Chien-Chih Chang

发表

Experience of pentavalent human-bovine reassortant rotavirus vaccine among healthy infants in Taiwan.

Mei-Hwei Chang, P. Lee, W. Hsieh, 2009, Journal of the Formosan Medical Association = Taiwan yi zhi.

Coronary Artery Anatomy in Complete Transposition with Situs Solitus and Dextrocardia

I. Chiu, Chun-An Chen, H. Chiu, 2010, Pediatric Cardiology.

Special electrophysiological characteristics of pediatric idiopathic ventricular tachycardia.

S. Chiu, Jou-Kou Wang, Mei-Hwan Wu, 2017, International journal of cardiology.

Transmission of acute infectious illness among cases of Kawasaki disease and their household members.

P. Shao, Luan-Yin Chang, Li-Min Huang, 2015, Journal of the Formosan Medical Association = Taiwan yi zhi.

Viral infections associated with Kawasaki disease

P. Shao, Luan-Yin Chang, Li-Min Huang, 2014, Journal of the Formosan Medical Association.

Radiofrequency catheter ablation of supraventricular tachycardia in infants and toddlers.

Jiunn-lee Lin, S. Chiu, Jou-Kou Wang, 2009, Circulation journal : official journal of the Japanese Circulation Society.

Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events

M. Chahine, S. Chiu, Jou-Kou Wang, 2012, Human Genetics.

Balloon Valvuloplasty as an Initial Palliation in the Treatment of Newborns and Young Infants with Severely Symptomatic Tetralogy of Fallot

E. Wu, Jou-Kou Wang, Mei-Hwan Wu, 2005, Cardiology.

Radiofrequency Catheter Ablation of Atrial Tachyarrhythmias in Adults with Repaired Congenital Heart Disease: Constraints from Multiple and New Arrhythmic Foci.

Jiunn-lee Lin, Chia-Ti Tsai, S. Chiu, 2013, Acta Cardiologica Sinica.

Mediastinal and retropharyngeal abscesses in a neonate.

R. Lien, M. Chiang, Chao-Jan Wang, 2011, Pediatrics and Neonatology.

Clinical Implication of the C Allele of the ITPKC Gene SNP rs28493229 in Kawasaki Disease: Association With Disease Susceptibility and BCG Scar Reactivation

Chien-Chih Chang, Pei-Lung Chen, J. Yeh, 2011, The Pediatric infectious disease journal.

Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events

M. Chahine, S. Chiu, Jou-Kou Wang, 2012, Human Genetics.

A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia.

F. Chiang, M. Chahine, Jou-Kou Wang, 2004, Cardiovascular research.

Postnatal outcome of fetal cardiac echogenic foci.

F. Hsieh, Chien-Nan Lee, M. Shyu, 2002, Journal of the Formosan Medical Association = Taiwan yi zhi.

Utero Onset of Long QT Syndrome with Atrioventricular Block and Spontaneous or Lidocaine-induced Ventricular Tachycardia : compound effects of hERG pore-region mutation and SCN 5 A N-terminus variant

E. Ficker, G. Christé, M. Chahine, 2009 .

In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant.

E. Ficker, G. Christé, M. Chahine, 2008, Heart rhythm.