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Orphanet Journal of Rare Diseases|June 29, 2016
Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012Hsiang-Yu Lin, Chih-Kuang Chuang, Yu-Hsiu Huang, et al.Orphanet Journal of Rare Diseases|November 8, 2020
Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985-2019)Hsiang-Yu Lin, Chung-Lin Lee, Chia-Ying Chang, et al.Journal of the Chinese Medical Association : JCMA|July 7, 2010
Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in TaiwanKang-Hsiang Cheng, Mei-Ying Liu, Chuan-Hong Kao, et al.Journal of Proteome Research|June 19, 2014
Metabolomic Profiling of Autoimmune Hepatitis: The Diagnostic Utility of Nuclear Magnetic Resonance SpectroscopyJia-Bo Wang, Shi-Biao Pu, Ying Sun, et al.Frontiers in Pharmacology|April 12, 2016
Untargeted Metabolomics Reveals Dose-Response Characteristics for Effect of Rhubarb in a Rat Model of CholestasisCong-En Zhang, Ming Niu, Rui-Yu Li, et al.Orphanet Journal of Rare Diseases|April 4, 2019
Methylmalonic acidemia/propionic acidemia - the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groupsTzu-Hung Chu, Yin-Hsiu Chien, Hsiang-Yu Lin, et al.Orphanet Journal of Rare Diseases|July 2, 2014
Endomyocardial biopsies in patients with left ventricular hypertrophy and a common Chinese later-onset Fabry mutation (IVS4 + 919G > A)Ting-Rong Hsu, Shih-Hsien Sung, Fu-Pang Chang, et al.Journal of Gastroenterology and Hepatology|February 21, 2016
Hepatobiliary and pancreatic: Comparison between Chinese herbal medicine and Western medicine-induced liver injury of 1985 patientsYun Zhu, Ming Niu, Jing Chen, et al.Molecular Genetics & Genomic Medicine|June 20, 2019
Functional independence of Taiwanese patients with mucopolysaccharidosesChung-Lin Lee, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.Journal of the Chinese Medical Association : JCMA|March 18, 2017
Experiences during newborn screening for glutaric aciduria type 1: Diagnosis, treatment, genotype, phenotype, and outcomesFang-Chih Tsai, Han-Jui Lee, An-Guor Wang, et al.Pageof 50