|
|
Multicenter Experience With Catheter Ablation for Ventricular Tachycardia in Lamin A/C Cardiomyopathy
Saurabh Kumar
,
Alexander F.A. Androulakis
,
Jean-Marc Sellal
,
Philippe Maury
,
Estelle Gandjbakhch
,
et al.
Journal articles
hal-03233139v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
FHL2 expression and variants in hypertrophic cardiomyopathy
Felix W. Friedrich
,
Silke Reischmann
,
Aileen Schwalm
,
Andrea Unger
,
Deepak Ramanujam
,
et al.
Journal articles
hal-01110561v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations
Julien Thevenon
,
Gabriel Laurent
,
Flavie Ader
,
Pascal Laforêt
,
Didier Klug
,
et al.
Journal articles
hal-01444277v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods
Pascal Amedro
,
Oscar Werner
,
Hamouda Abassi
,
Aymeric Boisson
,
Luc Souilla
,
et al.
Journal articles
hal-03310460v2
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Prognosis of Adults With Isolated Left Ventricular Non-Compaction: Results of a Prospective Multicentric Study
Hilla Gerard
,
Nicolas Iline
,
Hélène Martel
,
Karine Nguyen
,
Pascale Richard
,
et al.
Journal articles
hal-03999097v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure
Mohammed Majid Akhtar
,
Massimiliano Lorenzini
,
Menelaos Pavlou
,
Juan Pablo Ochoa
,
Constantinos O’mahony
,
et al.
Journal articles
hal-03280888v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations
Flavie Ader
,
Pascal de Groote
,
Patricia Réant
,
Caroline Rooryck-Thambo
,
Delphine Dupin-Deguine
,
et al.
Journal articles
hal-02268422v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity
Pascale Richard
,
Flavie Ader
,
Maguelonne Roux
,
Erwan Donal
,
Jean-Christophe Eicher
,
et al.
Journal articles
hal-02055778v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Joel Fedida
,
Veronique Fressart
,
Philippe Charron
,
Elodie Surget
,
Tiphaine Hery
,
et al.
Journal articles
hal-01579640v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy
Isabelle Marey
,
Véronique Fressart
,
Caroline Rambaud
,
Paul Fornès
,
Laurent Martin
,
et al.
Journal articles
hal-02898070v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.
Nathalie Roux-Buisson
,
Estelle Gandjbakhch
,
Erwan Donal
,
Vincent Probst
,
Jean-Claude Deharo
,
et al.
Heart Rhythm, 2014, pp.1999-2009
Journal articles
inserm-01120324v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT Study
Celine Bordet
,
Sandrine Brice
,
Carole Maupain
,
Estelle Gandjbakhch
,
Bertrand Isidor
,
et al.
Journal articles
hal-02882035v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction
Marie Cambon-Viala
,
Hilla Gerard
,
Karine Nguyen
,
Pascale Richard
,
Flavie Ader
,
et al.
Journal articles
hal-04073195v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Ulrike Esslinger
,
Sophie Garnier
,
Agathe Korniat
,
Carole Proust
,
Georgios Kararigas
,
et al.
Journal articles
hal-02949402v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Inherited Cardiomyopathies Revealed by Clinically Suspected Myocarditis
Flavie Ader
,
Elodie Surget
,
Philippe Charron
,
Alban Redheuil
,
Amir Zouaghi
,
et al.
Journal articles
inserm-03996719v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Genotype-phenotype correlations of pathogenic variants in the FLNC gene
Flavie Ader
,
Eric Villard
,
Céline Ledeuil
,
Philippe Charron
,
Pascale Richard
Journal articles
inserm-03996754v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Natural history of Barth syndrome: a national cohort study of 22 patients.
Charlotte Rigaud
,
Anne-Sophie Lebre
,
Renaud Touraine
,
Blandine Beaupain
,
Chris Ottolenghi
,
et al.
Journal articles
inserm-00823569v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
External validation of risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers
Marine Thuillot
,
Carole Maupain
,
Estelle Gandjbakhch
,
Xavier Waintraub
,
Françoise Hidden-Lucet
,
et al.
Journal articles
hal-02153574v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
Veronique Fressart
,
Guillaume Duthoit
,
Erwan Donal
,
Vincent Probst
,
Jean-Claude Deharo
,
et al.
Journal articles
inserm-00588266v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
The Public Health Burden of Cardiomyopathies: Insights from a Nationwide Inpatient Study
Simon Lannou
,
Nicolas Mansencal
,
Cécile Couchoud
,
Mathilde Lassalle
,
Olivier Dubourg
,
et al.
Journal articles
hal-02883447v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients
Sophie Garnier
,
Christian Hengstenberg
,
Nicolas Lamblin
,
Olivier Dubourg
,
Pascal de Groote
,
et al.
Journal articles
hal-01143379v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Global and regional echocardiographic strain to assess the early phase of hypertrophic cardiomyopathy due to sarcomeric mutations
Guillaume Baudry
,
Nicolas Mansencal
,
Amélie Reynaud
,
Pascale Richard
,
Olivier Dubourg
,
et al.
Journal articles
hal-02883415v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Saw-Tooth Cardiomyopathy: Clinical Presentation and Genetic Analysis
Julie Proukhnitzky
,
Jérôme Garot
,
Céline Bordet
,
Lise Legrand
,
Flavie Ader
,
et al.
Journal articles
inserm-03996698v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
The value of electrocardiography and echocardiography in distinguishing Fabry disease from sarcomeric hypertrophic cardiomyopathy
Nicolas Junqua
,
Damien Legallois
,
Sophie Segard
,
Olivier Lairez
,
Patricia Réant
,
et al.
Journal articles
hal-02945476v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Prevalence of familial hypercholesterolaemia in patients presenting with premature acute coronary syndrome
Marie Hauguel-Moreau
,
Vincent Aïdan
,
Hélène Hergault
,
Alain Beauchet
,
Marion Pépin
,
et al.
Journal articles
hal-04006296v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition
Marie Gizon
,
Laëtitia Duboscq-Bidot
,
Lina El Kassar
,
Pierre Bobin
,
Flavie Ader
,
et al.
Journal articles
hal-03549731v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy.
Gabriel Laurent
,
Samuel Saal
,
Mohamed Yassine Amarouch
,
Delphine M. Béziau
,
Roos F. J. Marsman
,
et al.
Journal articles
inserm-00719034v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy
Karine Nguyen
,
Stéphane Roche
,
Erwan Donal
,
Sylvie Odent
,
Jean-Christophe Eicher
,
et al.
Journal articles
hal-02140150v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches
Mine Arslan-Kirchner
,
Eloisa Arbustini
,
Catherine Boileau
,
Philippe Charron
,
Anne Child
,
et al.
Journal articles
hal-01670149v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
Ulrike Esslinger
,
Sophie Garnier
,
Agathe Korniat
,
Carole Proust
,
Georgios Kararigas
,
et al.
Journal articles
hal-03571195v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|