C. Chiang

发表

Detecting multiple lysosomal storage diseases by tandem mass spectrometry--a national newborn screening program in Taiwan.

F. Tsai, Yann‐Jang Chen, D. Niu, 2014, Clinica chimica acta; international journal of clinical chemistry.

Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A)

Shih-Jen Chen, Hsiang-Yu Lin, Shuan-Pei Lin, 2010, Journal of Inherited Metabolic Disease.

Nationwide survey of extended newborn screening by tandem mass spectrometry in Taiwan

Yin-Hsiu Chien, Wuh-Liang Hwu, Shu-Min Kao, 2010, Journal of Inherited Metabolic Disease.

Low birth weight and high birth weight infants are both at an increased risk to have type 2 diabetes among schoolchildren in taiwan.

L. Chuang, F. Sung, R. Lin, 2003, Diabetes care.

Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2018, Orphanet Journal of Rare Diseases.

Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A)

Hsiang-Yu Lin, Shuan-Pei Lin, D. Niu, 2013, BMJ Open.

Clinical observations on enzyme replacement therapy in patients with Fabry disease and the switch from agalsidase beta to agalsidase alfa

Hsiang-Yu Lin, Shuan-Pei Lin, D. Niu, 2014, Journal of the Chinese Medical Association : JCMA.

Screening for diabetes in asymptomatic children: A simple and efficient method.

L. Chuang, F. Sung, Wan-Chen Wu, 2020, Journal of the Formosan Medical Association = Taiwan yi zhi.

Obesity and clustering of cardiovascular disease risk factors are associated with elevated plasma complement C3 in children and adolescents

A. Carter, L. Chuang, F. Sung, 2012, Pediatric diabetes.

Newborn Screening for Methylmalonic Aciduria by Tandem Mass Spectrometry: 7 Years' Experience From Two Centers in Taiwan

W. Hwu, K. Hsiao, Hsiang-Yu Lin, 2010, Journal of the Chinese Medical Association : JCMA.

Birth weight and type 1 diabetes among schoolchildren in Taiwan--A population-based case-controlled study.

L. Chuang, F. Sung, Chung-Yi Li, 2006, Diabetes research and clinical practice.

Functional and biological studies of α-galactosidase A variants with uncertain significance from newborn screening in Taiwan.

D. Niu, Chun-kai Huang, Hsuan-Chieh Liao, 2017, Molecular genetics and metabolism.

Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A).

Wen-Chung Yu, F. Tsai, C. Fann, 2013, Clinica chimica acta; international journal of clinical chemistry.

High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese Population

Shing‐Jong Lin, Hsiang-Yu Lin, C. Hsueh, 2009, Circulation. Cardiovascular genetics.

Later Onset Fabry Disease, Cardiac Damage Progress in Silence: Experience With a Highly Prevalent Mutation.

Wen-Chung Yu, R. Desnick, Hsiang-Yu Lin, 2016, Journal of the American College of Cardiology.

Very rare condition of multiple Gaucheroma: A case report and review of the literature

W. Soong, Y. Yeh, D. Niu, 2019, Molecular genetics and metabolism reports.

Very Early Treatment for Infantile-Onset Pompe Disease Contributes to Better Outcomes.

W. Soong, Chih-jou Lai, D. Niu, 2016, The Journal of pediatrics.

A large‐scale nationwide newborn screening program for pompe disease in Taiwan: Towards effective diagnosis and treatment

Chih-jou Lai, D. Niu, Hui-Chen Ho, 2014, American journal of medical genetics. Part A.

Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI

M. Gelb, Hsiang-Yu Lin, Shuan-Pei Lin, 2019, The Journal of pediatrics.

Mass Spectrometry but Not Fluorimetry Distinguishes Affected and Pseudodeficiency Patients in Newborn Screening for Pompe Disease.

M. Gelb, D. Niu, Chun-kai Huang, 2017, Clinical chemistry.

Very rare condition of multiple Gaucheroma: A case report and review of the literature☆

W. Soong, Y. Yeh, D. Niu, 2019, Molecular genetics and metabolism reports.

Endomyocardial biopsies in patients with left ventricular hypertrophy and a common Chinese later-onset fabry mutation (IVS4 + 919G > A)

Wen-Chung Yu, Hsiang-Yu Lin, S. Sung, 2014, Orphanet Journal of Rare Diseases.

National surveillance for type 2 diabetes mellitus in Taiwanese children.

L. Chuang, F. Sung, R. Lin, 2003, JAMA.

Detecting 22q11.2 Deletion Syndrome in Newborns with Low T Cell Receptor Excision Circles from Severe Combined Immunodeficiency Screening

S. Kao, Hsuan-Chieh Liao, C. Chiang, 2019, The Journal of pediatrics.

Elevated blood pressure, obesity, and hyperlipidemia.

K. Chien, F. Sung, T. Su, 2009, The Journal of pediatrics.

Hypertension and hypercholesterolemia aggregate in nondiabetic children and adolescents with higher fasting plasma glucose levels

L. Chuang, F. Sung, Mao-Shin Lin, 2011, Pediatric diabetes.

Newborn Screening for Vitamin B6 Non-responsive Classical Homocystinuria: Systematical Evaluation of a Two-Tier Strategy.

J. Okun, G. Hoffmann, P. Burgard, 2016, JIMD reports.

Methylmalonic acidemia/propionic acidemia – the biochemical presentation and comparing the outcome between liver transplantation versus non-liver transplantation groups

M. Ho, Y. Chien, W. Hwu, 2019, Orphanet Journal of Rare Diseases.

T. Tai, L. Chuang, F. Sung, 2004, Diabetes care.

Birth Weight Correlates Differently with Cardiovascular Risk Factors in Youth

L. Chuang, F. Sung, Chung-Yi Li, 2007, Obesity.