Elena Burashnikov

发表

Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERG

J. Brugada, R. Brugada, C. Antzelevitch, 2003, Circulation.

Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome.

J. Brugada, R. Brugada, P. Brugada, 2005, Journal of molecular and cellular cardiology.

Coexistence of atrioventricular accessory pathways and drug‐induced type 1 Brugada pattern

C. Antzelevitch, Elena Burashnikov, M. Orman, 2018, Pacing and clinical electrophysiology : PACE.

Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel

C. Antzelevitch, R. Beinart, M. Glikson, 2019, Front. Physiol..

Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

C. Antzelevitch, M. Borggrefe, C. Wolpert, 2016, Journal of the American Heart Association.

Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: Expanding the spectrum of Timothy syndrome

C. Antzelevitch, D. Chitayat, S. Blaser, 2012, American journal of medical genetics. Part A.

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents.

P. Schwartz, C. Antzelevitch, M. Borggrefe, 2012, Heart rhythm.

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8.

C. Antzelevitch, M. Borggrefe, M. Haïssaguerre, 2012, Heart rhythm.

Biophysical and Molecular Characterization of a Novel De Novo KCNJ2 Mutation Associated With Andersen-Tawil Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia Mimicry

C. Antzelevitch, Elena Burashnikov, H. Barajas-Martinez, 2011, Circulation. Cardiovascular genetics.

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction.

R. Brugada, S. Viskin, C. Antzelevitch, 2007, Heart rhythm.

Value of Electrocardiographic Parameters and Ajmaline Test in the Diagnosis of Brugada Syndrome Caused by SCN5A Mutations

J. Towbin, J. Brugada, R. Brugada, 2004, Circulation.

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

Martin Borggrefe, Ryan Pfeiffer, Dan Hu, 2010, Heart rhythm.

A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

C. Antzelevitch, J. Cordeiro, G. Pollevick, 2009, Circulation. Cardiovascular genetics.

Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome

Jørgen K. Kanters, C. Antzelevitch, J. Cordeiro, 2008, Circulation. Arrhythmia and electrophysiology.

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

Michel Haïssaguerre, Antonio Oliva, Martin Borggrefe, 2007, Circulation.

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.

J. Svendsen, C. Antzelevitch, J. Cordeiro, 2008, Heart rhythm.

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.

Frank Sachse, Antonio Oliva, Josep Brugada, 2005, Cardiovascular research.

LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.

C. Antzelevitch, M. Eldar, M. Glikson, 2011, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.

C. Antzelevitch, Elena Burashnikov, C. Hasdemir, 2015, Heart rhythm.

Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome.

K. Vernooy, T. Delhaas, R. Brugada, 2006, Heart rhythm.

Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome.

Ryan Pfeiffer, Charles Antzelevitch, Jonathan M Cordeiro, 2009, Journal of molecular and cellular cardiology.

ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

C. Antzelevitch, M. Borggrefe, A. Terzic, 2014, International journal of cardiology.

Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome

Ryan Pfeiffer, Dan Hu, Charles Antzelevitch, 2010, Pacing and clinical electrophysiology : PACE.

SCN5A mutation associated with acute myocardial infarction.

V. Pascali, R. Brugada, S. Viskin, 2009, Legal medicine.

Mutations in the Cardiac L-Type Calcium Channel Associated with Inherited Sudden Cardiac Death Syndromes

S. Viskin, C. Antzelevitch, M. Borggrefe, 2010 .

A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death

C. Antzelevitch, J. Cordeiro, K. Calloe, 2010, Circulation. Cardiovascular genetics.

Compound Heterozygous Mutations P336L and I1660V in the Human Cardiac Sodium Channel Associated With the Brugada Syndrome

J. Brugada, R. Brugada, C. Antzelevitch, 2006, Circulation.

Abstract 1929: Mutations in the Cardiac L-Type Calcium Channel Associated With Four Sudden Cardiac Death Syndromes

S. Viskin, C. Antzelevitch, M. Borggrefe, 2009 .

Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.

Martin Borggrefe, Ryan Pfeiffer, Charles Antzelevitch, 2010, Canadian journal of physiology and pharmacology.