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Orphanet Journal of Rare Diseases
|
May 27, 2018
Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan
Chih-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 VI
Hsiang-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 Taiwan
Hsiang-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 syndrome
Dar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, 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 period
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
Journal of Clinical Immunology
|
February 26, 2008
Lack of association of the vascular endothelial growth factor gene polymorphisms with Kawasaki disease in Taiwanese children
Fu-Yuan Huang, Tzu-Yang Chang, Ming-Ren Chen, et al.
Journal of the Chinese Medical Association : JCMA
|
June 24, 2008
Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndrome
Hsiang-Yu Lin, Shuan-Pei Lin, Li-Ping Tsai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 9, 2026
Nationwide Newborn Screening for Mucopolysaccharidoses in Taiwan: Impact, Early Diagnosis, and Clinical Advances over the Past Decade
Chih-Kuang Chuang, Yuan-Rong Tu, Chung-Lin Lee, et al.
Journal of the Chinese Medical Association : JCMA
|
January 7, 2014
Clinical observations on enzyme replacement therapy in patients with Fabry disease and the switch from agalsidase beta to agalsidase alfa
Hsiang-Yu Lin, Yu-Hsiu Huang, Hsuan-Chieh Liao, et al.
JIMD Reports
|
February 23, 2013
Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients
Mei-Ying Liu, Tze-Tze Liu, Yang-Ling Yang, et al.
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of 29
Search research articles
Search
Showing results (241-250 of 281) with videos related to
Sort By:
Page
of 29
Orphanet Journal of Rare Diseases
|
May 27, 2018
Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan
Chih-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 VI
Hsiang-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 Taiwan
Hsiang-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 syndrome
Dar-Shong Lin, Jui-Hsing Chang, Hsuan-Liang Liu, 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 period
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
Journal of Clinical Immunology
|
February 26, 2008
Lack of association of the vascular endothelial growth factor gene polymorphisms with Kawasaki disease in Taiwanese children
Fu-Yuan Huang, Tzu-Yang Chang, Ming-Ren Chen, et al.
Journal of the Chinese Medical Association : JCMA
|
June 24, 2008
Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndrome
Hsiang-Yu Lin, Shuan-Pei Lin, Li-Ping Tsai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 9, 2026
Nationwide Newborn Screening for Mucopolysaccharidoses in Taiwan: Impact, Early Diagnosis, and Clinical Advances over the Past Decade
Chih-Kuang Chuang, Yuan-Rong Tu, Chung-Lin Lee, et al.
Journal of the Chinese Medical Association : JCMA
|
January 7, 2014
Clinical observations on enzyme replacement therapy in patients with Fabry disease and the switch from agalsidase beta to agalsidase alfa
Hsiang-Yu Lin, Yu-Hsiu Huang, Hsuan-Chieh Liao, et al.
JIMD Reports
|
February 23, 2013
Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients
Mei-Ying Liu, Tze-Tze Liu, Yang-Ling Yang, et al.
Page
of 29