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1
المؤلفون: Min-Yi, Tan, Xiang, Jiang, Hui-Fen, Mei, Yu-Yu, Feng, Ting, Xie, Cheng-Fang, Tang, Qian-Yu, Chen, Chun-Hua, Zeng, Yonglan, Huang
المصدر: Journal of Pediatric Endocrinology and Metabolism. 35:1141-1146
مصطلحات موضوعية: China, Incidence, Endocrinology, Diabetes and Metabolism, Infant, Newborn, Infant, Thyrotropin, Thyroxine, Neonatal Screening, Endocrinology, Child, Preschool, Pediatrics, Perinatology and Child Health, Congenital Hypothyroidism, Humans, Infant, Premature, Iodine, Retrospective Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc74ae3763d71146541c598bc6ede1f3
https://doi.org/10.1515/jpem-2022-0107 -
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المؤلفون: Mo-Ling, Wu, Li, Liu, Xiao-Jian, Mao, Min-Zhi, Peng, Hong-Sheng, Liu, Hui-Ying, Sheng, Yan-Na, Cai, Hui-Fen, Mei, Chun, Fan, Yong-Lan, Huang, Xiu-Zhen, Li, Jing, Cheng
المصدر: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 17(8)
مصطلحات موضوعية: Male, Protein Conformation, Molecular Sequence Data, Mutation, Humans, Infant, Pyruvate Dehydrogenase (Lipoamide), Amino Acid Sequence, Pyruvate Dehydrogenase Complex Deficiency Disease
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::3582f7ff649c0565dfa080b93f6aff50
https://pubmed.ncbi.nlm.nih.gov/26287337 -
3
المؤلفون: Cui-Li, Liang, Li, Liu, Hui-Ying, Sheng, Min-Yan, Jiang, Xi, Yin, Hui-Fen, Mei, Jing, Cheng, Wen, Zhang, Li-Ping, Fan
المصدر: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 15(8)
مصطلحات موضوعية: Male, Monosaccharide Transport Proteins, Child, Preschool, Mutation, Humans, Infant, Female, Sequence Analysis, DNA, Glycogen Storage Disease Type I, Antiporters
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::56dc08caa93071ca36ed099280f495be
https://pubmed.ncbi.nlm.nih.gov/23965881 -
4
المؤلفون: Xiu-Zhen, Li, Li, Liu, Hui-Fen, Mei
المصدر: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 9(5)
مصطلحات موضوعية: Diagnosis, Differential, Glycerol, Male, Glycerol Kinase, Humans, Infant, Genetic Diseases, X-Linked, Adrenal Insufficiency
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::4bfb63687e7c4617460dc5bb69b98664
https://pubmed.ncbi.nlm.nih.gov/17937854