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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Circulation (New York, N.Y.), 2010-02, Vol.121 (5), p.635-643

2010

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Dysfonctions sinusales : mécanismes physiopathologiques

Archives des maladies du coeur et des vaisseaux. Pratique, 2012-11, Vol.2012 (212), p.27-30

Le Marec, H.

2012

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Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

Europace (London, England), 2013-12, Vol.15 (12), p.1805-1811

2013

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Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

Biochimica et biophysica acta, 2014-02, Vol.1843 (2), p.234-244

2014

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Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern

Heart rhythm, 2008-11, Vol.5 (11), p.1561-1564

2008

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G024 Implication des canaux KATP dans le syndrome de repolarisation précoce

Archives of cardiovascular diseases, 2009, Vol.102, p.S70-S71

2009

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Cardiac conduction defects associate with mutations in SCN5A

Nature genetics, 1999-09, Vol.23 (1), p.20-21

1999

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GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Heart rhythm, 2014-11, Vol.11 (11), p.2133-2133

2014

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Génétique de la fibrillation auriculaire

Annales de cardiologie et d'angéiologie, 2009-12, Vol.58, p.S70-S72

2009

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Actualité sur la génétique du prolapsus valvulaire mitral

Archives des maladies du coeur et des vaisseaux. Pratique, 2014-12, Vol.2014 (233), p.28-30

2014

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The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

Journal of medical genetics, 2003-02, Vol.40 (2), p.141-145

2003

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Do inherited prothrombotic factors have a role in myocardial infarction with normal coronary arteriogram?

Journal of internal medicine, 1998-12, Vol.244 (6), p.543-544

1998

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Nature (London), 2003-02, Vol.421 (6923), p.634-639

2003

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Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization

Neurology, 2003-01, Vol.60 (2), p.340-342

2003

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P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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The Effect of Cardiac Resynchronization on Morbidity and Mortality in Heart Failure

The New England journal of medicine, 2005-04, Vol.352 (15), p.1539-1549

2005

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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family

Circulation (New York, N.Y.), 2001-12, Vol.104 (25), p.3081-3086

2001

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Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

PloS one, 2010-02, Vol.5 (2), p.e9298-e9298

2010

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Alterations in the force‐frequency relationship by tert‐ butylbenzohydroquinone, a putative SR Ca2+ pump inhibitor, in rabbit and rat ventricular muscle

British journal of pharmacology, 1996-01, Vol.117 (2), p.258-267

1996

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Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study

European heart journal, 2012-03, Vol.33 (5), p.622-629

2012

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P5441Aortic valve phenotype associated with filamin-A mutations: a comprehensive echocardiographic and outcomes analyses

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

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G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome

Archives of cardiovascular diseases, 2009, Vol.102, p.S70-S70

2009

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Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Journal of the American College of Cardiology, 2003-02, Vol.41 (4), p.643-652

2003

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Familial aggregation of calcific aortic valve stenosis in the western part of France

Circulation (New York, N.Y.), 2006-02, Vol.113 (6), p.856-860

2006

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Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype

European heart journal, 2001-03, Vol.22 (5), p.410-422

2001

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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Dysfonctions sinusales : mécanismes physiopathologiques

Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern

G024 Implication des canaux KATP dans le syndrome de repolarisation précoce

Cardiac conduction defects associate with mutations in SCN5A

GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME

Génétique de la fibrillation auriculaire

Actualité sur la génétique du prolapsus valvulaire mitral

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome

Do inherited prothrombotic factors have a role in myocardial infarction with normal coronary arteriogram?

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization

P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation

The Effect of Cardiac Resynchronization on Morbidity and Mortality in Heart Failure

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family

Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model

Alterations in the force‐frequency relationship by tert‐ butylbenzohydroquinone, a putative SR Ca2+ pump inhibitor, in rabbit and rat ventricular muscle

Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study

P5441Aortic valve phenotype associated with filamin-A mutations: a comprehensive echocardiographic and outcomes analyses

G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

Familial aggregation of calcific aortic valve stenosis in the western part of France

Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype

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