaria?. Trends Parasitol. 2002, 18: 395-398. 10.1016\u002FS1471-4922(02)02348-6.\nFuehrer HP, Fally MA, Habler VE, Starzengruber P, Swoboda P, Noedl H: Novel nested direct PCR technique for malaria diagnosis using filter paper samples. J Clin Microbiol. 2011, 49: 1628-1630. 10.1128\u002FJCM.01792-10.\nKano S, Tsuzuki K, Inaba H, Onda T, Masuda G, Suzuki M: DNA diagnosis of Plasmodium falciparum malaria by single-tube PCR. Kansenshogaku Zasshi. 1997, 71: 1090-1092.\nOsman MM, Nour BY, Sedig MF, De Bes L, Babikir AM, Mohamedani AA, Mens PF: Informed decision-making before changing to RDT: a comparison of microscopy, rapid diagnostic test and molecular techniques for the diagnosis and identification of malaria parasites in Kassala, eastern Sudan. Trop Med Int Health. 2010, 15: 1442-1448. 10.1111\u002Fj.1365-3156.2010.02659.x.\nParija SC: PCR for diagnosis of malaria. Indian J Med Res. 2010, 132: 9-10.\nRubio JM, Roche J, Berzosa PJ, Moyano E, Benito A: The potential utility of the Semi-Nested Multiplex PCR technique for the diagnosis and investigation of congenital malaria. Diagn Microbiol Infect Dis. 2000, 38: 233-236. 10.1016\u002FS0732-8893(00)00204-2.\nVo TK, Bigot P, Gazin P, Sinou V, De Pina JJ, Huynh DC, Fumoux F, Parzy D: Evaluation of a real-time PCR assay for malaria diagnosis in patients from Vietnam and in returned travellers. Trans R Soc Trop Med Hyg. 2007, 101: 422-428. 10.1016\u002Fj.trstmh.2006.09.004.\nGilks C, Pasvol G, Juel-Jensen B: Mixed malarial infection due to Plasmodium falciparum and P vivax. Br Med J (Clin Res Ed). 1985, 291: 603-604.\nMixson-Hayden T, Lucchi NW, Udhayakumar V: Evaluation of three PCR-based diagnostic assays for detecting mixed Plasmodium infection. BMC Res Notes. 2010, 3: 88-10.1186\u002F1756-0500-3-88.\nSavioli L, de Felici A, Grazia Paglia M, Visco G: Mixed malarial infection due to Plasmodium falciparum and P vivax. Br Med J (Clin Res Ed). 1985, 291: 23-24.\nEbrahimzadeh A, Fouladi B, Fazaeli A: High rate of detection of mixed infections of Plasmodium vivax and Plasmodium falciparum in South-East of Iran, using nested PCR. Parasitol Int. 2007, 56: 61-64. 10.1016\u002Fj.parint.2006.12.001.\nSnounou G, Viriyakosol S, Jarra W, Thaithong S, Brown KN: Identification of the four human malaria parasite species in field samples by the polymerase chain reaction and detection of a high prevalence of mixed infections. Mol Biochem Parasitol. 1993, 58: 283-292. 10.1016\u002F0166-6851(93)90050-8.\nDemas A, Oberstaller J, Debarry J, Lucchi NW, Srinivasamoorthy G, Sumari D, Kabanywanyi AM, Villegas L, Escalante AA, Kachur SP, Barnwell JW, Peterson DS, Udhayakumar V, Kissinger JC: Applied genomics: data mining reveals species-specific malaria diagnostic targets more sensitive than 18S rRNA. J Clin Microbiol. 2011, 49: 2411-2418. 10.1128\u002FJCM.02603-10.\nSingh B, Bobogare A, Cox-Singh J, Snounou G, Abdullah MS, Rahman HA: A genus- and species-specific nested polymerase chain reaction malaria detection assay for epidemiologic studies. AmJTrop Med Hyg. 1999, 60: 687-692.\nBarker RH, Banchongaksorn T, Courval JM, Suwonkerd W, Rimwungtragoon K, Wirth DF: Plasmodium falciparum and P. vivax: factors affecting sensitivity and specificity of PCR-based diagnosis of malaria. Exp Parasitol. 1994, 79: 41-49. 10.1006\u002Fexpr.1994.1057.\nTham JM, Lee SH, Tan TM, Ting RC, Kara UA: Detection and species determination of malaria parasites by PCR: comparison with microscopy and with ParaSight-F and ICT malaria Pf tests in a clinical environment. J Clin Microbiol. 1999, 37: 1269-1273.\nMayxay M, Pukritrayakamee S, Chotivanich K, Imwong M, Looareesuwan S, White NJ: Identification of cryptic coinfection with Plasmodium falciparum in patients presenting with vivax malaria. AmJTrop Med Hyg. 2001, 65: 588-592.\nMueller I, Zimmerman PA, Reeder JC: Plasmodium malariae and Plasmodium ovale–the “bashful” malaria parasites. Trends Parasitol. 2007, 23: 278-283. 10.1016\u002Fj.pt.2007.04.009.\nZimmerman PA, Mehlotra RK, Kasehagen LJ, Kazura JW: Why do we need to know more about mixed Plasmodium species infections in humans?. Trends Parasitol. 2004, 20: 440-447. 10.1016\u002Fj.pt.2004.07.004.\nMueller I, Galinski MR, Baird JK, Carlton JM, Kochar DK, Alonso PL, del Portillo HA: Key gaps in the knowledge of Plasmodium vivax, a neglected human malaria parasite. Lancet Infect Dis. 2009, 9: 555-566. 10.1016\u002FS1473-3099(09)70177-X.\nPadley D, Moody AH, Chiodini PL, Saldanha J: Use of a rapid, single-round, multiplex PCR to detect malarial parasites and identify the species present. Ann Trop Med Parasitol. 2003, 97: 131-137. 10.1179\u002F000349803125002977.",{"VOID":1400},"10.1186\u002F1475-2875-11-119","https:\u002F\u002Fmalariajournal.biomedcentral.com\u002Farticles\u002F10.1186\u002F1475-2875-11-119",[1403,1418,1433,1446,1470,1483,1498,1518,1538],{"id":1404,"sortIndex":32,"researcher":28,"roles":1405,"affiliations":1406,"properties":1415,"displayName":1417,"givenName":28,"familyName":28},"96e0bfe0-f2e0-4e7f-b0a7-36ed94bfb11a",[1026],[1407],{"id":1408,"sortIndex":32,"affiliation":1409,"properties":28},"14bb71af-e058-46e2-b06a-82345bc1baf5",{"id":1408,"createTime":28,"updateTime":28,"relativeEntities":1410,"slug":28,"properties":1411,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1414,"statistic":28},[],{"title":1412},{"VI":1413},"MEIZ-Microbiology School, National Autonomous University of Honduras (UNAH), Tegucigalpa, Honduras",[],{"title":1416},{"VI":1417},"Gustavo A 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Mendoza",{"id":1434,"sortIndex":123,"researcher":28,"roles":1435,"affiliations":1436,"properties":1443,"displayName":1445,"givenName":28,"familyName":28},"3808d56e-5434-48dd-88eb-bf40e6a609c6",[1026],[1437],{"id":1423,"sortIndex":32,"affiliation":1438,"properties":28},{"id":1423,"createTime":28,"updateTime":28,"relativeEntities":1439,"slug":28,"properties":1440,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1442,"statistic":28},[],{"title":1441},{"VI":1428},[],{"title":1444},{"VI":1445},"Engels 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birds are frequently infected with diverse haemosporidian parasites. While infections are traditionally considered benign in wild birds, recent studies demonstrated mortalities of passerine species due to exo-erythrocytic development of the parasites, which can damage organs in affected hosts. However, exo-erythrocytic development remains insufficiently investigated for most haemosporidian species and thus little is known about the virulence of tissue stages in wild passerine birds. The aim of the present study was to investigate natural haemosporidian infections in deceased Eurasian blackbirds (Turdus merula) and song thrushes (Turdus philomelos) and to determine parasite burden and associated histological effects. For molecular analysis, blood and tissue samples from 306 thrushes were screened for Plasmodium, Haemoproteus and Leucocytozoon parasites by nested PCR. For the detection of parasite stages in organ samples, tissue sections were subjected to chromogenic in situ hybridization (CISH) using genus- and species-specific probes targeting the rRNAs of parasites. Exo-erythrocytic parasite burden was semi-quantitatively assessed and histological lesions were evaluated in haematoxylin–eosin-stained sections. By PCR, 179 of 277 Eurasian blackbirds and 15 of 29 song thrushes were positive for haemosporidians. Parasites of all three genera were detected, with Plasmodium matutinum LINN1 and Plasmodium vaughani SYAT05 showing the highest prevalence. CISH revealed significant differences in exo-erythrocytic parasite burden between lineages in Eurasian blackbirds, with P. matutinum LINN1 frequently causing high exo-erythrocytic parasite burdens in various organs that were associated with histological alterations. Song thrushes infected with P. matutinum LINN1 and birds infected with other haemosporidian lineages showed mostly low exo-erythrocytic parasite burdens. Two Eurasian blackbirds infected with Leucocytozoon sp. TUMER01 showed megalomeronts in various organs that were associated with inflammatory reactions and necroses. This study suggests that P. matutinum LINN1, a common lineage among native thrushes, regularly causes high exo-erythrocytic parasite burdens in Eurasian blackbirds, which may result in disease and mortalities, indicating its high pathogenic potential. The findings further illustrate that the same parasite lineage may show different levels of virulence in related bird species which should be considered when assessing the pathogenicity of haemosporidian parasite species. Finally, the study provides evidence of virulent Leucocytozoon sp. TUMER01 infections in two Eurasian blackbirds caused by megalomeront formation.",{"EN":1614},"Haemosporidioses in wild Eurasian blackbirds (Turdus merula) and song thrushes (T. philomelos): an in situ hybridization study with emphasis on exo-erythrocytic parasite burden",{"VOID":1616},"Valkiūnas G. Avian malaria parasites and other haemosporidia. 1st ed. Boca Raton: CRC Press; 2005.\nBensch S, Hellgren O, Pérez-Tris J. MalAvi: a public database of malaria parasites and related haemosporidians in avian hosts based on mitochondrial cytochrome b lineages. Mol Ecol Resour. 2009;9:1353–8.\nScheuerlein A, Ricklefs RE. Prevalence of blood parasites in European passeriform birds. Proc Biol Sci. 2004;271:1363–70.\nBraga EM, Silveira P, Belo NO, Valkiūnas G. Recent advances in the study of avian malaria: an overview with an emphasis on the distribution of Plasmodium spp in Brazil. Mem Inst Oswaldo Cruz. 2011;106(Suppl):3–11.\nBensch S, Stjernman M, Hasselquist D, Ostman O, Hansson B, Westerdahl H, et al. Host specificity in avian blood parasites: a study of Plasmodium and Haemoproteus mitochondrial DNA amplified from birds. Proc Biol Sci. 2000;267:1583–9.\nVentim R, Tenreiro P, Grade N, Encarnação P, Araújo M, Mendes L, et al. Characterization of haemosporidian infections in warblers and sparrows at south-western European reed beds. J Ornithol. 2012;153:505–12.\nKrižanauskienė A, Hellgren O, Kosarev V, Sokolov L, Bensch S, Valkiūnas G. Variation in host specificity between species of avian hemosporidian parasites: evidence from parasite morphology and cytochrome B gene sequences. J Parasitol. 2006;92:1319–24.\nVan Hemert C, Meixell BW, Smith MM, Handel CM. Prevalence and diversity of avian blood parasites in a resident northern passerine. Parasit Vectors. 2019;12:292.\nAtkinson CT, Dusek RJ, Lease JK. Serological responses and immunity to superinfection with avian malaria in experimentally-infected Hawaii amakihi. J Wildl Dis. 2001;37:20–7.\nDonovan TA, Schrenzel M, Tucker TA, Pessier AP, Stalis IH. Hepatic hemorrhage, hemocoelom, and sudden death due to Haemoproteus infection in passerine birds: eleven cases. J Vet Diagn Invest. 2008;20:304–13.\nHill AG, Howe L, Gartrell BD, Alley MR. Prevalence of Leucocytozoon spp, in the endangered yellow-eyed penguin Megadyptes antipodes. Parasitology. 2010;137:1477–85.\nTaunde PA, Bianchi MV, Perles L, da Silva FS, Guim TN, Stadler RA, et al. Pathological and molecular characterization of avian malaria in captive Magellanic penguins (Spheniscus magellanicus) in South America. Parasitol Res. 2019;118:599–606.\nVanstreels RET, Dutra DDA, Ferreira-Junior FC, Hurtado R, Egert L, Mayorga LFSP, et al. Epidemiology, hematology, and unusual morphological characteristics of Plasmodium during an avian malaria outbreak in penguins in Brazil. Parasitol Res. 2019;118:3497–508.\nDinhopl N, Mostegl MM, Richter B, Nedorost N, Maderner A, Fragner K, et al. Application of in situ hybridization for the detection and identification of avian malaria parasites in paraffin wax-embedded tissues from captive penguins. Avian Pathol. 2011;40:315–20.\nOlias P, Wegelin M, Zenker W, Freter S, Gruber AD, Klopfleisch R. Avian malaria deaths in parrots. Europe. Emerg Infect Dis. 2011;17:950–2.\nValkiūnas G, Pendl H, Olias P. New Haemoproteus parasite of parrots, with remarks on the virulence of haemoproteids in naive avian hosts. Acta Trop. 2017;176:256–62.\nOrtiz-Catedral L, Brunton D, Stidworthy MF, Elsheikha HM, Pennycott T, Schulze C, et al. Haemoproteus minutus is highly virulent for Australasian and South American parrots. Parasit Vectors. 2019;12:40.\nJia T, Huang X, Valkiūnas G, Yang M, Zheng C, Pu T, et al. Malaria parasites and related haemosporidians cause mortality in cranes: a study on the parasites diversity, prevalence and distribution in Beijing Zoo. Malar J. 2018;17:234.\nIlgūnas M, Bukauskaitė D, Palinauskas V, Iezhova TA, Dinhopl N, Nedorost N, et al. Mortality and pathology in birds due to Plasmodium (Giovannolaia) homocircumflexum infection, with emphasis on the exoerythrocytic development of avian malaria parasites. Malar J. 2016;15:256.\nDimitrov D, Palinauskas V, Iezhova TA, Bernotienė R, Ilgūnas M, Bukauskaitė D, et al. Plasmodium spp.: an experimental study on vertebrate host susceptibility to avian malaria. Exp Parasitol. 2015;148:1–16.\nIlgūnas M, Palinauskas V, Platonova E, Iezhova T, Valkiūnas G. The experimental study on susceptibility of common European songbirds to Plasmodium elongatum (lineage pGRW6), a widespread avian malaria parasite. Malar J. 2019;18:290.\nIlgūnas M, Bukauskaitė D, Palinauskas V, Iezhova T, Fragner K, Platonova E, et al. Patterns of Plasmodium homocircumflexum virulence in experimentally infected passerine birds. Malar J. 2019;18:174.\nPalinauskas V, Valkiūnas G, Bolshakov CV, Bensch S. Plasmodium relictum (lineage P-SGS1): effects on experimentally infected passerine birds. Exp Parasitol. 2008;120:372–80.\nRouffaer LO, Steensels M, Verlinden M, Vervaeke M, Boonyarittichaikij R, Martel A, et al. Usutu Virus epizootic and Plasmodium coinfection in Eurasian Blackbirds (Turdus merula) in Flanders, Belgium. J Wildl Dis. 2018;54:859–62.\nDinhopl N, Nedorost N, Mostegl MM, Weissenbacher-Lang C, Weissenböck H. In situ hybridization and sequence analysis reveal an association of Plasmodium spp. with mortalities in wild passerine birds in Austria. Parasitol Res. 2015;114:1455–62.\nHowe L, Castro IC, Schoener ER, Hunter S, Barraclough RK, Alley MR. Malaria parasites (Plasmodium spp.) infecting introduced, native and endemic New Zealand birds. Parasitol Res. 2012;110:913–23.\nValkiūnas G, Iezhova TA. Exo-erythrocytic development of avian malaria and related haemosporidian parasites. Malar J. 2017;16:101.\nHimmel T, Harl J, Kübber-Heiss A, Konicek C, Fernández N, Juan-Sallés C, et al. Molecular probes for the identification of avian Haemoproteus and Leucocytozoon parasites in tissue sections by chromogenic in situ hybridization. Parasit Vectors. 2019;12:282.\nMartínez J, Martínez-DE LA, Puente J, Herrero J, Del Cerro S, Lobato E, Rivero-DE Aguilar J, et al. A restriction site to differentiate Plasmodium and Haemoproteus infections in birds: on the inefficiency of general primers for detection of mixed infections. Parasitology. 2009;136:713–22.\nHellgren O, Waldenström J, Bensch S. A new PCR assay for simultaneous studies of Leucocytozoon, Plasmodium, and Haemoproteus from avian blood. J Parasitol. 2004;90:797–802.\nWeissenböck H, Kolodziejek J, Url A, Lussy H, Rebel-Bauder B, Nowotny N. Emergence of Usutu virus, an African mosquito-borne flavivirus of the Japanese encephalitis virus group, central Europe. Emerg Infect Dis. 2002;8:652–6.\nHall TA. BioEdit: a user-friendly biological sequences alignment editor and analysis program for Windows 95\u002F98\u002FNT. Nucleic Acids Symp Ser. 1999;41:95–8.\nRozas J, Ferrer-Mata A, Sánchez-DelBarrio JC, Guirao-Rico S, Librado P, Ramos-Onsins SE, et al. DnaSP 6: DNA Sequence polymorphism analysis of large data sets. Mol Biol Evol. 2017;34:3299–302.\nHarl J, Himmel T, Valkiūnas G, Weissenböck H. The nuclear 18S ribosomal DNAs of avian haemosporidian parasites. Malar J. 2019;18:305.\nHatchwell BJ, Wood MJ, Anwar M, Perrins CM. The prevalence and ecology of the haematozoan parasites of European blackbirds, Turdus merula. Can J Zool. 2000;78:684–7.\nBentz S, Rigaud T, Barroca M, Martin-Laurent F, Bru D, Moreau J, et al. Sensitive measure of prevalence and parasitaemia of haemosporidia from European blackbird (Turdus merula) populations: value of PCR-RFLP and quantitative PCR. Parasitology. 2006;133:685–92.\nCarbó-Ramírez P, Zuria I, Schaefer HM, Santiago-Alarcon D. Avian haemosporidians at three environmentally contrasting urban greenspaces. J Urban Ecol. 2017;3:1–11.\nHellgren O, Križanauskienė A, Hasselquist D, Bensch S. Low haemosporidian diversity and one key-host species in a bird malaria community on a mid-Atlantic island (São Miguel, Azores). J Wildl Dis. 2011;47:849–59.\nSchoener ER, Tompkins DM, Parker KA, Howe L, Castro I. Presence and diversity of mixed avian Plasmodium spp. infections in introduced birds whose distribution overlapped with threatened New Zealand endemic birds. N Z Vet J. 2019. https:\u002F\u002Fdoi.org\u002F10.1080\u002F00480169.2019.1680326.\nBernotienė R, Palinauskas V, Iezhova T, Murauskaitė D, Valkiūnas G. Avian haemosporidian parasites (Haemosporida): a comparative analysis of different polymerase chain reaction assays in detection of mixed infections. Exp Parasitol. 2016;163:31–7.\nValkiŭnas G, Bensch S, Iezhova TA, Krizanauskiené A, Hellgren O, Bolshakov CV. Nested cytochrome b polymerase chain reaction diagnostics underestimate mixed infections of avian blood haemosporidian parasites: microscopy is still essential. J Parasitol. 2006;92:418–22.\nValkiūnas G, Ilgūnas M, Bukauskaitė D, Palinauskas V, Bernotienė R, Iezhova TA. Molecular characterization and distribution of Plasmodium matutinum, a common avian malaria parasite. Parasitology. 2017. https:\u002F\u002Fdoi.org\u002F10.1017\u002FS0031182017000737.\nIezhova TA, Valkiūnas G, Bairlein F. Vertebrate host specificity of two avian malaria parasites of the subgenus Novyella: Plasmodium nucleophilum and Plasmodium vaughani. J Parasitol. 2005;91:472–4.\nRijks JM, Kik ML, Slaterus R, Foppen R, Stroo A, IJzer J, et al. Widespread Usutu virus outbreak in birds in the Netherlands, 2016. Euro Surveill. 2016;21:30391.\nBakonyi T, Erdélyi K, Brunthaler R, Dán Á, Weissenböck H, Nowotny N. Usutu virus, Austria and Hungary, 2010–2016. Emerg Microbes Infect. 2017;6:e85.\nManarolla G, Bakonyi T, Gallazzi D, Crosta L, Weissenböck H, Dorrestein GM, et al. Usutu virus in wild birds in northern Italy. Vet Microbiol. 2010;141:159–63.\nHöfle U, Gamino V, de Mera IGF, Mangold AJ, Ortíz J-A, de la Fuente J. Usutu virus in migratory song thrushes, Spain. Emerg Infect Dis. 2013;19:1173–5.\nHubálek Z, Rudolf I, Čapek M, Bakonyi T, Betášová L, Nowotny N. Usutu virus in blackbirds (Turdus merula), Czech Republic, 2011–2012. Transbound Emerg Dis. 2014;61:273–6.\nChvala S, Kolodziejek J, Nowotny N, Weissenböck H. Pathology and viral distribution in fatal Usutu virus infections of birds from the 2001 and 2002 outbreaks in Austria. J Comp Pathol. 2004;131:176–85.\nMeister T, Lussy H, Bakonyi T, Sikutová S, Rudolf I, Vogl W, et al. Serological evidence of continuing high Usutu virus (Flaviviridae) activity and establishment of herd immunity in wild birds in Austria. Vet Microbiol. 2008;127:237–48.\nCadar D, Lühken R, van der Jeugd H, Garigliany M, Ziegler U, Keller M, et al. Widespread activity of multiple lineages of Usutu virus, western Europe, 2016. Euro Surveill. 2017;22:1–7.\nWeidinger P, Kolodziejek J, Bakonyi T, Brunthaler R, Erdélyi K, Weissenböck H, et al. Different dynamics of Usutu virus infections in Austria and Hungary, 2017–2018. Transbound Emerg Dis. 2019. https:\u002F\u002Fdoi.org\u002F10.1111\u002Ftbed.13351.\nde Roode JC, Pansini R, Cheesman SJ, Helinski MEH, Huijben S, Wargo AR, et al. Virulence and competitive ability in genetically diverse malaria infections. Proc Natl Acad Sci USA. 2005;102:7624–8.\nBell AS, de Roode JC, Sim D, Read AF. Within-host competition in genetically diverse malaria infections: parasite virulence and competitive success. Evolution. 2006;60:1358–71.\nPalinauskas V, Valkiūnas G, Bolshakov CV, Bensch S. Plasmodium relictum (lineage SGS1) and Plasmodium ashfordi (lineage GRW2): the effects of the co-infection on experimentally infected passerine birds. Exp Parasitol. 2011;127:527–33.\nBehrens S, Fuchs BM, Mueller F, Amann R. Is the in situ accessibility of the 16S rRNA of Escherichia coli for Cy3-labeled oligonucleotide probes predicted by a three-dimensional structure model of the 30S ribosomal subunit? Appl Environ Microbiol. 2003;69:4935–41.\nFranke-Fayard B, Fonager J, Braks A, Khan SM, Janse CJ. Sequestration and tissue accumulation of human malaria parasites: can we learn anything from rodent models of malaria? PLoS Pathog. 2010;6:e1001032.\nCowman AF, Healer J, Marapana D, Marsh K. Malaria: biology and disease. Cell. 2016;167:610–24.\nIshak HD, Dumbacher JP, Anderson NL, Keane JJ, Valkiūnas G, Haig SM, et al. Blood parasites in owls with conservation implications for the Spotted Owl (Strix occidentalis). PLoS ONE. 2008;3:e2304.\nPadilla DP, Illera JC, Gonzalez-Quevedo C, Villalba M, Richardson DS. Factors affecting the distribution of haemosporidian parasites within an oceanic island. Int J Parasitol. 2017;47:225–35.",{"VOID":1618},"10.1186\u002Fs12936-020-3147-6","https:\u002F\u002Fmalariajournal.biomedcentral.com\u002Farticles\u002F10.1186\u002Fs12936-020-3147-6",[1621,1636,1649,1662,1675,1699],{"id":1622,"sortIndex":32,"researcher":28,"roles":1623,"affiliations":1624,"properties":1633,"displayName":1635,"givenName":28,"familyName":28},"15e79eaa-d26a-4d85-b193-9068acb76624",[1026],[1625],{"id":1626,"sortIndex":32,"affiliation":1627,"properties":28},"96bc4c2f-e933-49ed-8347-5e220820401d",{"id":1626,"createTime":28,"updateTime":28,"relativeEntities":1628,"slug":28,"properties":1629,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1632,"statistic":28},[],{"title":1630},{"VI":1631},"Department for Pathobiology, Institute of Pathology, University of Veterinary Medicine Vienna, Vienna, Austria",[],{"title":1634},{"VI":1635},"Tanja Himmel",{"id":1637,"sortIndex":40,"researcher":28,"roles":1638,"affiliations":1639,"properties":1646,"displayName":1648,"givenName":28,"familyName":28},"a12aab64-0da0-455f-b3f4-e9152e9b8929",[1026],[1640],{"id":1626,"sortIndex":32,"affiliation":1641,"properties":28},{"id":1626,"createTime":28,"updateTime":28,"relativeEntities":1642,"slug":28,"properties":1643,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1645,"statistic":28},[],{"title":1644},{"VI":1631},[],{"title":1647},{"VI":1648},"Josef 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Austria",[],{"id":1688,"sortIndex":40,"affiliation":1689,"properties":1695},"94622b65-cff2-41c0-935c-6d6a1e3b6bdc",{"id":1688,"createTime":28,"updateTime":28,"relativeEntities":1690,"slug":28,"properties":1691,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1694,"statistic":28},[],{"title":1692},{"VI":1693},"Department of Basic Medical Sciences, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates",[],{},{"title":1697},{"VI":1698},"Norbert Nowotny",{"id":1700,"sortIndex":46,"researcher":28,"roles":1701,"affiliations":1702,"properties":1709,"displayName":1711,"givenName":28,"familyName":28},"0987eebd-1c19-41e3-a6e0-59a22837c77c",[1026],[1703],{"id":1626,"sortIndex":32,"affiliation":1704,"properties":28},{"id":1626,"createTime":28,"updateTime":28,"relativeEntities":1705,"slug":28,"properties":1706,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1708,"statistic":28},[],{"title":1707},{"VI":1631},[],{"title":1710},{"VI":1711},"Herbert 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biết về bệnh sinh của sốt rét trong thai kỳ và những hậu quả của nó đối với cả mẹ và bé là điều cơ bản để cải thiện kiểm soát sốt rét ở phụ nữ mang thai. Nghiên cứu này nhằm điều tra vai trò của các nhóm máu ABO đối với các kết quả thai kỳ tại một khu vực có tỷ lệ truyền bệnh sốt rét không ổn định ở đông Sudan. Tổng cộng có 293 phụ nữ sinh con tại bệnh viện giảng dạy New Half, đông Sudan trong thời gian từ tháng 10 năm 2006 đến tháng 3 năm 2007 đã được phân tích. Các nhóm máu ABO được xác định và có các khám nghiệm mô bệnh lý nhau thai cho sốt rét được thực hiện. Cân nặng của trẻ sơ sinh và nhau thai đã được ghi nhận và nồng độ hemoglobin của mẹ cũng được đo. 114 (39.7%), 61 (22.1%) và 118 (38.2%) phụ nữ lần lượt là lần đầu sinh, sinh con thứ hai và đã sinh nhiều. Phân bố nhóm máu ABO là 82 (A), 59 (B), 24 (AB) và 128 (O). Mô bệnh học nhau thai cho thấy nhiễm khuẩn sốt rét cấp tính trong nhau thai ở 6 (2%), nhiễm khuẩn mãn tính ở 6 (2%), 82 (28.0%) nhau thai cho thấy nhiễm trùng trong quá khứ và 199 (68.0%) không cho thấy nhiễm trùng. Không có mối liên hệ nào giữa độ tuổi (OR = 1.02, 95% CI = 0.45–2.2; P = 0.9), số lần sinh (OR = 0.6, 95% CI = 0.3–1.2; P = 0.1) và nhiễm khuẩn sốt rét nhau thai. Trong tất cả các lần sinh, nhóm máu O có liên quan đến nguy cơ cao hơn của nhiễm khuẩn sốt rét nhau thai trong quá khứ (OR = 1.9, 95% CI = 1.1–3.2; P = 0.01). Điều này cũng đúng khi chỉ xem xét riêng phụ nữ lần đầu sinh (OR = 2.6, 95% CI = 1.05–6.5, P = 0.03). Trong số phụ nữ có tất cả các nhiễm trùng nhau thai\u002Fnhiễm trùng nhau thai trong quá khứ, nồng độ hemoglobin trung bình cao hơn ở phụ nữ thuộc nhóm máu O, nhưng cân nặng trung bình của trẻ sơ sinh, tỷ lệ cân nặng thai nhi-nhau thai không khác biệt giữa các nhóm này và nhóm không phải O. Những kết quả này cho thấy phụ nữ ở đông Sudan có nguy cơ mắc nhiễm khuẩn sốt rét nhau thai mà không phân biệt độ tuổi hoặc số lần sinh. Những phụ nữ có nhóm máu O có nguy cơ cao hơn của nhiễm khuẩn sốt rét nhau thai trong quá khứ.","Understanding the pathogenesis of malaria in pregnancy and its consequences for both the mother and the baby is fundamental for improving malaria control in pregnant women. The study aimed to investigate the role of ABO blood groups on pregnancy outcomes in an area of unstable malaria transmission in eastern Sudan. A total of 293 women delivering in New Half teaching hospital, eastern Sudan during the period October 2006–March 2007 have been analyzed. ABO blood groups were determined and placental histopathology examinations for malaria were performed. Birth and placental weight were recorded and maternal haemoglobin was measured. 114 (39.7%), 61 (22.1%) and 118 (38.2%) women were primiparae, secundiparae and multiparae, respectively. The ABO blood group distribution was 82(A), 59 (B), 24 (AB) and 128 (O). Placental histopathology showed acute placental malaria infections in 6 (2%), chronic infections in 6 (2%), 82 (28.0%) of the placentae showed past infection and 199 (68.0%) showed no infection. There was no association between the age (OR = 1.02, 95% CI = 0.45–2.2; P = 0.9), parity (OR = 0.6, 95% CI = 0.3–1.2; P = 0.1) and placental malaria infections. In all parity blood group O was associated with a higher risk of past (OR = 1.9, 95% CI = 1.1–3.2; P = 0.01) placental malaria infection. This was also true when primiparae were considered separately (OR = 2.6, 95% CI = 1.05–6.5, P = 0.03). Among women with all placental infections\u002Fpast placental infection, the mean haemoglobin was higher in women with the blood group O, but the mean birth weight, foeto-placental weight ratio was not different between these groups and the non-O group. These results indicate that women of eastern Sudan are at risk for placental malaria infection irrespective to their age or parity. Those women with blood group O were at higher risk of past placental malaria infection.",{"EN":1777,"VI":1778},"ABO blood group system and placental malaria in an area of unstable malaria transmission in eastern Sudan","Hệ thống nhóm máu ABO và sốt rét ở nhau thai trong khu vực có truyền bệnh sốt rét không ổn định ở đông Sudan",{"VI":1780},"sốt rét, thai kỳ, nhóm máu ABO, nhiễm khuẩn nhau thai, đông Sudan",{"VOID":1782},"Steketee RW, Nahlen BL, Parise MF, Menendez C: The burden of malaria in pregnancy in malaria-endemic areas. Am J Trop Med Hyg. 2001, 64 (Suppl): 28-35.\nCot M, Deloron P: Malaria during pregnancy: consequences and interventional perspectives. Med Trop. 2003, 63 (4-5): 369-380.\nAdam I, Khamis AH, Elbashir MI: Prevalence and risk factors for malaria in pregnant women of eastern Sudan. Malar J. 2005, 4: 8-10.1186\u002F1475-2875-4-18.\nAdam I, Khamis AH, Elbashir MI: Prevalence and risk factors for anaemia in pregnant women of eastern Sudan. Trans R Soc Trop Med Hyg. 2005, 90: 739-743. 10.1016\u002Fj.trstmh.2005.02.008.\nDafallah SE, EL-Agib FH, Bushra GO: Maternal mortality in a teaching hospital in Sudan. Saudi Med J. 2003, 24: 369-373.\nTaha Tel T, Gray RH, Mohamedani AA: Malaria and low birth weight in central Sudan. Am J Epidemiol. 1993, 138 (5): 315-325.\nCosta FT, Fusai T, Parzy D, Sterkers Y, Torrentino M, Douki JB, Traore B, Petres S, Scherf A, Gysin J: Immunization with recombinant duffy binding-like-gamma3 induces pan-reactive and adhesion-blocking antibodies against placental chondroitin sulfate A-binding Plasmodium falciparum parasites. J Infect Dis. 2003, 188: 153-164. 10.1086\u002F375800.\nCserti CM, Dzik WH: The ABO blood group system and Plasmodium falciparum malaria. Blood. 2007,\nBarragan A, Klremsssner PG, Wahlgre M, Carlson J: Blood group A antigen is a co-receptor in Plasmodium falciparum rosetting. Infect Immun. 2000, 68: 2971-2975. 10.1128\u002FIAI.68.5.2971-2975.2000.\nMaubert B, Fievet N, Tami G, Boudin C, Deloron P: Plasmodium falciparum-isolates from Cameroonian pregnant women do not rosette. Parasite. 1998, 5: 281-283.\nLoscertales MP, Brabin BJ: ABO phenotypes and malaria related outcomes in mothers and babies in The Gambia: a role for histo-blood groups in placental malaria. Malar J. 2006, 5: 72-10.1186\u002F1475-2875-5-72.\nHimeidan YE, Malik EM, Adam I: Epidemiology and seasonal pattern of malaria in an irrigated area of eastern Sudan. Am J Inf Dis. 2005, 1: 75-78.\nAdam I, Nour BY, Ibrahim EY, Almahi WA, Omer EM, Ali NY: Cortisol and susceptibility to malaria in pregnant women in an area of unstable malaria transmission in eastern Sudan. Intern J Gynecol Obstet. 2007,\nBulmer JN, Rasheed FN, Francis N, Morrison L, Greenwood BM: Placental malaria. I. Pathological classification. Histopathology. 1993, 22: 211-218. 10.1111\u002Fj.1365-2559.1993.tb00110.x.\nAdam I, AlElbasit IE, Salih I, Elbashir MI: Submicroscopic Plasmodium falciparum infections during pregnancy, in an area of Sudan with low malaria transmission. Ann Trop Med Parasitol. 2005, 99: 339-344. 10.1179\u002F136485905X36244.\nGiha HA, A-Elbasit IE, Elgadir TM, Adam I, Berzins K, Elghazali G, Ebashir MI: Cerebral malaria is frequently associated with latent parasitemia among the semi-immune population of eastern Sudan. Microbes Infect. 2005, 7: 1196-1203. 10.1016\u002Fj.micinf.2005.04.004.\nPathirana SL, Alles HK, Bandara S, Phone-Kyaw M, Perera MK, Wickremasinghe AR, Mendis KN, Handunnetti SM: ABO-blood-group types and protection against severe, Plasmodium falciparum malaria. Ann Trop Med Parasitol. 2005, 99: 119-124. 10.1179\u002F136485905X19946.\nUneke CJ: Plasmodium falciparum malaria and ABO blood group: is there any relationship?. Parasitol Res. 2007, 100: 759-765. 10.1007\u002Fs00436-006-0342-5.\nHimiedan YE, Elbashir MI, Adam I: Attractiveness of pregnant Sudanese women to malarial vector-Anopheles arabiensis. Ann Trop Med Parasitol. 2004, 98: 631-633. 10.1179\u002F000349804225021307.\nWood CS: Preferential feeding of Anopheles gambiae mosquitoes on human subjects of blood group O: A relationship between the ABO polymorphism and malaria vectors. Hum Biol. 1974, 46: 385-404.\nAthreya BH, Coriell L: Relation of blood groups to infection. I. A survey and review of data suggesting possible relationship between malaria and blood groups. Am J Epidemiol. 1967, 86: 292-304.\nPodbielska M, Fredriksson SA, Nilsson B, Lisowska E, Krotkiewski H: ABH blood group antigens in O-glycans of human glycophorin A. Arch Biochem Biophys. 2004, 429: 145-153. 10.1016\u002Fj.abb.2004.06.018.\nFischer PR, Boone P: Short report: severe malaria associated with blood group. Am J Trop Med Hyg. 1998, 58: 122-123.",{"VOID":1784},"10.1186\u002F1475-2875-6-110","2024-12-31T07:02:32.033+00:00",[30],"https:\u002F\u002Fmalariajournal.biomedcentral.com\u002Farticles\u002F10.1186\u002F1475-2875-6-110",[1789,1804,1819,1834,1849,1864],{"id":1790,"sortIndex":32,"researcher":28,"roles":1791,"affiliations":1792,"properties":1801,"displayName":1803,"givenName":28,"familyName":28},"da669e60-94fa-4fbc-a5d2-d0e333b44d49",[1026],[1793],{"id":1794,"sortIndex":32,"affiliation":1795,"properties":28},"fec83e3b-806f-4f81-a1bf-f62402659fd7",{"id":1794,"createTime":28,"updateTime":28,"relativeEntities":1796,"slug":28,"properties":1797,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1800,"statistic":28},[],{"title":1798},{"VI":1799},"Department of Obstetrics & Gynecology, Faculty of Medicine University of Khartoum, Sudan",[],{"title":1802},{"VI":1803},"Ishag Adam",{"id":1805,"sortIndex":40,"researcher":28,"roles":1806,"affiliations":1807,"properties":1816,"displayName":1818,"givenName":28,"familyName":28},"000f2e3f-d921-44fe-ad2b-d049c1a4e0e8",[1026],[1808],{"id":1809,"sortIndex":32,"affiliation":1810,"properties":28},"02cf4da1-ab36-42b1-9382-55cac9f96622",{"id":1809,"createTime":28,"updateTime":28,"relativeEntities":1811,"slug":28,"properties":1812,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1815,"statistic":28},[],{"title":1813},{"VI":1814},"Faculty Of Medical Technical Sciences, Alzaiem Alazharai University, Sudan",[],{"title":1817},{"VI":1818},"Saud Babiker",{"id":1820,"sortIndex":123,"researcher":28,"roles":1821,"affiliations":1822,"properties":1831,"displayName":1833,"givenName":28,"familyName":28},"cec73baa-4068-4450-a2ef-ef520f1612ff",[1026],[1823],{"id":1824,"sortIndex":32,"affiliation":1825,"properties":28},"1241addc-7f4f-452c-b0c7-f8e3d319928b",{"id":1824,"createTime":28,"updateTime":28,"relativeEntities":1826,"slug":28,"properties":1827,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1830,"statistic":28},[],{"title":1828},{"VI":1829},"Faculty of Medicine, Ribat University, Sudan",[],{"title":1832},{"VI":1833},"Ahmed A Mohmmed",{"id":1835,"sortIndex":42,"researcher":28,"roles":1836,"affiliations":1837,"properties":1846,"displayName":1848,"givenName":28,"familyName":28},"27fc40ad-7238-49fb-88a2-8fbfc8150e93",[1026],[1838],{"id":1839,"sortIndex":32,"affiliation":1840,"properties":28},"c50fe1da-eb21-469f-a387-3c3a2f498108",{"id":1839,"createTime":28,"updateTime":28,"relativeEntities":1841,"slug":28,"properties":1842,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1845,"statistic":28},[],{"title":1843},{"VI":1844},"Faculty of Medical Laboratory Sciences, University of Khartoum, Sudan",[],{"title":1847},{"VI":1848},"Magdi M Salih",{"id":1850,"sortIndex":45,"researcher":28,"roles":1851,"affiliations":1852,"properties":1861,"displayName":1863,"givenName":28,"familyName":28},"89d86afd-26d0-42a4-b1e3-a35b0a2cdcb2",[1026],[1853],{"id":1854,"sortIndex":32,"affiliation":1855,"properties":28},"5db87559-09b6-4692-a8f8-9a642cfdcd9e",{"id":1854,"createTime":28,"updateTime":28,"relativeEntities":1856,"slug":28,"properties":1857,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1860,"statistic":28},[],{"title":1858},{"VI":1859},"Department of Epidemiology, Care and Public Health Research Institute, University of Maastricht, The Netherlands",[],{"title":1862},{"VI":1863},"Martin H Prins",{"id":1865,"sortIndex":46,"researcher":28,"roles":1866,"affiliations":1867,"properties":1874,"displayName":1876,"givenName":28,"familyName":28},"7d31c793-b4ef-4e21-983d-958b0af50ef2",[1026],[1868],{"id":1794,"sortIndex":32,"affiliation":1869,"properties":28},{"id":1794,"createTime":28,"updateTime":28,"relativeEntities":1870,"slug":28,"properties":1871,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1873,"statistic":28},[],{"title":1872},{"VI":1799},[],{"title":1875},{"VI":1876},"Zaki M 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transmission in Senegal is highly stratified, from low in the dry north to moderately high in the moist south. In northern Senegal, along the Senegal River Valley and in the Ferlo semi-desert region, annual incidence is less than five cases per 1000 inhabitants. Many nomadic pastoralists have permanent dwellings in the Ferlo Desert and Senegal River Valley, but spend dry season in the south with their herds, returning north when the rains start, leading to a concern that this population could contribute to ongoing transmission in the north. A modified snowball sampling survey was conducted at six sites in northern Senegal to determine the malaria prevention and treatment seeking practices and parasite prevalence among nomadic pastoralists in the Senegal River Valley and the Ferlo Desert. Nomadic pastoralists aged 6 months and older were surveyed during September and October 2014, and data regarding demographics, access to care and preventive measures were collected. Parasite infection was detected using rapid diagnostic tests (RDTs), microscopy (thin and thick smears) and polymerase chain reaction (PCR). Molecular barcodes were determined by high resolution melting (HRM). Of 1800 participants, 61% were male. Sixty-four percent had at least one bed net in the household, and 53% reported using a net the night before. Only 29% had received a net from a mass distribution campaign. Of the 8% (142) who reported having had fever in the last month, 55% sought care, 20% of whom received a diagnostic test, one-third of which (n = 5) were reported to be positive. Parasite prevalence was 0.44% by thick smear and 0.50% by PCR. None of the molecular barcodes identified among the nomadic pastoralists had been previously identified in Senegal. While access to and utilization of malaria control interventions among nomadic pastoralists was lower than the general population, parasite prevalence was lower than expected and sheds doubt on the perception that they are a source of ongoing transmission in the north. The National Malaria Control Program is making efforts to improve access to malaria prevention and case management for nomadic populations.",{"EN":1940},"Malaria prevalence, prevention and treatment seeking practices among nomadic pastoralists in northern Senegal",{"VOID":1942},"Senegal Malaria Impact Evaluation Group. Evaluation of the impact of the scale-up of malaria control interventions on all-cause mortality in children under five years of age in Senegal, 2005–2010. https:\u002F\u002Fwww.pmi.gov\u002Fdocs\u002Fdefault-source\u002Fdefault-document-library\u002Fpmi-reports\u002Fsenegal-impact-evaluation-report_508.pdf?sfvrsn=12. 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Haptoglobin phenotype prevalence and cytokine profiles during Plasmodium falciparum infection in Dogon and Fulani ethnic groups living in Mali. Malar J. 2013;25(12):432.\nLuoni G, Verra F, Arcà B, Sirima BS, Troye-Blomberg M, Coluzzi M, Kwiatkowski D, Modiano D. Antimalarial antibody levels and IL4 polymorphism in the Fulani of West Africa. Genes Immun. 2001;2(7):411–4.\nMaiga B, Dolo A, Touré O, Dara V, Tapily A, Campino S, Sepulveda N, Corran P, Rockett K, Clark TG, Blomberg MT, Doumbo OK. Fc gamma receptor IIa-H131R polymorphism and malaria susceptibility in sympatric ethnic groups, Fulani and Dogon of Mali. Scand J Immunol. 2014;79(1):43–50.\nCherif MK, Sanou GS, Maiga B, Israelsson E, Ouédraogo AL, Bougouma EC, Diarra A, Ouédraogo A, Ouattara AS, Troye-Blomberg M, Dolo A, Cavanagh DR, Theisen M, Modiano D, Sirima SB, Nebié I. FcγRIIa polymorphism and anti-malaria-specific IgG and IgG subclass responses in populations differing in susceptibility to malaria in Burkina Faso. Scand J Immunol. 2012;75(6):606–13.\nCherif M, Amoako-Sakyi D, Dolo A, Pearson JO, Gyan B, Obiri-Yeboah D, Nebie I, Sirima SB, Doumbo O, Troye-Blomberg M, Bakary M. Distribution of FcγR gene polymorphisms among two sympatric populations in Mali: differing allele frequencies, associations with malariometric indices and implications for genetic susceptibility to malaria. Malar J. 2016;19(15):29.\nSmith C, Whittaker M. Malaria elimination without stigmatization: a note of caution about the use of terminology in elimination settings. Malar J. 2014;13:377.\nAkogun OB, Adesina AO, Njobdi S, Ogundahunsi O. Nomadic Fulani communities manage malaria on the move. Int Health. 2012;4(1):10–9.\nLindtjørn B, Alemu T, Bjorvatn B. Population growth, fertility, mortality and migration in drought prone areas in Ethiopia. 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transmission in most of Latin America can be considered as controlled. In such a scenario, parameters of baseline immunity to malaria antigens are of specific interest with respect to future malaria eradication efforts. A cross-sectional study was carried out in two indigenous population groups in Amazonas\u002FVenezuela. Data from the regional malaria documentation system were extracted and participants from the ethnic groups of the Guahibo (n = 180) and Piaroa (n = 295) were investigated for the presence of Plasmodium parasites and naturally acquired antibodies to Plasmodium falciparum antigens in serum. The GMZ2 vaccine candidate proteins MSP3 and GLURP were chosen as serological markers. The incidence of P. falcip arum in both communities was found to be less than 2%, and none of the participants harboured P. falciparum at the time of the cross-sectional. Nearly a quarter of the participants (111\u002F475; 23,4%) had positive antibody titres to at least one of the antigens. 53\u002F475 participants (11.2%) were positive for MSP3, and 93\u002F475 participants (19.6%) were positive for GLURP. High positive responses were detected in 36\u002F475 participants (7.6%) and 61\u002F475 participants (12.8%) for MSP3 and GLURP, respectively. Guahibo participants had significantly higher antibody titres than Piaroa participants. Considering the low incidence of P. falciparum, submicroscopical infections may explain the comparatively high anti-P. falciparum antibody concentrations.",{"EN":2165},"Naturally acquired immune responses to malaria vaccine candidate antigens MSP3 and GLURP in Guahibo and Piaroa indigenous communities of the Venezuelan Amazon",{"VOID":2167},"World Health Organization: The top 10 causes of death. Fact sheet N°310. (retrieved 21\u002F09\u002F2011), [http:\u002F\u002Fwww.who.int\u002Fmediacentre\u002Ffactsheets\u002Ffs310\u002Fen\u002Findex.html]\nMetzger WG, Giron AM, Vivas-Martínez S, González J, Charrasco AJ, Mordmüller BG, Magris M: A rapid malaria appraisal in the Venezuelan Amazon. Malar J. 2009, 8: 291-10.1186\u002F1475-2875-8-291.\nMetzger WG, Vivas-Martínez S, Rodriguez I, Gonçalves J, Bongard E, Fanello CI, Vivas L, Magris M: Malaria diagnosis under field conditions in the Venezuelan Amazon. Trans R Soc Trop Med Hyg. 2008, 102: 20-24. 10.1016\u002Fj.trstmh.2007.08.007.\nMetzger WG, Vivas-Martínez S, Giron A, Vaccari E, Campos E, Rodríguez I, Miranda E, Terán E, Olivio L, Magris M: Assessment of routine malaria diagnosis in the Venezuelan Amazon. Trans R Soc Trop Med Hyg. 2011, 105: 262-268. 10.1016\u002Fj.trstmh.2011.01.002.\nSmith DL, Klein EY, McKenzie FE, Laxminarayan R: Prospective strategies to delay the evolution of anti-malarial drug resistance: weighing the uncertainty. Malar J. 2010, 9: 217-10.1186\u002F1475-2875-9-217.\nMordmüller B: New medicines for malaria. Wien Klin Wochensch. 2010, 122 (Suppl 1): 19-22.\nEsen M, Kremsner PG, Schleucher R, Gässler M, Imoukhuede EB, Imbault N, Leroy O, Jepsen S, Knudsen BW, Schumm M, Knobloch J, Theisen M, Mordmüller B: Safety and immunogenicity of GMZ2 - a MSP3-GLURP fusion protein malaria vaccine candidate. Vaccine. 2009, 27: 6862-6868. 10.1016\u002Fj.vaccine.2009.09.011.\nMordmüller B, Szywon K, Greutelaers B, Esen M, Mewono L, Treut C, Mürbeth RE, Chilengi R, Noor R, Kilama WL, Imoukhuede EB, Imbault N, Leroy O, Theisen M, Jepsen S, Milligan P, Fendel R, Kremsner PG, Issifou S: Safety and immunogenicity of the malaria vaccine candidate GMZ2 in malaria-exposed, adult individuals from Lambaréné, Gabon. Vaccine. 2010, 28: 6698-6703. 10.1016\u002Fj.vaccine.2010.07.085.\nCarvalho LJM, Oliveira SG, Theisen M, Alves FA, Andrade MCR, Zanini GM, Soe S, Druilhe P, Theisen M, Muniz JAPC, Daniel-Ribeiro CT: Immunization of Saimiri sciureus monkeys with Plasmodium falciparu merozoite surface protein-3 and glutamate-rich protein suggests that protection is related to antibody levels. Scand J Immunol. 2004, 59: 363-372. 10.1111\u002Fj.0300-9475.2004.01409.x.\nBarry AE, Schultz L, Buckee CO, Reeder JC: Contrasting population structures of the genes encoding ten leading vaccine-candidate antigens of the human malaria parasite, Plasmodium falciparu. PLoS ONE. 2009, 4: e8497-10.1371\u002Fjournal.pone.0008497.\nFowkes FJI, Richards JS, Simpson JA, Beeson JG: The relationship between anti-merozoite antibodies and incidence of Plasmodium falciparu malaria: A systematic review and meta-analysis. PLoS Med. 2010, 7: e1000218-10.1371\u002Fjournal.pmed.1000218.\nBousema T, Youssef RM, Cook J, Cox J, Alegana VA, Amran J, Noor AM, Snow RW, Drakeley C: Serologic markers for detecting malaria in areas of low endemicity, Somalia, 2008. Emerging Infect Dis. 2010, 16: 392-399.\nGrenfell P, Fanello CI, Magris M, Goncalves J, Metzger WG, Vivas-Martínez S, Curtis C, Vivas L: Anaemia and malaria in Yanomami communities with differing access to healthcare. Trans R Soc Trop Med Hyg. 2008, 102: 645-652. 10.1016\u002Fj.trstmh.2008.02.021.\nKilian AH, Metzger WG, Mutschelknauss EJ, Kabagambe G, Langi P, Korte R, von Sonnenburg F: Reliability of malaria microscopy in epidemiological studies: results of quality control. Trop Med Int Health. 2000, 5: 3-8. 10.1046\u002Fj.1365-3156.2000.00509.x.\nTheisen M, Vuust J, Gottschau A, Jepsen S, Høgh B: Antigenicity and immunogenicity of recombinant glutamate-rich protein of Plasmodium falciparu expressed in Escherichia col. Clin Diagn Lab Immunol. 1995, 2: 30-34.\nBorre MB, Dziegiel M, Høgh B, Petersen E, Rieneck K, Riley E, Meis JF, Aikawa M, Nakamura K, Harada M: Primary structure and localization of a conserved immunogenic Plasmodium falcipar m glutamate rich protein (GLURP) expressed in both the preerythrocytic and erythrocytic stages of the vertebrate life cycle. Mol Biochem Parasitol. 1991, 49: 119-131. 10.1016\u002F0166-6851(91)90135-S.\nAudran R, Cachat M, Lurati F, Soe S, Leroy O, Corradin G, Druilhe P, Spertini F: Phase I malaria vaccine trial with a long synthetic peptide derived from the merozoite surface protein 3 antigen. Infect Immun. 2005, 73: 8017-8026. 10.1128\u002FIAI.73.12.8017-8026.2005.\nTheisen M, Soe S, Oeuvray C, Thomas AW, Vuust J, Danielsen S, Jepsen S, Druilhe P: The glutamate-rich protein (GLURP) of Plasmodium falciparu is a target for antibody-dependent monocyte-mediated inhibition of parasite growth in vitro. Infect Immun. 1998, 66: 11-17.\nMetzger WG, Okenu DMN, Cavanagh DR, Robinson JV, Bojang KA, Weiss HA, McBride JS, Greenwood BM, Conway DJ: Serum IgG3 to the Plasmodium falciparu merozoite surface protein 2 is strongly associated with a reduced prospective risk of malaria. Parasite Immunol. 2003, 25: 307-312. 10.1046\u002Fj.1365-3024.2003.00636.x.\nMetzger WG, Haywood M, D'Alessandro U, Drakeley CJ, Weiss H, Bojang K, Target GA, Greenwood BM: Serological responses of Gambian children to immunization with the malaria vaccine SPf66. Parasite Immunol. 1999, 21: 335-340. 10.1046\u002Fj.1365-3024.1999.00231.x.\nOvering J: The aesthetics of production: the sense of community among the Cubeo and Piaroa. Dialect Anthropol. 1989, 14: 159-175.\nMetzger DJ, Morey RV: Los Hiwis. Los Aborígenes de Venezuela. Edited by: Coppens W. 1983, Caracas: Instituto Caribe de Antropología, 2: 125-128.\nSojo-Milano M, Grande-Montalvo T: Epidemiologia de casos repetidores de Malaria en Amazonas, Venezuela. Boletín de Malariología y Salud Ambiental. 2009, 49: 73-89.\nGreenwood BM, Groenendaal F, Bradley AK, Greenwood AM, Shenton F, Tulloch S, Hayes R: Ethnic differences in the prevalence of splenomegaly and malaria in The Gambia. Ann Trop Med Parasitol. 1987, 81: 345-354.\nArama C, Giusti P, Boström S, Dara V, Traore B, Dolo A, Doumbo O, Varani S, Troye-Blomberg M: Interethnic differences in antigen-presenting cell activation and TLR responses in Malian children during Plasmodium falciparu malaria. PLoS One. 2011, 6: e18319-10.1371\u002Fjournal.pone.0018319.\nMarsh K, Hayes RH, Carson DC, Otoo L, Shenton F, Byass P, Zavala F, Greenwood BM: Anti-sporozoite antibodies and immunity to malaria in a rural Gambian population. Trans R Soc Trop Med Hyg. 1988, 82: 532-537. 10.1016\u002F0035-9203(88)90495-6.\nMetzger WG, Maxwell CA, Curtis CF: Anti-sporozoite immunity and impregnated bednets in Tanzanian villages. Ann Trop Med Parasitol. 1998, 92: 727-729. 10.1080\u002F00034989859195.\nRodríguez I, de Abreu N, Carrasquel A, Bolívar J, González M, Scorza JV, Pérez H: Infecciones maláricas en individuos asintomáticos en la población indígena Jivi, Amazonas, Venezuela. Boletín de Malariología y Salud Ambiental. 2010, 50: 197-205.\nChuangchaiya S, Jangpatarapongsa K, Chootong P, Sirichaisinthop J, Sattabongkot J, Pattanapanyasat K, Chotivanich K, Troye-Blomberg M, Cui L, Udomsangpetch R: Immune response to Plasmodium viva has a potential to reduce malaria severity. 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use pyrimethamine as an alternative anti-malarial drug for chloroquine-resistant malaria parasites, it was necessary to determine the enzyme's genetic variation in dihydrofolate reductase-thymidylate syntase (DHFR-TS) among Korean strains. Genetic variation of dhfr-ts genes of Plasmodium vivax clinical isolates from patients who did not respond to drug treatment (n = 11) in Korea were analysed. The genes were amplified using the polymerase chain reaction (PCR) with genomic DNA as a template. Sequence analysis showed that the open reading frame (ORF) of 1,857 nucleotides encoded a deduced protein of 618 amino acids (aa). Alignment with the DHFR-TS genes of other malaria parasites showed that a 231-residue DHFR domain and a 286-residue TS domain were seperated by a 101-aa linker region. This ORF shows 98.7% homology with the P. vivax Sal I strain (XM001615032) in the DHFR domain, 100% in the linker region and 99% in the TS domain. Comparison of the DHFR sequences from pyrimethamine-sensitive and pyrimethamine-resistant P. vivax isolates revealed that nine isolates belonged to the sensitive strain, whereas two isolates met the criteria for resistance. In these two isolates, the amino acid at position 117 is changed from serine to asparagine (S117N). Additionally, all Korean isolates showed a deletion mutant of THGGDN in short tandem repetitive sequences between 88 and 106 amino acid. These results suggest that sequence variations in the DHFR-TS represent the prevalence of antifolate-resistant P. vivax in Korea. Two of 11 isolates have the Ser to Asn mutation in codon 117, which is the major determinant of pyrimethamine resistance in P. vivax. Therefore, the introduction of pyrimethamine for the treatment of chloroquine-resistant vivax malaria as alternative drug in Korea should be seriously considered.",{"EN":2401},"Analysis of the dihydrofolate reductase-thymidylate synthase gene sequences in Plasmodium vivax field isolates that failed chloroquine treatment",{"VOID":2403},"Mendis K, Sina BJ, Marchesini P, Carter R: The neglected burden of Plasmodium vivax malaria. Am J Trop Med Hyg. 2001, 64: 97-106.\nNational Malaria Eradication Service, Ministry of Health and Social Affairs, ROK: Malaria pre-eradication programme in Korea, 1961-1965. Progress report. 1966, 44-70.\nPaik YH, Rhee HI, Shim JC: Malaria in Korea. Jpn J Exp Med. 1988, 58: 55-66.\nSoh CT, Lee KT, Im KI, Min DY, Ahn MH, Kim JJ, Yong TS: Current status of malaria in Korea. Yonsei Rep Trop Med. 1985, 16: 11-18.\nChai IH, Lim GI, Yoon SN, Oh WI, Kim SJ, Chai JY: Occurrence of tertian malaria in a male patient who has never been abroad. Korean J Parasitol. 1994, 32: 195-200. 10.3347\u002Fkjp.1994.32.3.195.\nCho SY, Kong Y, Park SM, Lee JS, Lim YA, Chae SL, Kho WG, Lee JS, Shim JC, Shin HK: Two vivax malaria cases detected in Korea. Korean J Parasitol. 1994, 32: 281-284. 10.3347\u002Fkjp.1994.32.4.281.\nLee JS, Kho WG, Lee HW, Seo M, Lee WJ: Current status of vivax malaria among civilians in Korea. Korean J Parasitol. 1998, 36: 241-248. 10.3347\u002Fkjp.1998.36.4.241.\nBaird JK, Basri H, Bangs MJ, Subianto B, Patchen LC, Hoffman SL: Resistance to chloroquine by Plasmodium vivax in Irian Jaya, Indonesia. Am J Trop Med Hyg. 1991, 44: 547-552.\nSchwartz IK, Lackrtiz EM, Patchen LC: Choroquine resistance Plasmodium vivax from Indonesia. N Engl J Med. 1991, 324: 927-10.1056\u002FNEJM199104113241506.\nGarg M, Gopinathan N, Bodhe P, Kshirsagar NA: Vivax malaria resistance to chloroquine: case reports from Bombay. Trans R Soc Trop Med Hyg. 1995, 89: 656-657. 10.1016\u002F0035-9203(95)90432-8.\nThan M, Kyaw MP, Soe AY, Gyi KK, Myint-Oo MS: Development of resistance to chloroquine by Plasmodium vivax in Myanmar. Trans R Soc Trop Med Hyg. 1995, 89: 307-308. 10.1016\u002F0035-9203(95)90556-1.\nFryauff DJ, Tuti S, Mardi A, Masbar S, Patipelohi R, Leksana B, Kain KC, Bangs MJ, Richie TL, Baird JK: Chloroquine-resistant Plasmodium vivax in transmigration settlements of West Kalimantan, Indonesia. Am J Trop Med Hyg. 1998, 59: 513-518.\nRuebush TK, Zegarra J, Cairo J, Andersen EM, Green M, Pillai DR, Marquino W, Huilca M, Arevalo E, Garcia C, Solary L, Kain KC: Chloroquine-resistant Plasmodium vivax malaria in Peru. Am J Trop Med Hyg. 2003, 69: 548-552.\nLuzzi GA, Warrell DA, Barnes AJ, Dunbar EM: Treatment of primaquine-resistant Plasmodium vivax malaria. Lancet. 1992, 340: 310-10.1016\u002F0140-6736(92)92404-4.\nWhite NJ: Assessment of the pharmacodynamic properties of antimalarial drugs in vivo. Antimicrob Agents Chemother. 1997, 41: 1413-1422.\nPukrittayakamee S, Chantra A, Simpson JA, Vanijanonta S, Clemens R, Looareesuwan S, White NJ: Therapeutic responses to different antimalarial drugs in vivax malaria. Antimicrob Agents Chemother. 2000, 44: 1680-1685. 10.1128\u002FAAC.44.6.1680-1685.2000.\nde Pécoulas PE, Basco LK, Tahar R, Ouatas T, Mazabraud A: Analysis or the Plasmodium vivax dihydrofolate reductase-thymidylate synthase gene sequence. Gene. 1998, 211: 177-185. 10.1016\u002FS0378-1119(98)00118-8.\nPeterson DS, Walliker D, Wellems TE: Evidence that a point mutation in dihydrofolate reductase-thymidylate synthase confers resistance to pyrimethamine in falciparum malaria. Proc Natl Acad Sci USA. 1988, 85: 9114-9118. 10.1073\u002Fpnas.85.23.9114.\nde Pécoulas PE, Basco LK, Le Bras J, Mazabraud A: Association between antifolate resistance in vitro and DHFR gene point mutation in Plasmodium falciparum isolates. Trans R Soc Trop Med Hyg. 1996, 90: 181-182. 10.1016\u002FS0035-9203(96)90130-3.\nBerens N, Schwoebel B, Jordan S, Vanisaveth V, Phetsouvanh R, Christophel EM, Phompida S, Jelinek T: Plasmodium falciparum: correlation of in vivo resistance to chloroquine and antifolates with genetic polymorphisms in isolates from the south of Lao PDR. Trop Med Int Health. 2003, 8: 775-782. 10.1046\u002Fj.1365-3156.2003.01099.x.\nKhalil I, Ronn AM, Alifrangis M, Gabar HA, Satti GM, Bygbjerg IC: Dihydrofolate reductase and dihydropteroate synthase genotypes associated with in vitro resistance of Plasmodium falciparum to pyrimethamine, trimethoprim, sulfadoxine, and sulfamethoxazole. Am J Trop Med Hyg. 2003, 68: 586-589.\nSirawaraporn W, Sirawaraporn R, Yongkiettrakul S, Anuwatwora A, Rastelli G, Kamchonwongpaisan S, Yuthavong Y: Mutational analysis of Plasmodium falciparum dihydrofolate reductase: the role of aspartate 54 and phenylalanine 223 on catalytic activity and antifolate binding. Mol Biochem Parasitol. 2002, 121: 185-193. 10.1016\u002FS0166-6851(02)00035-X.\nde Pécoulas PE, Tahar R, Ouatas T, Mazabraud A, Basco LK: Sequence variation in the Plasmodium vivax dihydrofolate reductase-thymylate synthase gene and their relationship with pyrimethamine resistance. Mol Biochem Parasitol. 1998, 92: 265-273. 10.1016\u002FS0166-6851(97)00247-8.\nImwong M, Pukrittakayamee S, Looareesuwan S, Pasvol G, Poirreiz J, White NJ, Snounou G: Association of genetic mutations in Plasmodium vivax dhfr with resistance to sulfadoxine-pyrimethamine: geographical and clinical correlates. Antimicrob Agents Chemother. 2001, 45: 3122-3127. 10.1128\u002FAAC.45.11.3122-3127.2001.\nde Pécoulas PE, Tahar R, Yi Poravuth, Thai KH, Basco LK: Genetic variation of the dihydrofolate reductase gene in Plasmodium vivax in Snoul, northeastern Cambodia. 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