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Plos One|October 7, 2020
Acute kidney injury is a common complication in children and adolescents hospitalized for diabetic ketoacidosisShih-Kang Huang, Chi-Yu Huang, Chao-Hsu Lin, et al.Oncotarget|April 18, 2018
Autoantibodies against islet cell antigens in children with type 1 diabetes mellitusBi-Wen Cheng, Fu-Sung Lo, An-Mei Wang, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|October 27, 2017
Factors associated with diabetic nephropathy in children, adolescents, and adults with type 1 diabetesChi-Yu Huang, Wei-Hsin Ting, Fu-Sung Lo, et al.Pediatrics and Neonatology|January 26, 2020
Long-term outcomes of graves disease in children treated with anti-thyroid drugsYa-Ting Chiang, Wei-Hsin Ting, Chi-Yu Huang, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 23, 2018
Mutations in glucokinase and other genes detected in neonatal and type 1B diabetes patient using whole exome sequencing may lead to disease-causing changes in protein activityDao-Chen Lin, Chi-Yu Huang, Wei-Hsin Ting, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 5, 2022
Effect of Oral Vitamin D3 Supplementation in Exclusively Breastfed Newborns: Prospective, Randomized, Double-Blind, Placebo-Controlled TrialChao-Hsu Lin, Chien-Yu Lin, Yi-Hsiang Sung, et al.Plos One|March 22, 2014
Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic ChineseYi-Lei Wu, Daw-Yang Hwang, Hui-Pin Hsiao, et al.Diagnostics (Basel, Switzerland)|April 13, 2023
Application of Drug Testing Platforms in Circulating Tumor Cells and Validation of a Patient-Derived Xenograft Mouse Model in Patient with Primary Intracranial Ependymomas with Extraneural MetastasesMuh-Lii Liang, Ting-Chi Yeh, Man-Hsu Huang, et al.Plos One|April 26, 2016
Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control StudyWei-Hsin Ting, Ming-Nan Chien, Fu-Sung Lo, et al.In Vivo (Athens, Greece)|December 26, 2023
Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 PatientsPen-Hua Su, Ju-Shan Yu, Yu-Zhen Wu, et al.Pageof 3