Cheng‐Hung Huang

发表

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.

Six new mutations of the thyroglobulin gene discovered in taiwanese children presenting with thyroid dyshormonogenesis.

T. Jap, D. Niu, Hsiao-Chi Yu, 2009, The Journal of clinical endocrinology and metabolism.

Clinical observations, molecular genetic analysis, and treatment of sitosterolemia in infants and children

L. Ho, C. Kwok, D. Niu, 2010, Journal of Inherited Metabolic Disease.

The killer cell immunoglobulin-like receptor genes do not confer susceptibility to psoriasis vulgaris independently in Chinese.

S. Tsai, Ming-Wei Lin, Yung-Ting Chang, 2006, The Journal of investigative dermatology.

Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome

Chi-Jung Huang, M. Cheong, C. Chien, 2009, BMC Medical Genetics.

Clinical observations and treatment of pediatric homozygous familial hypercholesterolemia due to a low-density lipoprotein receptor defect.

M. Charng, D. Niu, Hao-Chuan Liu, 2015, Journal of clinical lipidology.

Using Desmoglein 1 and 3 Enzyme‐linked Immunosorbent Assay as an Adjunct Diagnostic Tool for Pemphigus

Yung-Ting Chang, Cheng-Hung Huang, Chih-Chiang Chen, 2007, Journal of the Chinese Medical Association : JCMA.

Histopathological and immunohistochemical studies of poroid hidradenoma

Yung-Ting Chang, Chih-Chiang Chen, Han-Nan Liu, 2005, Archives of Dermatological Research.

Effects of Growth Hormone Treatment on Height, Weight, and Obesity in Taiwanese Patients with Prader‐Willi Syndrome

F. Tsai, P. Kuo, Hsiang-Yu Lin, 2008, Journal of the Chinese Medical Association : JCMA.

Painful swelling of the left elbow in a uraemic patient.

Wu-chang Yang, A. Yang, Jinn-Yang Chen, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Growth Hormone Therapy in Neonatal Patients With Methylmalonic Acidemia

K. Hsiao, Hsiang-Yu Lin, Tze-tze Liu, 2009, Journal of the Chinese Medical Association : JCMA.

Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2.

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2010, Human genetics.

Junctional epidermolysis bullosa.

Chih‐Yi Hsu, A. Yang, B. Hwang, 2006, Journal of the Chinese Medical Association : JCMA.

The genetic polymorphisms of POU5F1 gene are associated with psoriasis vulgaris in Chinese.

S. Tsai, Ming-Wei Lin, Yung-Ting Chang, 2007, Journal of dermatological science.

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.

Clinical observations and treatment of pediatric homozygous familial hypercholesterolemia due to a low-density lipoprotein receptor defect.

M. Charng, D. Niu, Hao-Chuan Liu, 2015, Journal of clinical lipidology.

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.

Junctional epidermolysis bullosa.

C. Kao, Sue Chen, An-Hang Yang, 2006, Journal of the Chinese Medical Association : JCMA.