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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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Trends in morbidity and mortality among very-low-birth-weight infants from 2003 to 2008 in Japan, Pediatr Res., 72, 531, 10.1038\u002Fpr.2012.114\nSu, 2015, Premature Baby Foundation of Taiwan (PBFT). Neonatal outcomes of extremely preterm infants from Taiwan: comparison with Canada, Japan, and the USA. Pediatr Neonatol., 56, 46, 10.1016\u002Fj.pedneo.2014.05.002\nMoore, 2012, Neurological and developmental outcome in extremely preterm children born in England in 1995 and 2006: The EPICure studies, BMJ., 345, e7961, 10.1136\u002Fbmj.e7961\nIriondo, 2011, Grupo de reanimación neonatal de la Sociedad Española de Neonatología. Adaptación de las recomendaciones internacionales sobre reanimación neonatal 2010: comentarios [Changes in the international recommendations on neonatal resuscitation 2010 comments], An Pediatr (Barc), 75, 203\nMarlow, 2005, EPICure Study Group. Neurologic and developmental disability at six years of age after extremely preterm birth, N Engl J Med., 352, 9, 10.1056\u002FNEJMoa041367\nAmerican College of Obstetricians and Gynecologists and the Society for Maternal–Fetal Medicine, Ecker JL, Kaimal A, Mercer BM, Blackwell SC, deRegnier RA, Farrell RM, et al. Periviable birth: interim update. Am J Obstet Gynecol. 2016; 215(2):B2-B12.e1. doi: 10.1016\u002Fj.ajog.2016.04.017.\nLawrence, 2021, Ethical Cultures in Perinatal Care: Do They Exist? 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Results from a European cooperative study, J Clin Endocrinol Metab, 85, 286\nClaes, 2011, The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP), Acta Gastroenterol Belg., 74, 421\nRichards, 2010, Familial syndromes associated with thyroid cancer in the era of personalized medicine, Thyroid., 20, 707, 10.1089\u002Fthy.2010.1641\nCao, 2016, Clinicopathological features and prognosis of fPTC-a large scale, matched, case-control study, Clin. Endo- crinol., 84, 598, 10.1111\u002Fcen.12859\nGara, 2015, Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer, N Engl J Med, 373, 448, 10.1056\u002FNEJMoa1502449\nVriens, 2009, Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer, Thyroid, 19, 1343, 10.1089\u002Fthy.2009.1607\nCantara, 2012, Telomere Abnormalities and Chromosome Fragility in Patients Affected by Familial Papillary Thyroid Cancer, J Clin Endocrinol Metab, 97, E1327, 10.1210\u002Fjc.2011-2096\nCantara, 2017, HABP2 G534E variation in familial non-medullary thyroid cancer: an Italian series J Endocrinol Invest., 40, 557\nHABP2 Mutation and Nonmedullary Thyroid Cancer. 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Trastornos psiquiátricos enniños y adolescentes chilenos:un estudio de prevalencia comunitario. Tráabajo en vías de publicación.\nCorrea, 2006, Prevalencia de riesgo de trastornos alimentarios en adolescentes mujeres escolares de la Región Metropolitana, Revista Chilena de Pediatría, 77, 153, 10.4067\u002FS0370-41062006000200005\nBehar, 2007, Detección de actitudes y\u002Fo conductas predisponentes a trastornos alimentarios en estudiantes de enseñanza media de tres colegios particulares de Viña del Mar, Rev Chil Nutr., 34, 240, 10.4067\u002FS0717-75182007000300008\nUrzúa, 2011, Prevalencia de riesgo de trastornos alimentarios en adolescentes escolarizados del norte de Chile, Rev Chil Nutr., 38, 128, 10.4067\u002FS0717-75182011000200003\n2000\n1992\nLe Grange, 2011\nLe Grange, 2007, Early identification and treatment of eating disorders: Prodrome to syndrome, Early Intervention in Psychiatry, 27, 10.1111\u002Fj.1751-7893.2007.00007.x\nBirgegard, 2012, DSM-IV Versus DSM-5: Implementation of Proposed DSM-5 Criteria in a Large Naturalistic Database, International Journal of Eating Disorders, 45, 353, 10.1002\u002Feat.20968\nWonderlich, 2009, The validity and clinical utility of binge eating disorder, International Journal of Eating Disorders, 42, 487, 10.1002\u002Feat.20719\n2012\nKeel, 2011, Clinical significance and distinctiveness of purging disorder and binge eating disorder, International Journal of Eating Disorders, 44, 311, 10.1002\u002Feat.20821\nStriegel-Moore, 2009, The validity and clinical utility of night eating syndrome, International Journal of Eating Disorders, 42, 720, 10.1002\u002Feat.20721\nFairburn, 2011, Eating Disorders, DSM-5 and clinical reality, British Journal of Psychiatry, 198, 8, 10.1192\u002Fbjp.bp.110.083881\nGaete, 2011, Atención clínica del adolescente que consulta por un problema de salud, Rev Med Clin Condes, 22, 5\nHerpertz-Dahlmann, 2008, Adolescent eating disorders: definitions, symptomatology, epidemiology, and comorbidity, Child Adolesc Psychiatric Clin N Am., 18, 31, 10.1016\u002Fj.chc.2008.07.005\nMiller, 2002",{"ES":2546},"Trastornos de la conducta alimentaria en adolescentes y jóvenes",{"VOID":2548},"10.1016\u002Fs0716-8640(12)70351-6","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0716864012703516",[2551,2568,2590],{"id":2552,"sortIndex":114,"researcher":26,"roles":2553,"affiliations":2554,"properties":2565},"1ca9e89e-eded-4f9e-991e-456dfa3a482f",[750],[2555],{"id":26,"sortIndex":36,"affiliation":2556,"properties":26},{"id":2557,"createTime":2558,"updateTime":2559,"relativeEntities":2560,"slug":2561,"properties":2562,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"040a7cb6-7167-479b-928f-0f94bdb8d9a4","2024-01-30T06:26:13.143+00:00","2025-06-11T17:20:16.210+00:00",[],"Centro-de-Adolescentes-y-J%C3%B3venes-Departamento-de-Pediatr%C3%ADa-Cl%C3%ADnica-Las-Condes-y-Centro-de-Salud-del-Adolescente-Serjoven-dEpartamento-de-PEdiatr%C3%ADa-y-Cirug%C3%ADa-Infantil-Oriente-Facultad-de-Medicina-Universidad-de-Chile-",{"title":2563},{"VI":2564},"Centro de Adolescentes y Jóvenes, Departamento de Pediatría. 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Report of fifteen cases, Paediatr Univ Tokyo (Tokyo), 4, 5\nSantavuori, 1977, Muscle, eye and brain disease: a new syndrome, Neuropädiatrie, 8, 553, 10.1055\u002Fs-0028-1091594\nBatten, 1910, Critical review: The myopathies or muscular dystrophies, Quart J Med, 3, 313, 10.1136\u002Fbmj.3.5613.313\nDubowitz V. 22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May (1993). Neuromuscul Disord, 1994. 4.(75-81).\nFerreiro, 2002, Mutations of the selenoprotein N gene, which is implicated in Rigid Spine Muscular Dystrophy, cause the Classical phenotype of Multiminicore Disease: reassessing the nosology of early-onset myopathies, Am J Hum Genet, 1, 739, 10.1086\u002F342719\nBrockington, 2001, Mutations in the fukutin-related protein gene (FKRP) identifies limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C, Hum Mol Genet, 10, 2851, 10.1093\u002Fhmg\u002F10.25.2851\nBonne, 1999, Mutations in the gene encoding lamin A\u002FC cause autosomal dominant Emery-Dreifuss muscular dystrophy, Nat Genet., 21, 285, 10.1038\u002F6799\nAllamand, 2011, ColVI myopathies: where do we stand, where do we go?, Skelet Muscle., 1, 30, 10.1186\u002F2044-5040-1-30\nSparks SE, Quijano-Roy S, Harper A, Rutkowski A, Gordon E, Hoffman EP, et al. Congenital Muscular Dystrophy Overview. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.2001 Jan 22.[updated 2012 Aug 23].\nDubowitz, 1973, Rigid spine syndrome: a muscle syndrome in search of a name, Proc Roy Soc Med, 66, 219, 10.1177\u002F003591577306600304\nMoghadaszadeh, 2001, Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome, Nat Genet., 29, 17, 10.1038\u002Fng713\nTomé, 1994, Congenital muscular dystrophy with merosin deficiency, C R Acad Sci III., 317, 351\nClement, 2012, Relative frequency of congenital muscular dystrophy subtypes: analysis of the UK diagnostic service 2001-2008, Neuromuscul Disord., 22, 522, 10.1016\u002Fj.nmd.2012.01.010\nHelbling-Leclerc, 1995, Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2, C R Acad Sci III., 318, 1245\nFardeau, 1996, Dystrophie musculaire congénitale avec déficience en mérosine: analyse clinique, histopathologique, immuno-cytochimique et génétique, Rev Neurol (Paris), 152, 11\nHayashi, 1997, A benign allelic form of laminin-a2 chain deficient muscular dystrophy, Lancet, 349, 1147, 10.1016\u002FS0140-6736(05)63023-1\nQuijano-Roy, 2002, Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency, Neuromuscul Disord., 12, 466, 10.1016\u002FS0960-8966(01)00331-5\nLamer, 1998, Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency, Radiology., 206, 811, 10.1148\u002Fradiology.206.3.9494506\nSijens, 2007, MR spectroscopy and diffusion tensor imaging of the brain in congenital muscular dystrophy with merosin deficiency: metabolite level decreases, fractional anisotropy decreases, and apparent diffusion coefficient increases in the white matter, Brain Dev., 29, 317, 10.1016\u002Fj.braindev.2006.10.004\nQuijano-Roy, 2004, EMG and nerve conduction studies in children with congenital muscular dystrophy, Muscle Nerve., 29, 292, 10.1002\u002Fmus.10544\nGeranmayeh, 2010, Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations, Neuromuscul Disord., 20, 241, 10.1016\u002Fj.nmd.2010.02.001\nMorillon, 2007, [Effect of thoracic bracing on lung function in children with neuromuscular disease].[Article in French], Ann Readapt Med Phys., 50, 645, 10.1016\u002Fj.annrmp.2007.03.018\nOdent, 2015, Fusionless surgery in early-onset scoliosis, Orthop Traumatol Surg Res., 101, S281, 10.1016\u002Fj.otsr.2015.07.004\nMiladi L, Gaume M, Khouri N, Johnson M, Topouchian V, Glorion C. Minimally Invasive Surgery for Neuromuscular Scoliosis: Results and Complications in a Series of one hundred Patients. Spine (Phila Pa 1976). 2018 Feb 6. D.\nUllrich, 1930, Kongenitale, atonisch-sclerotische muskeldystrophie, Monatsschr Kinderheikd,, 68, 502\nCamacho Vanegas, 2001, Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen VI, Proc Natl Acad Sci, 98, 7516, 10.1073\u002Fpnas.121027598\nBriñas, 2010, Early onset collagen VI myopathies: Genetic and clinical correlations, Ann Neurol., 68, 511, 10.1002\u002Fana.22087\nFoley, 2013, Natural history of pulmonary function in collagen VI-related myopathies, Brain., 136, 3625, 10.1093\u002Fbrain\u002Fawt284\nQuijano-Roy, 2014, Diaphragmatic dysfunction in Collagen VI myopathies, Neuromuscul Disord., 24, 125, 10.1016\u002Fj.nmd.2013.11.002\nQuijano-Roy, 2012, Whole body muscle MRI protocol: pattern recognition in early onset NM disorders, Neuromuscul Disord., 22, S68, 10.1016\u002Fj.nmd.2012.08.003\nTordjman M, Dabaj I, Laforet P, Felter A, Ferreiro A, Biyoukar M, et al. Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity. Eur Radiol. 2018 May 25.\nMercuri, 2005, Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy, Neuromuscul Disord., 15, 303, 10.1016\u002Fj.nmd.2005.01.004\nMercuri, 2010, Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine, Ann Neurol., 67, 201, 10.1002\u002Fana.21846\nScoto, 2011, SEPN1-related myopathies: clinical course in a large cohort of patients, Neurology., 76, 2073, 10.1212\u002FWNL.0b013e31821f467c\nCaggiano, 2017, Diaphragmatic dysfunction in SEPN1-related myopathy, Neuromuscul Disord., 27, 747, 10.1016\u002Fj.nmd.2017.04.010\nHankiewicz, 2015, Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable pattern, Muscle Nerve., 52, 728, 10.1002\u002Fmus.24634\nGómez-Andrés, 2016, Pediatric laminopathies: Whole-body magnetic resonance imaging fingerprint and comparison with Sepn1 myopathy, Muscle Nerve., 54, 192, 10.1002\u002Fmus.25018\nCarlier, 2015, Skeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patients, J Inherit Metab Dis., 38, 565, 10.1007\u002Fs10545-015-9825-9\nQuijano-Roy, 2008, De novo LMNA mutations cause a new form of congenital muscular dystrophy, Ann Neurol., 64, 177, 10.1002\u002Fana.21417\nBonne, 2013, Emery-Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies, Handb Clin Neurol., 113, 1367, 10.1016\u002FB978-0-444-59565-2.00007-1\nHeller, 2017, Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care, Cardiol Young., 27, 1076, 10.1017\u002FS1047951116002079\nGodfrey, 2007, Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan, Brain., 130, 2725, 10.1093\u002Fbrain\u002Fawm212\nQuijano-Roy, 2006, Brain MRI abnormalities in muscular dystrophy due to FKRP mutations, Brain Dev., 28, 232, 10.1016\u002Fj.braindev.2005.08.003\nClement, 2008, Brain involvement in muscular dystrophies with defective dystroglycan glycosylation, Ann Neurol., 64, 573, 10.1002\u002Fana.21482\nGodfrey, 2011, Dystroglycanopathies: coming into focus, Curr Opin Genet Dev., 21, 278, 10.1016\u002Fj.gde.2011.02.001\nBouchet-Séraphin, 2015, Dystroglycanopathies: About Numerous Genes Involved in Glycosylation of One Single Glycoprotein, J Neuromuscul Dis., 2, 27, 10.3233\u002FJND-140047\nKanagawa, 2017, Muscular Dystrophy with Ribitol-Phosphate Deficiency: A Novel Post-Translational Mechanism in Dystroglycanopathy, J Neuromuscul Dis., 4, 259, 10.3233\u002FJND-170255\nGerin, 2016, ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto (-dystroglycan, Nat Commun., 7, 11534, 10.1038\u002Fncomms11534\nPane, 2012, Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency, Neuromuscul Disord., 22, 685, 10.1016\u002Fj.nmd.2012.05.006",{"ES":2651},"Distrofias musculares congénitas",{"VOID":2653},"10.1016\u002Fj.rmclc.2018.08.002","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0716864018301007",[2656,2671],{"id":2657,"sortIndex":36,"researcher":26,"roles":2658,"affiliations":2659,"properties":2668},"281c8d77-f588-4b02-9795-ce59cf886f4d",[750],[2660],{"id":26,"sortIndex":36,"affiliation":2661,"properties":26},{"id":2662,"createTime":2663,"updateTime":2663,"relativeEntities":2664,"slug":26,"properties":2665,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"7d81da1f-b82b-4a33-9719-c8cacad6fb82","2023-12-04T04:53:25.917+00:00",[],{"title":2666},{"VI":2667},"AP-HP, Unidad Neuromuscular, Servicio de Neurología, Cuidados Intensivos y Rehabilitación Pediatras, Hospital Universitario Raymond Poincaré, HU Paris- Ile-de-France Ouest, Garches; U1179 INSERM, Université Versailles (UVSQ) Francia",{"title":2669},{"VI":2670},"Susana Quijano-Roy",{"id":2672,"sortIndex":115,"researcher":26,"roles":2673,"affiliations":2674,"properties":2683},"11f2b9b9-0dcd-4eef-a3f1-16687d5fd49d",[750],[2675],{"id":26,"sortIndex":36,"affiliation":2676,"properties":26},{"id":2677,"createTime":2678,"updateTime":2678,"relativeEntities":2679,"slug":26,"properties":2680,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"cdbf57aa-35bd-4c86-9052-26ef317de257","2023-12-04T04:53:25.925+00:00",[],{"title":2681},{"VI":2682},"AP-HP, Unidad Neuromuscular, Servicio de Neurología, Cuidados Intensivos y Rehabilitación Pediatras. 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2001, The Sequence of the Human Genome, Science, 291, 1304, 10.1126\u002Fscience.1058040\n2001, Initial sequencing and analysis of the human genome, Nature, 409, 860, 10.1038\u002F35057062\nKoboldt, 2013, The next-generation sequencing revolution and its impact on genomics, Cell, 155, 27, 10.1016\u002Fj.cell.2013.09.006\nMonges, 2017, Management of neuromuscular diseases and spinal muscular atrophy in Latin America, Gene Ther, 9, 578, 10.1038\u002Fgt.2017.68\nEfthymiou, 2016, Next-generation sequencing in neuromuscular diseases, Curr Opin Neurol., 5, 527, 10.1097\u002FWCO.0000000000000374\nDarras B, Urion D and Ghosh, P. Dystrophinopathies. GeneReviews. Update: April 26, 2018.(https:\u002F\u002Fwww.ncbi.nlm.nih.gov\u002Fbooks\u002FNBK1119\u002F).\nSoltanzadeh, 2010, Clinical and genetic characterization of manifesting carriers of DMD mutations, Neuromuscul Disord, 20, 499, 10.1016\u002Fj.nmd.2010.05.010\nChamberlain, 1992, Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study, JAMA, 267, 2609, 10.1001\u002Fjama.1992.03480190051030\nPrior T, Finanger E. Spinal Muscular Atrophy. 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Charcot-Marie-Tooth Hereditary Neuropathy Overview. GeneReviews. Revision: September 1, 2016.(Internet: https:\u002F\u002Fwww.ncbi.nlm.nih.gov\u002Fbooks\u002FNBK1358\u002F).\nFink J. Hereditary Spastic Paraplegia Overview (Synonyms: Familial Spastic Paraplegia, Hereditary Spastic Paraparesis, Strumpell-Lorrain Syndrome). GeneReviews. Update: February 6, 2014.(https:\u002F\u002Fwww.ncbi.nlm.nih.gov\u002Fbooks\u002FNBK1509\u002F).\nParodi, 2017, Hereditary spastic paraplegia: More than an upper motor neuron disease, Rev Neurol (Paris), 173, 352, 10.1016\u002Fj.neurol.2017.03.034\nBird T. Hereditary Ataxia Overview. GeneReviews. 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