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List of works by Jonathan M Cordeiro

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

scientific article

Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome

scientific article

Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.

scientific article

Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG

scientific article

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

scientific article

Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.

scientific article published on 03 July 2008

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

scientific article

Maximum diastolic potential of human induced pluripotent stem cell-derived cardiomyocytes depends critically on I(Kr).

scientific article

Mechanisms underlying atrial-selective block of sodium channels by Wenxin Keli: Experimental and theoretical analysis.

scientific article published on 07 January 2016

Mutation in Nav1.5 Associated with Brugada Syndrome - a Mutational Hotspot?

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

scientific article

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

scientific article published in December 2010

Ranolazine effectively suppresses atrial fibrillation in the setting of heart failure.

scientific article

Sudden death associated with short-QT syndrome linked to mutations in HERG.

scientific article

Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes

scientific article published on 01 September 2020

The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes

scientific article published in 2022

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