Loss-of-functionKCNH2mutation in a family with long QT syndrome, epilepsy, and sudden death

Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation

(2013) Pasquale Parisi et al.   EPILEPSY RESEARCH

KCNH2 Gene Mutation: A Potential Link Between Epilepsy and Long QT-2 Syndrome

(2012) José J. Zamorano-León et al.   JOURNAL OF NEUROGENETICS

Concealed Long QT Syndrome and Intractable Partial Epilepsy: A Case Report

(2012) Jason H. Anderson et al.   MAYO CLINIC PROCEEDINGS

Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures

(2011) Dagmar I. Keller et al.   CANADIAN JOURNAL OF CARDIOLOGY

Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases

(2010) Emily Tu et al.   BRAIN PATHOLOGY

Kv1.1 Potassium Channel Deficiency Reveals Brain-Driven Cardiac Dysfunction as a Candidate Mechanism for Sudden Unexplained Death in Epilepsy

(2010) E. Glasscock et al.   JOURNAL OF NEUROSCIENCE

Pathologic cardiac repolarization in pharmacoresistant epilepsy and its potential role in sudden unexpected death in epilepsy: A case-control study

(2009) Rainer Surges et al.   EPILEPSIA

Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?

(2009) Sarah E. Heron et al.   EPILEPSIA

Genotype-Phenotype Aspects of Type 2 Long QT Syndrome

(2009) Wataru Shimizu et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Sudden unexpected death in epilepsy: risk factors and potential pathomechanisms

(2009) Rainer Surges et al.   Nature Reviews Neurology

Self-Limited Hyperexcitability: Functional Effect of a Familial Hemiplegic Migraine Mutation of the Nav1.1 (SCN1A) Na+ Channel

(2008) S. Cestele et al.   JOURNAL OF NEUROSCIENCE

Sudden unexpected death in epilepsy: current knowledge and future directions

(2008) Torbjörn Tomson et al.   LANCET NEUROLOGY

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

(2008) J. N. Johnson et al.   NEUROLOGY