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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 8, 2024
Implementation of newborn screening for mucopolysaccharidosis type IVA and long-term monitoring in TaiwanHsiang-Yu Lin, Chung-Lin Lee, Ya-Hui Chang, et al.
Journal of Ethnopharmacology|March 27, 2019
Leeches attenuate blood hyperviscosity and related metabolic disorders in rats differently than aspirinXuan Wang, Ming Niu, Shan-Na Wu, et al.
International Journal of Cardiology|January 14, 2017
Energy utilization of induced pluripotent stem cell-derived cardiomyocyte in Fabry diseaseShih-Jie Chou, Wen-Chung Yu, Yuh-Lih Chang, et al.
Molecular Genetics & Genomic Medicine|April 9, 2021
The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry diseaseDominique P Germain, Sergey Moiseev, Fernando Suárez-Obando, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
Identification of lysosomal and extralysosomal globotriaosylceramide (Gb3) accumulations before the occurrence of typical pathological changes in the endomyocardial biopsies of Fabry disease patientsMing-Jia Hsu, Fu-Pang Chang, Yung-Hsiu Lu, et al.
Orphanet Journal of Rare Diseases|April 24, 2025
Newborn screening facilitates early theranostics and improved spinal muscular atrophy outcome: five-year real-world evidence from TaiwanChen-Hua Wang, Ting-Rong Hsu, Mei-Ying Liu, et al.
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