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The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia

Leukemia, 2018-04, Vol.32 (4), p.911-919

2018

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The Cul4A–DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activity

Oncogene, 2013-09, Vol.32 (39), p.4721-4726

2013

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Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

Circulation research, 2001-04, Vol.88 (7), p.740-745

2001

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Unexpectedly high prevalence of structural genomic variations in the Long QT Syndrome: evidence for broader clinical uptake

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Implantable loop recorder monitoring in inherited cardiomyopathies: yield of clinically relevant arrhythmias

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Catecholaminergic polymorphic ventricular tachycardia: risk modulators in patients treated with beta-blockers

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Natural History of Patients with Typical and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Efficacy and safety of the ICD in patients with catecholaminergic polymorphic ventricular tachycardia

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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Mutation site-specific risk profile in patients with Type 1 Long QT Syndrome

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Cell, 2003-06, Vol.113 (7), p.829-840

2003

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Role of CACNA1C variants in Brugada syndrome: clinical aspects and genetic testing strategies

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region

Human immunology, 2001-09, Vol.62 (9), p.871-884

2001

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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2001-01, Vol.103 (2), p.196-200

2001

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6081Efficacy and limitations of quinidine therapy in patients with Brugada Syndrome

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

2019

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Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2002-07, Vol.106 (1), p.69-74

2002

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Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

Journal of cellular physiology, 2002-01, Vol.190 (1), p.1-6

2002

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Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes

The Journal of biological chemistry, 2001-08, Vol.276 (33), p.30623-30630

2001

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Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Annals of human genetics, 2000-09, Vol.64 (5), p.395-412

2000

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Brugada syndrome and sudden cardiac death in children

The Lancet (British edition), 2000-03, Vol.355 (9206), p.808-809

2000

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Genetic structure and affinities of the corsican population (France): Classical genetic markers analysis

American journal of human biology, 2003-03, Vol.15 (2), p.151-163

2003

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Mitochondrial control-region sequence variation in the Corsican population, France

American journal of human biology, 2000-05, Vol.12 (3), p.339-351

2000

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The application of Diamond Exploration Geoscientific Information System (DEGIS) technology for integrated diamond exploration in the north-central United States of America

International journal of remote sensing, 1997-05, Vol.18 (7), p.1439-1464

1997

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Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome

American journal of physiology. Heart and circulatory physiology, 2000-10, Vol.279 (4), p.H1748-H1756

2000

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Mechanisms of I Ks suppression in LQT1 mutants

American journal of physiology. Heart and circulatory physiology, 2000-12, Vol.279 (6), p.H3003-H3011

2000

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The E3 ubiquitin ligase WWP1 sustains the growth of acute myeloid leukaemia

Le social à l’épreuve du dégoût

The Cul4A–DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activity

Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel

Unexpectedly high prevalence of structural genomic variations in the Long QT Syndrome: evidence for broader clinical uptake

Implantable loop recorder monitoring in inherited cardiomyopathies: yield of clinically relevant arrhythmias

Catecholaminergic polymorphic ventricular tachycardia: risk modulators in patients treated with beta-blockers

Natural History of Patients with Typical and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia

Efficacy and safety of the ICD in patients with catecholaminergic polymorphic ventricular tachycardia

Mutation site-specific risk profile in patients with Type 1 Long QT Syndrome

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Role of CACNA1C variants in Brugada syndrome: clinical aspects and genetic testing strategies

Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

6081Efficacy and limitations of quinidine therapy in patients with Brugada Syndrome

Clinical and molecular characterization of Patients with catecholaminergic polymorphic ventricular tachycardia

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia

Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes

Patterns of male-specific inter-population divergence in Europe, West Asia and North Africa

Brugada syndrome and sudden cardiac death in children

Genetic structure and affinities of the corsican population (France): Classical genetic markers analysis

Mitochondrial control-region sequence variation in the Corsican population, France

The application of Diamond Exploration Geoscientific Information System (DEGIS) technology for integrated diamond exploration in the north-central United States of America

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome

Mechanisms of I Ks suppression in LQT1 mutants

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