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Dau-Ming Niu

Showing results (161-170 of 184) with videos related to

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Circulation. Cardiovascular Genetics|December 25, 2009
High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese populationHsiang-Yu Lin, Kah-Wai Chong, Ju-Hui Hsu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Jui-Lung Yen, et al.
Journal of Personalized Medicine|November 27, 2021
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann SyndromeHsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, et al.
Annals of Human Genetics|October 21, 2009
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndromeChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Journal of Medical Internet Research|January 30, 2026
Assessing the Evolution and Influence of Medical Open Databases on Biomedical Research and Health Care Innovation: A 25-Year Perspective With a Focus on Privacy and Privacy-Enhancing TechnologiesAlbert Yang, Mei-Lien Pan, Henry Horng-Shing Lu, 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.
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.
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.
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.
Pageof 19

Showing results (161-170 of 184) with videos related to

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Pageof 19
Circulation. Cardiovascular Genetics|December 25, 2009
High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese populationHsiang-Yu Lin, Kah-Wai Chong, Ju-Hui Hsu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Jui-Lung Yen, et al.
Journal of Personalized Medicine|November 27, 2021
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann SyndromeHsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, et al.
Annals of Human Genetics|October 21, 2009
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndromeChia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, et al.
Journal of Medical Internet Research|January 30, 2026
Assessing the Evolution and Influence of Medical Open Databases on Biomedical Research and Health Care Innovation: A 25-Year Perspective With a Focus on Privacy and Privacy-Enhancing TechnologiesAlbert Yang, Mei-Lien Pan, Henry Horng-Shing Lu, 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.
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.
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.
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.
Pageof 19