Similarities and differences of clinical characteristics between Brugada syndrome and early repolarization syndrome

This publication has 35 references indexed in Scilit:

• Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
  Heart Rhythm, 2012
• Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
  Heart Rhythm, 2010
• J wave syndromes
  Heart Rhythm, 2010
• Mode of onset of ventricular fibrillation in patients with early repolarization pattern vs. Brugada syndrome
  European Heart Journal, 2009
• A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype
  Circulation: Cardiovascular Genetics, 2009
• Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene ( GPD1-L ) Mutations in Sudden Infant Death Syndrome
  Circulation, 2007
• Occurrence of “J Waves” in 12‐Lead ECG as a Marker of Acute Ischemia and Their Cellular Basis
  Pacing and Clinical Electrophysiology, 2007
• Loss-of-Function Mutations in the Cardiac Calcium Channel Underlie a New Clinical Entity Characterized by ST-Segment Elevation, Short QT Intervals, and Sudden Cardiac Death
  Circulation, 2007
• Recurrent syncope in a patient with prominent J wave
  American Heart Journal, 1994
• Idiopathic ventricular fibrillation and bradycardia-dependent intraventricular block
  American Heart Journal, 1993