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Medicina (Kaunas, Lithuania)|January 21, 2022
Increased Diagnostic Yield of Array Comparative Genomic Hybridization for Autism Spectrum Disorder in One Institution in TaiwanChung-Lin Lee, Chih-Kuang Chuang, Ru-Yi Tu, et al.
International Journal of Molecular Sciences|September 9, 2022
Updated Confirmatory Diagnosis for Mucopolysaccharidoses in Taiwanese Infants and the Application of Gene VariantsChih-Kuang Chuang, Yuan-Rong Tu, Chung-Lin Lee, 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.
The Journal of Pediatrics|November 10, 2018
Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VIMin-Ju Chan, Hsuan-Chieh Liao, Michael H Gelb, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
Nationwide Newborn Screening Program for Mucopolysaccharidoses in Taiwan and an Update of the "Gold Standard" Criteria Required to Make a Confirmatory DiagnosisChih-Kuang Chuang, Chung-Lin Lee, Ru-Yi Tu, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Functional independence of Taiwanese children with Prader-Willi syndromeChung-Lin Lee, Hsiang-Yu Lin, Li-Ping Tsai, et al.
Orphanet Journal of Rare Diseases|May 27, 2018
Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in TaiwanChih-Kuang Chuang, Hsiang-Yu Lin, Tuan-Jen 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|November 5, 2011
Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndromeDar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, et al.
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