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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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Effect of dissolved oxygen concentration on microalgal culture in photobioreactors

Algal research (Amsterdam), 2019-05, Vol.39, p.101432, Article 101432

2019

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Investigation of the photosynthetic response of Chlorella vulgaris to light changes in a torus-shape photobioreactor

Applied microbiology and biotechnology, 2021-12, Vol.105 (23), p.8689-8701

2021

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Development and validation of a screening procedure of microalgae for biodiesel production: Application to the genus of marine microalgae Nannochloropsis

Bioresource technology, 2015-02, Vol.177, p.224-232

2015

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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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Effect of design dark fraction on the loss of biomass productivities in photobioreactors

Bioprocess and biosystems engineering, 2020-02, Vol.43 (2), p.207-216

2020

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Development and validation of a screening system for characterizing and modeling biomass production from cyanobacteria and microalgae: Application to Arthrospira platensis and Haematococcus pluvialis

Algal research (Amsterdam), 2021-10, Vol.58, p.102386, Article 102386

2021

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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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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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Cardiac conduction defects associate with mutations in SCN5A

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

1999

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Investigation of growth limitation by CO2 mass transfer and inorganic carbon source for the microalga Chlorella vulgaris in a dedicated photobioreactor

Chemical engineering science, 2021-04, Vol.233, p.116388, Article 116388

2021

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

Effect of dissolved oxygen concentration on microalgal culture in photobioreactors

Investigation of the photosynthetic response of Chlorella vulgaris to light changes in a torus-shape photobioreactor

Development and validation of a screening procedure of microalgae for biodiesel production: Application to the genus of marine microalgae Nannochloropsis

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

Effect of design dark fraction on the loss of biomass productivities in photobioreactors

Development and validation of a screening system for characterizing and modeling biomass production from cyanobacteria and microalgae: Application to Arthrospira platensis and Haematococcus pluvialis

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

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

Cardiac conduction defects associate with mutations in SCN5A

Investigation of growth limitation by CO2 mass transfer and inorganic carbon source for the microalga Chlorella vulgaris in a dedicated photobioreactor

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

Dysfonctions sinusales : mécanismes physiopathologiques

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

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

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

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

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

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

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

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