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Shu-Chuan Chiang

Showing results (31-40 of 39) with videos related to

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Molecular Genetics and Metabolism|July 16, 2011
Rapid progressive course of later-onset Pompe disease in Chinese patientsChih-Chao Yang, Yin-Hsiu Chien, Ni-Chung Lee, et al.
Psychiatry and Clinical Neurosciences|September 19, 2007
Analysis of association of clinical correlates and 5-HTTLPR polymorphism with suicidal behavior among Chinese methamphetamine abusersChih-Ken Chen, Shih-Ku Lin, Ming-Chyi Huang, et al.
International Journal of Neonatal Screening|September 22, 2025
Umbilical Cord Blood Sampling for Newborn Screening of Pompe Disease and the Detection of a Novel Pathogenic Variant and Pseudodeficiency Variants in an Asian PopulationFook-Choe Cheah, Sharifah Azween Syed Omar, Jasmine Lee, et al.
The Journal of Pediatrics|July 17, 2017
Presymptomatic Diagnosis of Spinal Muscular Atrophy Through Newborn ScreeningYin-Hsiu Chien, Shu-Chuan Chiang, Wen-Chin Weng, et al.
Human Mutation|July 22, 2009
Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A)Wuh-Liang Hwu, Yin-Hsiu Chien, Ni-Chung Lee, et al.
Pediatrics|December 2, 2009
Pompe disease in infants: improving the prognosis by newborn screening and early treatmentYin-Hsiu Chien, Ni-Chung Lee, Beth L Thurberg, et al.
Pediatrics|June 4, 2008
Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening programYin-Hsiu Chien, Shu-Chuan Chiang, Xiaokui Kate Zhang, et al.
JIMD Reports|February 15, 2015
Baseline Urinary Glucose Tetrasaccharide Concentrations in Patients with Infantile- and Late-Onset Pompe Disease Identified by Newborn ScreeningYin-Hsiu Chien, Jennifer L Goldstein, Wuh-Liang Hwu, et al.
Human Molecular Genetics|September 20, 2011
Human Pompe disease-induced pluripotent stem cells for pathogenesis modeling, drug testing and disease marker identificationHsiang-Po Huang, Pin-Hsun Chen, Wuh-Liang Hwu, et al.
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Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Molecular Genetics and Metabolism|July 16, 2011
Rapid progressive course of later-onset Pompe disease in Chinese patientsChih-Chao Yang, Yin-Hsiu Chien, Ni-Chung Lee, et al.
Psychiatry and Clinical Neurosciences|September 19, 2007
Analysis of association of clinical correlates and 5-HTTLPR polymorphism with suicidal behavior among Chinese methamphetamine abusersChih-Ken Chen, Shih-Ku Lin, Ming-Chyi Huang, et al.
International Journal of Neonatal Screening|September 22, 2025
Umbilical Cord Blood Sampling for Newborn Screening of Pompe Disease and the Detection of a Novel Pathogenic Variant and Pseudodeficiency Variants in an Asian PopulationFook-Choe Cheah, Sharifah Azween Syed Omar, Jasmine Lee, et al.
The Journal of Pediatrics|July 17, 2017
Presymptomatic Diagnosis of Spinal Muscular Atrophy Through Newborn ScreeningYin-Hsiu Chien, Shu-Chuan Chiang, Wen-Chin Weng, et al.
Human Mutation|July 22, 2009
Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A)Wuh-Liang Hwu, Yin-Hsiu Chien, Ni-Chung Lee, et al.
Pediatrics|December 2, 2009
Pompe disease in infants: improving the prognosis by newborn screening and early treatmentYin-Hsiu Chien, Ni-Chung Lee, Beth L Thurberg, et al.
Pediatrics|June 4, 2008
Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening programYin-Hsiu Chien, Shu-Chuan Chiang, Xiaokui Kate Zhang, et al.
JIMD Reports|February 15, 2015
Baseline Urinary Glucose Tetrasaccharide Concentrations in Patients with Infantile- and Late-Onset Pompe Disease Identified by Newborn ScreeningYin-Hsiu Chien, Jennifer L Goldstein, Wuh-Liang Hwu, et al.
Human Molecular Genetics|September 20, 2011
Human Pompe disease-induced pluripotent stem cells for pathogenesis modeling, drug testing and disease marker identificationHsiang-Po Huang, Pin-Hsun Chen, Wuh-Liang Hwu, et al.
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