Cardiac Channelopathies Associated with Infantile Fatal Ventricular Arrhythmias: From the Cradle to the Bench

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

(2013) Lia Crotti et al.   CIRCULATION

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

(2012) Mette Nyegaard et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children

(2012) Priya Chockalingam et al.   HEART RHYTHM

The human Nav1.5 F1486 deletion associated with long QT syndrome leads to impaired sodium channel inactivation and reduced lidocaine sensitivity

(2012) Weihua Song et al.   JOURNAL OF PHYSIOLOGY-LONDON

Brugada-Like Syndrome in Infancy Presenting With Rapid Ventricular Tachycardia and Intraventricular Conduction Delay

(2011) Ronald J. Kanter et al.   CIRCULATION

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents

(2011) Dan Hu et al.   HEART RHYTHM

Cardiac ion channel mutations in the sudden infant death syndrome

(2011) Eva C. Klaver et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Sudden infant death syndrome–associated mutations in the sodium channel beta subunits

(2010) Bi-Hua Tan et al.   HEART RHYTHM

Clinical Characteristics and Genetic Background of Congenital Long-QT Syndrome Diagnosed in Fetal, Neonatal, and Infantile Life

(2009) Hitoshi Horigome et al.   Circulation-Arrhythmia and Electrophysiology

A novel SCN5A mutation associated with the linker between III and IV domains of Nav1.5 in a neonate with fatal long QT syndrome

(2009) Kenichiro Yamamura et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Congenital long QT syndrome

(2008) Lia Crotti et al.   Orphanet Journal of Rare Diseases

Cardiac Ion Channel Gene Mutations in Sudden Infant Death Syndrome

(2008) Tesshu Otagiri et al.   PEDIATRIC RESEARCH