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Shuan-Pei Lin

Showing results (251-260 of 281) with videos related to

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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.
Plos One|March 22, 2014
Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic ChineseYi-Lei Wu, Daw-Yang Hwang, Hui-Pin Hsiao, 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 Personalized Medicine|July 27, 2022
Newborn Screening Program for Mucopolysaccharidosis Type II and Long-Term Follow-Up of the Screen-Positive Subjects in TaiwanHsiang-Yu Lin, Ya-Hui Chang, Chung-Lin Lee, et al.
BMJ Open|July 19, 2013
Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A)Hsiang-Yu Lin, Hao-Chuan Liu, Yu-Hsiu Huang, et al.
Molecular Genetics and Metabolism|January 14, 2015
Longitudinal analysis of endurance and respiratory function from a natural history study of Morquio A syndromePaul R Harmatz, Karl Eugen Mengel, Roberto Giugliani, et al.
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.
Human Immunology|January 9, 2007
Genetic variations of HLA-DRB1 and susceptibility to Kawasaki disease in Taiwanese childrenFu-Yuan Huang, Tzu-Yang Chang, Ming-Ren Chen, et al.
The Journal of Clinical Investigation|November 22, 2022
A phase I/II study on intracerebroventricular tralesinidase alfa in patients with Sanfilippo syndrome type BNicole Muschol, Anja Koehn, Katharina von Cossel, et al.
Pageof 29

Showing results (251-260 of 281) with videos related to

Sort By:
Pageof 29
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.
Plos One|March 22, 2014
Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic ChineseYi-Lei Wu, Daw-Yang Hwang, Hui-Pin Hsiao, 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 Personalized Medicine|July 27, 2022
Newborn Screening Program for Mucopolysaccharidosis Type II and Long-Term Follow-Up of the Screen-Positive Subjects in TaiwanHsiang-Yu Lin, Ya-Hui Chang, Chung-Lin Lee, et al.
BMJ Open|July 19, 2013
Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A)Hsiang-Yu Lin, Hao-Chuan Liu, Yu-Hsiu Huang, et al.
Molecular Genetics and Metabolism|January 14, 2015
Longitudinal analysis of endurance and respiratory function from a natural history study of Morquio A syndromePaul R Harmatz, Karl Eugen Mengel, Roberto Giugliani, et al.
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.
Human Immunology|January 9, 2007
Genetic variations of HLA-DRB1 and susceptibility to Kawasaki disease in Taiwanese childrenFu-Yuan Huang, Tzu-Yang Chang, Ming-Ren Chen, et al.
The Journal of Clinical Investigation|November 22, 2022
A phase I/II study on intracerebroventricular tralesinidase alfa in patients with Sanfilippo syndrome type BNicole Muschol, Anja Koehn, Katharina von Cossel, et al.
Pageof 29