Myriam Berthet

Paris, France

Last Updated: 09/26/2026

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Found 9 publications

Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy.

Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy.

Journal: Circulation research

Published: March 17, 2020

Association of Serum Cholesterol Efflux Capacity With Mortality in Patients With ST-Segment Elevation Myocardial Infarction.

Association of Serum Cholesterol Efflux Capacity With Mortality in Patients With ST-Segment Elevation Myocardial Infarction.

Journal: Journal of the American College of Cardiology

Published: September 12, 2018

Differentiation and quantification of fibrosis, fat and fatty fibrosis in human left atrial myocardium using ex vivo MRI.

Differentiation and quantification of fibrosis, fat and fatty fibrosis in human left atrial myocardium using ex vivo MRI.

Journal: PloS one

Published: March 14, 2018

Cardiac MR Strain: A Noninvasive Biomarker of Fibrofatty Remodeling of the Left Atrial Myocardium.

Cardiac MR Strain: A Noninvasive Biomarker of Fibrofatty Remodeling of the Left Atrial Myocardium.

Journal: Radiology

Published: August 17, 2017

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.

Journal: European journal of human genetics : EJHG

Published: March 29, 2015

The genetics underlying acquired long QT syndrome: impact for genetic screening.

The genetics underlying acquired long QT syndrome: impact for genetic screening.

Journal: European heart journal

Published: February 25, 2015

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

Journal: Cardiovascular research

Published: January 20, 2015

Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.

Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.

Journal: Circulation. Cardiovascular genetics

Published: July 17, 2013

Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances.

Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances.

Journal: Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing

Published: December 15, 2012

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Last Updated: 09/26/2026