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European Journal of Clinical Investigation
|
November 6, 2025
Long-term effectiveness and safety outcomes in adults with Fabry disease treated with agalsidase alfa: 20 years of data from the Fabry Outcome Survey
Derralynn A Hughes, Guillem Pintos-Morell, Christoph Kampmann, et al.
Orphanet Journal of Rare Diseases
|
February 12, 2014
Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA
Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Molecular Genetics & Genomic Medicine
|
October 9, 2018
The relationships between urinary glycosaminoglycan levels and phenotypes of mucopolysaccharidoses
Hsiang-Yu Lin, Chung-Lin Lee, Yun-Ting Lo, et al.
The Canadian Journal of Cardiology
|
March 9, 2025
Early Potentially Irreversible Cardiac Damage in Fabry Disease Precedes Gb3 Inclusion Body Formation
Chung-Lin Lee, Pei-Sin Chen, Yu-Ying Lu, et al.
Pediatric Pulmonology
|
August 19, 2010
Polysomnographic characteristics in patients with mucopolysaccharidoses
Hsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, et al.
Gene Therapy
|
April 18, 2026
Beneficial bystander-enhanced cryptic splice rescue of cardiac-type Fabry GLA IVS4+919G>A by adenine base editing in patient fibroblasts
Hua-Chuan Chao, Yu-Ying Lu, Yu-Ting Chiang, et al.
Molecular Genetics and Metabolism Reports
|
April 25, 2025
Two decades of experience of the Fabry Outcome Survey provides further confirmation of the long-term effectiveness of agalsidase alfa enzyme replacement therapy
Uma Ramaswami, Guillem Pintos-Morell, Christoph Kampmann, et al.
World Journal of Surgery
|
September 16, 2011
Comparison of the survival difference between AJCC 6th and 7th editions for gastric cancer patients
Wen-Liang Fang, Kuo-Hung Huang, Jen-Hao Chen, et al.
Investigative Ophthalmology & Visual Science
|
July 9, 2016
Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa
Nana Hsiang-Hua Wang, Shih-Jen Chen, Chi-Fan Yang, et al.
Journal of Inherited Metabolic Disease
|
June 4, 2010
Clinical observations, molecular genetic analysis, and treatment of sitosterolemia in infants and children
Dau-Ming Niu, Kah-Wai Chong, Ju-Hui Hsu, et al.
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Search research articles
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Showing results (111-120 of 184) with videos related to
Sort By:
Page
of 19
European Journal of Clinical Investigation
|
November 6, 2025
Long-term effectiveness and safety outcomes in adults with Fabry disease treated with agalsidase alfa: 20 years of data from the Fabry Outcome Survey
Derralynn A Hughes, Guillem Pintos-Morell, Christoph Kampmann, et al.
Orphanet Journal of Rare Diseases
|
February 12, 2014
Natural history and clinical assessment of Taiwanese patients with mucopolysaccharidosis IVA
Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Molecular Genetics & Genomic Medicine
|
October 9, 2018
The relationships between urinary glycosaminoglycan levels and phenotypes of mucopolysaccharidoses
Hsiang-Yu Lin, Chung-Lin Lee, Yun-Ting Lo, et al.
The Canadian Journal of Cardiology
|
March 9, 2025
Early Potentially Irreversible Cardiac Damage in Fabry Disease Precedes Gb3 Inclusion Body Formation
Chung-Lin Lee, Pei-Sin Chen, Yu-Ying Lu, et al.
Pediatric Pulmonology
|
August 19, 2010
Polysomnographic characteristics in patients with mucopolysaccharidoses
Hsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, et al.
Gene Therapy
|
April 18, 2026
Beneficial bystander-enhanced cryptic splice rescue of cardiac-type Fabry GLA IVS4+919G>A by adenine base editing in patient fibroblasts
Hua-Chuan Chao, Yu-Ying Lu, Yu-Ting Chiang, et al.
Molecular Genetics and Metabolism Reports
|
April 25, 2025
Two decades of experience of the Fabry Outcome Survey provides further confirmation of the long-term effectiveness of agalsidase alfa enzyme replacement therapy
Uma Ramaswami, Guillem Pintos-Morell, Christoph Kampmann, et al.
World Journal of Surgery
|
September 16, 2011
Comparison of the survival difference between AJCC 6th and 7th editions for gastric cancer patients
Wen-Liang Fang, Kuo-Hung Huang, Jen-Hao Chen, et al.
Investigative Ophthalmology & Visual Science
|
July 9, 2016
Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa
Nana Hsiang-Hua Wang, Shih-Jen Chen, Chi-Fan Yang, et al.
Journal of Inherited Metabolic Disease
|
June 4, 2010
Clinical observations, molecular genetic analysis, and treatment of sitosterolemia in infants and children
Dau-Ming Niu, Kah-Wai Chong, Ju-Hui Hsu, et al.
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of 19