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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. 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Rec., 84, 476, 10.1136\u002Fvr.84.19.476","https:\u002F\u002Fdoi.org\u002F10.1136\u002Fvr.84.19.476",{"mag":809,"openalex":810,"pm":811,"doi":812},"1999724723","W1999724723","4978564","10.1136\u002Fvr.84.19.476",{"id":26,"text":814,"url":26,"identifiers":815},"Curtin, 1961, Pseudomonas bacteremia: a review of ninety-one cases, Ann. Intern. Med., 54, 1077, 10.7326\u002F0003-4819-54-6-1077",{"doi":816},"10.7326\u002F0003-4819-54-6-1077",{"id":26,"text":818,"url":819,"identifiers":820},"Parmer, 1982, Hospital outbreaks caused by Pseudomonas aeruginosa: Importance of serogroup 011, J. Clin. Microbiol., 16, 266, 10.1128\u002FJCM.16.2.266-270.1982","http:\u002F\u002Fdx.doi.org\u002F10.1128\u002Fjcm.16.2.266-270.1982",{"doi":821},"10.1128\u002Fjcm.16.2.266-270.1982",{"id":26,"text":823,"url":26,"identifiers":824},"Fiereo, 1967, Pseudomonas aeruginosa traced to delivery-room resuscitators, New Engl. J. 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Ass., 180, 2188, 10.1001\u002Fjama.1959.63010180008012","https:\u002F\u002Fdoi.org\u002F10.1093\u002Fajhp\u002F16.12.734",{"mag":838,"openalex":839,"doi":840},"2908381891","W2908381891","10.1093\u002Fajhp\u002F16.12.734",{"id":26,"text":842,"url":843,"identifiers":844},"Godfrey, 1981, B-Lactam-resistant Pseudomonas aeruginosa with modified penicillin-binding proteins emerging during cystic fibrosis treatment, Antimicrob. Agents Chemother., 19, 705, 10.1128\u002FAAC.19.5.705","http:\u002F\u002Fdx.doi.org\u002F10.1128\u002Faac.19.5.705",{"doi":845},"10.1128\u002Faac.19.5.705",{"id":26,"text":847,"url":26,"identifiers":848},"Hoadley, 1968, Untersuchungen über Pseudomonas aeruginosa in Oberflächengewässern. I. Quellen, Arch. Hyg. Bakt., 152, 328",{},{"id":26,"text":850,"url":26,"identifiers":851},"Hugh, 1980, Pseudomonas, 288",{},{"id":26,"text":853,"url":26,"identifiers":854},"Kefalides, 1962, Role of infection in mortality from severe burns. Evaluation of plasma gamma-globulin, albumin and saline-solution therapy in a group of Peruvian children, New Engl. J. Med., 267, 317, 10.1056\u002FNEJM196208162670701",{"doi":855},"10.1056\u002FNEJM196208162670701",{"id":26,"text":857,"url":26,"identifiers":858},"Kim, 1983, Serotyping of Pseudomonas aeruginosa isolated from diseased chickens, Korean J. Vet. Publ. Hlth, 7, 1",{},{"id":782,"text":860,"url":784,"identifiers":861},"Kiss, 1983, Incidence of Pseudomonas aeruginosa serogroups in drinking water: use of serotyping in the control of water supplies, Acta Microbiol. Hung., 30, 131",{"doi":786},{"id":782,"text":863,"url":784,"identifiers":864},"Lusis, 1971, Pseudomonas aeruginosa, Vet. Bull. (Lond.), 41, 169",{"doi":786},{"id":26,"text":866,"url":26,"identifiers":867},"Magyar Ne’pkoztars-a-sa’gi. Orszagos Szabvany. Msz. 22901-71",{},{"id":782,"text":869,"url":784,"identifiers":870},"Maresz-Babczyszym, 1979, Biological properties of Pseudomonas aeruginosa strains isolated from surgical and burn wounds in hospitalized patients, Med. dośw. Mikrobiol., 31, 217",{"doi":786},{"id":26,"text":872,"url":873,"identifiers":874},"Markley, 1967, Immunotherapy of Pseudomonas infections, Ann. Intern. Med., 66, 443, 10.7326\u002F0003-4819-66-2-443","https:\u002F\u002Fdoi.org\u002F10.7326\u002F0003-4819-66-2-443",{"mag":875,"openalex":876,"pm":877,"doi":878},"2052899167","W2052899167","6016555","10.7326\u002F0003-4819-66-2-443",{"id":26,"text":880,"url":26,"identifiers":881},"Meitert, 1980, Investigation of epidemiological markers of Ps. aeruginosa strains isolated in animals. (In Romania), Ann. Sci. Sess. Cantacuzino Inst., 18, 99",{},{"id":782,"text":883,"url":784,"identifiers":884},"Meitert, 1980, Phage and serologic typing of Pseudomonas aeruginosa isolated in animals, Arch. roum. Path. exp. Microbiol., 39, 287",{"doi":786},{"id":26,"text":886,"url":26,"identifiers":887},"Muller, 1976, 229",{},{"id":26,"text":889,"url":26,"identifiers":890},"Nabbut, 1974, Pseudomonas aeruginosa serotypes encountered in the American University Hospital (AUB), Beirut, Lebanon, Leb. Med. J., 27, 695",{},{"id":26,"text":892,"url":26,"identifiers":893},"Postic, 1978, Contamination with Pseudomonas aeruginosa during fiberoptic bronchoscopy. Value of epidemiological markers, Med. Mal. Infect., 8, 92, 10.1016\u002FS0399-077X(78)80090-0",{"doi":894},"10.1016\u002FS0399-077X(78)80090-0",{"id":26,"text":896,"url":26,"identifiers":897},"Sanchez-Buen a ventura, 1977, The distribution of serotypes of Pseudomonas aeruginosa in the province of Valencia, Med. Esp., 76, 311",{},{"id":26,"text":899,"url":900,"identifiers":901},"Sausker, 1978, Pseudomonas folliculitis acquired from a health spa whirl-pool, J. Amer. med. 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Immunol., 24, 233, 10.1111\u002Fj.1348-0421.1980.tb00582.x","https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1348-0421.1980.tb00582.x",{"mag":916,"openalex":917,"pm":918,"doi":919},"1989463732","W1989463732","6774206","10.1111\u002Fj.1348-0421.1980.tb00582.x",false,{"id":922,"createTime":923,"updateTime":924,"relativeEntities":925,"slug":926,"properties":927,"entityType":696,"verifyStatus":25,"verifyTime":924,"verifyNote":698,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"primaryUrl":934,"fullTextUrl":26,"authors":935,"publicationType":755,"publisherRelationship":963,"citationCount":26,"citationInfo":26,"publishDate":982,"publishYear":983,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":26,"isForceReanalyzing":920},"97d1d224-7250-45c6-991f-8dd9a2ae1480","2023-12-25T11:04:09.115+00:00","2025-01-11T00:50:04.197+00:00",[],"Production-of-broad-spectrum-bacteriocin-like-activity-by-group-A-streptococci-of-particular-M-types",{"references":928,"title":930,"doi":932},{"VOID":929},"Johnson, 1979, Production of a bacteriocine-like substance by group-A streptococci of M-type 4 and T-pattern 4, J. Med. Microbiol., 12, 413, 10.1099\u002F00222615-12-4-413\nLütticken, 1976, Application of a new method for detecting streptococcal nicotinamide adenine dinucleotide glycohydrolase to various M-types of Streptococcus pyogenes, J. Clin. Microbiol., 3, 533, 10.1128\u002Fjcm.3.5.533-536.1976\nMaxted, 1973, The use of the serum opacity reaction in the typing of group-A streptococci, J. Med. Microbiol., 6, 83, 10.1099\u002F00222615-6-1-83\nOfek, 1971, Application of enzyme production properties in subtyping of group A streptococci according to T type, Appl. Microbiol., 22, 748, 10.1128\u002FAEM.22.5.748-751.1971\nSimpson, 1983, M-type 57 group A streptococcus bacteriocin, Canad. J. Microbiol., 29, 1445, 10.1139\u002Fm83-221\nSimpson, 1984, Survey of the plasmid content of group A streptococci, FEMS Microbiol. Lett., 23, 195, 10.1111\u002Fj.1574-6968.1984.tb01062.x\nSokol, 1979, A more sensitive plate assay for detection of protease production by Pseudomonas aeruginosa, J. Clin. Microbiol., 9, 538, 10.1128\u002Fjcm.9.4.538-540.1979\nTagg, 1984, Production of bacteriocin-like inhibitors by group A streptococci of nephritogenic M types, J. Clin. Microbiol., 19, 884, 10.1128\u002FJCM.19.6.884-887.1984\nTagg, 1979, “Fingerprinting” β-haemolytic streptococci by their production of and sensitivity to bacteriocine-like inhibitors, J. Med. Microbiol., 12, 397, 10.1099\u002F00222615-12-4-397\nTagg, 1983, Inhibitor production by group-G streptococci of human and of animal origin, J. Med. Microbiol., 16, 409, 10.1099\u002F00222615-16-4-409\nTagg, 1984, Evaluation of a typing scheme for group A streptococci based upon bacteriocin-like inhibitor production, Zbl. Bakt. Hyg., A257, 60\nTagg, 1976, Bacteriocins of Gram-positive bacteria, Bact. Rev., 40, 722, 10.1128\u002Fbr.40.3.722-756.1976\nTagg, 1971, Assay system for bacteriocins, Appl. 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Microbiol., 25, 146, 10.1128\u002FJCM.25.1.146-149.1987\nCzirók, 1976, The role in sporadic enteritis of facultatively enteropathogenic Escherichia coli serogroup, Acta Microbiol. Acad. Sci. Hung., 23, 359\nCzirók, 1985, Virulence factors of Escherichia coli. II. Antigens 04, 06 and 08, haemolysin production and mannose resistant haemagglutinating capacity are closely associated, Acta Microbiol. Hung., 32, 183\nDominque, 1985, Pathogenic significance of P- fimbriated Escherichia coli in urinary tract infections, J. Urol., 133, 983, 10.1016\u002FS0022-5347(17)49341-4\nEvans, 1977, Hemagglutination of human group A erythrocytes by enterotoxigenic Escherichia coli isolated from adults with diarrhea: correlation with colonization factor, Infect. Immun., 18, 330, 10.1128\u002FIAI.18.2.330-337.1977\nEvans, 1979, Hemagglutination patterns of enterotoxigenic and enteropathogenic Escherichia coli determined with human, bovine, chicken, and guinea-pig erythrocytes in the presence and absence of mannose, Infect. Immun., 23, 336, 10.1128\u002FIAI.23.2.336-346.1979\nEvans, 1980, Lethality of bacteremia-associated Escherichia coli for mice in relation to serotype and hemagglutination (HA)-type, FEMS Microbiol, Lett., 9, 171\nEvans, 1980, Definition of seven hemagglutination types, J. Clin. Microbiol., 12, 235, 10.1128\u002FJCM.12.2.235-242.1980\nEvans, 1981, Hemolysis and K antigens in relation to serotype and hemagglutination type of Escherichia coli isolated from extraintestinal infections, J. Clin. Microbiol., 13, 171, 10.1128\u002FJCM.13.1.171-178.1981\nGaastra, 1982, Host-specific fimbrial adhesins of non invasive enterotoxigenic Escherichia coli strains, Microbiol. 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Dis., 137, 648, 10.1093\u002Finfdis\u002F137.5.648\nO-Brien, 1983, H7 strains associated with haemorrhagic colitits in the United States procedure a Shigella dysenteriae 1 (Shiga) like cytotoxin, Lancet, 1, 702, 10.1016\u002FS0140-6736(83)91987-6\nØrskov, 1984, Serotyping of Escherichia coli, Volume 14, 97\nØrskov, 1985, Escherichia coli in extraintestinal infections, J. Hyg., 95, 551, 10.1017\u002FS0022172400060678\nSack, 1978, The epidemiology of diarrhea due to enterotoxigenic Escherichia coli, J. Infect. Dis., 137, 639, 10.1093\u002Finfdis\u002F137.5.639\nScotland, 1980, Production of cytotoxin affecting Vero cells by strains of Escherichia coli belonging to traditional enteropathogenic serogroups, FEMS Microbiol. Lett., 7, 15, 10.1111\u002Fj.1574-6941.1980.tb01567.x\nSmith, 1985, The toxic role of alpha-haemolysin in the pathogenesis of experimental Escherichia coli infection in mice, J. Gen. Microbiol., 131, 395\nSussman, M.: Escherichia coli in human and animal disease. In: The virulence of Escherichia coli (M. Sussman, ed.), pp. 7–45\nVäisänen, 1981, Mannose-resistant haemagglutination and P antigen recognition are characteristic of Escherichia coli causing primary pyelonephritis, Lancet, 2, 1366, 10.1016\u002FS0140-6736(81)92796-3\nVan den Bosch, 1981, Virulence of Escherichia coli strains from faces of healthy women, Antonie v. Leeuvenhoek, 47, 97, 10.1007\u002FBF02342193\nVan den Bosch, 1982, Virulence of haemolytic strains of Escherichia coli in various animal models, FEMS Microbiol. Lett., 13, 427\nVan den Bosch, 1982, Virulence of urinary and faecal Escherichia coli in relation to serotype, haemolysis and haemagglutination, J. Hyg., 88, 567, 10.1017\u002FS002217240007042X\nWong, 1981, Escherichia coli isolated from urinary tract infections in Hong Kong, 1969 to 1976, Zbl. Bakt. Hyg. 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USA, 75, 1428, 10.1073\u002Fpnas.75.3.1428\nHooper, 1984, Elimination of plasmid pMG110 from Escherichia coli by novobiocin and other inhibitors of DNA gyrase, Antimicrob. Agents Chemother., 25, 586, 10.1128\u002FAAC.25.5.586\nHorinouchi, 1982, Nucleotide sequence and functional map of pE194, a plasmid that specifies inducible resistance to macrolide, lincosamide and streptogramin type B antibiotics, J. Bact., 150, 804, 10.1128\u002FJB.150.2.804-814.1982\nIordanescu, 1976, Three distant plasmids originating in the same Staphylococcus aureus strain, Arch. Roum. Path. Exp. Microbiol., 35, 111\nMazza, 1983, Genetic studies on the transfer of antibiotic resistance genes in Bacillus subtilis strains, Chemioterapia, 2, 64\nMcHugh, 1977, Elimination of plasmids from several bacterial species by novobiocin, Antimicrob. 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Microbiol., 6, 155, 10.1007\u002FBF01642390\nHolländer, 1982, Campylobacter jejuni, ein neuer Enteritis-Erreger, MTA-J., 4, 225\nHolländer, 1975, Characterization of hemophilic and related bacteria by their respiratory quinones and cytochromes, Int. J. system. Bact., 25, 102, 10.1099\u002F00207713-25-2-102\nHolländer, 1977, Lipoquinones of some bacteria and mycoplasmas, with considerations on their functional significance, Antonie v, Leeuwenhoek, 43, 177, 10.1007\u002FBF00395672\nHwang, 1975, Rapid hippurate hydrolysis method for presumptive identification of group B streptococci, J. clin. Microbiol., 1, 114, 10.1128\u002FJCM.1.1.114-115.1975\nLauwers, 1981, Serotyping of Campylobacter jejuni: a useful tool in the epidemiology of campylobacter diarrhoea, 96\nLeaper, 1982, Differentiation between Campylobacter jejuni and allied thermophilic Campylobacters by hybridization of deoxyribonucleic acids, FEMS Microbiol. Lett., 15, 203, 10.1111\u002Fj.1574-6968.1982.tb00068.x\nLior, 1982, Serotyping of Campylobarter jejuni by slide agglutination based on heat-labile antigenic factors, J, clin. Microbiol., 15, 761, 10.1128\u002FJCM.15.5.761-768.1982\nMannheim, 1980, Zur Systematik von Actinobacillus, Haemophilus und Pasteurella: Basenzusammensetzung der DNS, Atmungschinone und kulturellbiochemische Eigenschaften repräsentativer Sammlungsstämme, Zbl. Bakt. Hyg., I. Abt. Orig. A, 246, 512\nPenner, 1980, Passive hemagglutination technique for serotyping Campylobacter fetus ssp. jejuni on the bais of soluble heat stable antigens, J. clin. Microbiol., 12, 732, 10.1128\u002FJCM.12.6.732-737.1980\nSkirrow, 1980, ‘1001’ Campylobacters: cultural characteristics of intestinal Campylobacters from man and animals, J. Hyg. (Camb.), 85, 427, 10.1017\u002FS0022172400063506\nSkirrow, 1981, The classification of ‘thermophilic’ Campylobacters and their distribution in man and domestic animals, 40\nvan Palenstein-Heldermann, 1976, Hydrogen-dependent organisms from the human gingival crevice resembling Vibrio succinogenes, Antonie v. Leeuwenhoek, 42, 107, 10.1007\u002FBF00399454\nVerón, 1973, Taxonomic study of the genus Campylobacter Sebald & Verön and designation of the neotype strain for the type species, Campylobacter fetus (Smith & Taylor) Sebald & Verón, Int. system. Bact., 23, 122, 10.1099\u002F00207713-23-2-122\nVerón, 1981, Anaerobic respiration of fumarate as a differential test between Campylobacter fetus and Campylobacter jejuni, Curr. Microbiol., 6, 349, 10.1007\u002FBF01567010\nWeaver, 1981, Biotype characteristics of Campylobacter species with emphasis on strains isolated in North America, 50\n1981, Gastroenteritis surveillance, Wkly. Epidem. 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Dis., 135, 308, 10.1093\u002Finfdis\u002F135.2.308\nBaker, 1973, Transmission of group B streptococci among parturient women and their neonates, J. Pediat., 83, 919, 10.1016\u002FS0022-3476(73)80524-4\nBaker, 1977, Vaginal colonization with group B streptococcus: A study in college women, J. infect. Dis., 135, 392, 10.1093\u002Finfdis\u002F135.3.392\nBaker, 1977, Immunological investigation of infants with septicemia and meningitis due to group B streptococci, J. infect. Dis., 136, S98, 10.1093\u002Finfdis\u002F136.Supplement.S98\nButtler, 1967, Streptococcus agalactiae as a cause of meningitis in the newborn, and of bacteraemia in adults, Antonie v. Leeuwenhoek, 33, 439, 10.1007\u002FBF02045596\nChretien, 1979, Group B Beta-hemolytic streptococci causing pharyngitis, J. Clin. Microbiol., 10, 263, 10.1128\u002FJCM.10.3.263-266.1979\nChristie, 1944, A note on a lytic phenomenon shown by group B streptococci, Aust. J. exp. Biol. Med. 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(Camb.), 85, 153, 10.1017\u002FS0022172400027169\nWilkinson, 1971, Type-specific antigens of group B type Ic streptococci, Infect. 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Biol., 113, 237, 10.1016\u002F0022-2836(77)90052-3\nRothbaum, 1982, A clinicopathic study of enterocyte-adherent Escherichia coli: A cause of protracted diarrhea in infants, Gastroenterology, 83, 441, 10.1016\u002FS0016-5085(82)80342-9\nScotland, 1980, Production of a cytotoxin affecting Vero cells by strains of Escherichia coli belonging to traditional enteropathogenic serogroups, FEMS Microbiol. Lett., 7, 15, 10.1111\u002Fj.1574-6941.1980.tb01567.x\nSmith, 1971, Observations on the pathogenic properties of the K88, Hly and Ent plasmids of Escherichia coli with particular reference to porcine diarrhoea, J. Med. Microbiol., 4, 476, 10.1099\u002F00222615-4-4-467\nSouthern, 1975, Detection of specific sequences among DNA fragments separated by gel electrophoresis, J. Molec. Biol., 98, 503, 10.1016\u002FS0022-2836(75)80083-0\nSpringer, 1980, Synthesis and secretion of hemolysin by Escherichia coli, J. Bact., 144, 53, 10.1128\u002FJB.144.1.53-59.1980\nVan den Bosch, 1982, Virulence of haemolytic strains of Escherichia coli in various animal models, FEMS Microbiol. Lett., 13, 427\nWagner, 1983, Transport of hemolysin across the outer membrane of Escherichia coli requires two functions, J. Bact., 154, 200, 10.1128\u002FJB.154.1.200-210.1983\nWelch, 1981, Haemolysin contributes to virulence of extra-intestinal E. coli infections, Nature (Lond.), 294, 665, 10.1038\u002F294665a0\nWelch, 1983, Molecular cloning and physical characterization of a chromosomal hemolysin from Escherichia coli, Infect. Immun., 42, 178, 10.1128\u002FIAI.42.1.178-186.1983\nWelch, 1984, Characterization of Escherichia coli hemolysins conferring quantitative differences in virulence, Infect. 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J. Biochem., 107, 485, 10.1111\u002Fj.1432-1033.1980.tb06054.x\nBrenner, 1982, Escherichia vulneris: a new species of Enterobacteriaceae associated with human wounds, J. Clin. Microbiol., 15, 1133, 10.1128\u002FJCM.15.6.1133-1140.1982\nCowan, 1974\nCrosa, 1974, Polynucleotide sequence divergence in the genus Citrobacter, J. gen. Microbiol., 83, 271, 10.1099\u002F00221287-83-2-271\nFarmer, 1980, a new species of “Enterohacteriaceae” isolated from clinical specimens, Int. J. system. Bact., 30, 569, 10.1099\u002F00207713-30-3-569\nFarmer, 1985, Biochemical identification of new species and biogroups of Enterobacteriaceae isolated from clinical specimens, J. Clin. Microbiol., 21, 46, 10.1128\u002FJCM.21.1.46-76.1985\nGavini, 1976, Positions taxonomiques d’enterobactéries H2S — par rapport au genre Citrobacter, Ann. Microbiol. (Inst. Pasteur), 127A, 275\nGavini, 1979, Serratia fonticola, a new species from water, Int. J. system. Bact., 29, 92, 10.1099\u002F00207713-29-2-92\nHickman-Brenner, 1983, Providencia rustigianii: a new species in the family Enterobacteriaceae formerly known as Providencia alcalifaciens biogroup 3, J. Clin. Microbiol., 17, 1057, 10.1128\u002FJCM.17.6.1057-1060.1983\n1984, Vol 1\nLeclerc, 1965, Les Citrobacter, Ann. Inst. Pasteur (Lille), 16, 67\n1980\nMüller, 1983, Providencia friedericiana, a new species isolated from penguins, Int. J. system. Bact., 33, 709, 10.1099\u002F00207713-33-4-709\n.Müller, H. C. M. O’Hara, G. R. Fanning, F. W. Hickman-Brenner, J. M. Swenson, and D. J. Brenner: Providencia heimbacbae, a new species of Enterobacteriaceae, isolated from animals. Int. J. system. Bact., in press\nSteigerwalt, 1976, DNA relatedness among species of Enterobacter and Serratia, Canad. J. Microbiol., 22, 121, 10.1139\u002Fm76-018\nThanbichler, 1974, Catabolism of hamamelose. The anaerobic dissimilation of D-hamamelose by Kluyvera citrophila 627, Europ. J. Biochem., 50, 191, 10.1111\u002Fj.1432-1033.1974.tb03887.x\nThurner, 1978, Numerisch taxonomische Untersuchungen an Enterobakterien aus Oberflächenwasser, Zbl. Bakt. Hyg., I. Abt. Orig., B167, 262",{"EN":1475},"Isolation of serratia fonticola from birds",{"VOID":1477},"10.1016\u002Fs0176-6724(86)80038-4","Author affiliation is blank","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0176672486800384",[1481,1488,1495],{"id":1482,"sortIndex":36,"researcher":26,"roles":1483,"affiliations":1484,"properties":1485},"2df644a4-5837-46d7-a963-bcc2103fb9e4",[704],[],{"title":1486},{"VI":1487},"Hans E. Müller",{"id":1489,"sortIndex":114,"researcher":26,"roles":1490,"affiliations":1491,"properties":1492},"35e67c81-8798-4be8-8f26-9667a638dc30",[704],[],{"title":1493},{"VI":1494},"Don J. 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Dis., 5, 670, 10.1093\u002Fclinids\u002F5.Supplement_4.S670\nBergholm, 1984, The influence of penicillin on growth and morphology of Streptococcus pyogenes in vivo, Zbl. Bakt. Hyg. A, 259, 90\nBisno, 1979, Alternate complement pathway activation by group A streptococci: Role of M protein, Infect. Immun., 26, 1172, 10.1128\u002FIAI.26.3.1172-1176.1979\nBoyüm, 1968, Separation of leucocytes from blood and bone marrow, Scand. J. Clin. Lab. Invest. 21, Suppl., 97, 77\nBribeimm, 1984, Intra- and extracellular events in luminol dependent chemiluminescence of polymorphonuclear leukocytes, Infect. Immun., 45, 1, 10.1128\u002FIAI.45.1.1-5.1984\nCleat, 1984, The mode of action of antibody in neutrophil bactericidal activity against highly pathogenic group-B streptococci, Med. Microbiol. Immunol., 173, 65, 10.1007\u002FBF02124820\nEschenbach, 1982, Luminol-chemilumineszenz phagocytierender neutrophiler Granulozyten, Klin. Wschr., 60, 357, 10.1007\u002FBF01721626\nGambal, 1971, Simple, rapid procedure for isolating serum albumin, Biochim. Biophys. Acta, 251, 54, 10.1016\u002F0005-2795(71)90058-4\nGambill, 1973, Mechanism of immunity in typhus infections, III. Influence of human immune serum on the fate of Rickettsia mooseri within human macrophages. Infect. Immun., 8, 631\nGemmell, 1981, Phagocytosis and killing of Streptococcus pyogenes by human alveolar macrophages, Infect. Immun., 32, 1298, 10.1128\u002FIAI.32.3.1298-1300.1981\nGemmell, 1981, Potentiation of opsonization and phagocytosis of Streptococcus pyogenes following growth in presence of Clindamycin, J. Clin. Invest., 67, 1249, 10.1172\u002FJCI110152\nHolt, 1984, Albumin inhibits human polymorphonuclear leucocyte luminol-dependent chemiluminescence: evidence for oxygen radical scavenning, Brit. J. exp. Path., 65, 231\nIwata, 1978, Electron microscopic study on phagocytosis of staphylococci by mouse peritoneal macrophages, Infect. Immun., 19, 649, 10.1128\u002FIAI.19.2.649-658.1978\nJacks-Weis, 1982, Restricted deposition of C3 on M+ group A streptococci: Correlation with resistance to phagocytosis, J. Immunol., 128, 1897, 10.4049\u002Fjimmunol.128.4.1897\nLancefield, 1957, Differentiation of group A streptococci with a common R antigen into three serological types with special reference to the bactericidal test, J. exp. Med., 106, 525, 10.1084\u002Fjem.106.4.525\nLancefield, 1959, Persistence of type-specific antibodies in man following infection with group A streptococci, J. exp. Med., 110, 271, 10.1084\u002Fjem.110.2.271\nLeijh, 1980, Effect of extracellular serum in the stimulation of intracellular killing of streptococci by human monocytes, Infect. Immun., 30, 421, 10.1128\u002Fiai.30.2.421-426.1980\nLeijh, 1982, Membrane stimulation and intracellular killing by monocytes, Immunobiol., 161, 345, 10.1016\u002FS0171-2985(82)80091-0\nMyrhe, 1980, Demonstration of specific binding sites for human serum albumin in group C and G-streptococci, Infect. Immun., 27, 6, 10.1128\u002FIAI.27.1.6-14.1980\nRobinson, 1984, Chemiluminescence response to pathogenic organisms: normal human polymorphonuclear leukocytes, Infect. Immun., 43, 744, 10.1128\u002FIAI.43.2.744-752.1984\nSanford, 1982, Fibrinogen-mediated adherence of group A streptococcus to influenza A virus-infected cell cultures, Infect. Immun., 38, 513, 10.1128\u002FIAI.38.2.513-520.1982\nSimpson, 1980, Fatty acid binding sites of serum albumin as membrane receptor analogs for streptococcal lipoteichoic acid, Infect. Immun., 29, 119, 10.1128\u002FIAI.29.1.119-122.1980\nSimpson, 1982, Fibronectin-mediated binding of group A streptococci to human polymorphonuclear leucocytes, Infect. Immun., 37, 805, 10.1128\u002FIAI.37.2.805-810.1982\nSimpson, 1983, Adherence of group A streptococci to fibronectin on, oral epithelial cells, Infect. Immun., 39, 275, 10.1128\u002FIAI.39.1.275-279.1983\nSpeert, 1981, Enhanced phagocytosis of group A streptococci M type 6 by oleic acid, J. infect. Dis., 143, 570, 10.1093\u002Finfdis\u002F143.4.570\nSpeziale, 1984, Fibronectin binding to a Streptococcus pyogenes strain, J. Bact., 157, 420, 10.1128\u002FJB.157.2.420-427.1984\nStollerman, 1958, Accessory plasma factors involved in the bactericidal test for type-specific antibody to group A streptococci, I. A typical behaviour of some human and rabbit bloods. J. exp. Med., 108, 475\nVan Furth, 1973, In vitro determination of phagocytosis and intracellular killing by polymorphonuclear and mononuclear phagocytes, 36.1\nWan Oss, 1978, Phagocytosis as a surface phenomenon, Amer. Rev. Microbiol., 32, 19, 10.1146\u002Fannurev.mi.32.100178.000315\nWhitnack, 1982, Antiopsonic activity of fibrinogen bound to M protein on the surface of group A streptococci, J. Clin. Invest., 69, 1042, 10.1172\u002FJCI110508\nWhitnack, 1984, Common protective antigens of group A streptococcal M-proteins masked by fibrinogen, J. exp. Med., 159, 1201, 10.1084\u002Fjem.159.4.1201\nWidehäck, 1983, Demonstration of a receptor for mouse and human serum albumin in Streptococcus pyogenes, Acta path, microbiol. scand. Sect. 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