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Electrophoresis|February 16, 2007
Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CEChia-Cheng Hung, Yi-Ning Su, Po-Nien Tsao, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Free Radical Research|December 23, 2024
Hyperoxia induces autophagy in pulmonary epithelial cells: insights from in vivo and in vitro experimentsKuo-Tsang Huang, Wen-Hui Tsai, Chih-Wei Chen, et al.
Molecular Genetics and Metabolism Reports|May 3, 2016
Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case seriesHsiang-Yu Lin, Chih-Kuang Chuang, Chung-Hsing Wang, et al.
Molecular Genetics and Metabolism|February 23, 2016
Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VIHsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Journal of Inherited Metabolic Disease|October 7, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in TaiwanHsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|August 3, 2018
Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21-year periodHsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
JIMD Reports|February 23, 2013
Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria PatientsMei-Ying Liu, Tze-Tze Liu, Yang-Ling Yang, et al.
Diagnostics (Basel, Switzerland)|May 14, 2025
Functional Independence of Taiwanese Children with Silver-Russell SyndromeHung-Hsiang Fang, Chung-Lin Lee, Chih-Kuang Chuang, et al.
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.
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