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Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

European heart journal, 2005-04, Vol.26 (8), p.794-803

2005

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Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

European heart journal, 2009-09, Vol.30 (17), p.2128-2136

2009

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Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy

Journal of the American College of Cardiology, 2012-11, Vol.60 (19), p.1916-1920

2012

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Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases

European heart journal, 2008-01, Vol.29 (2), p.270-276

2008

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Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

Circulation (New York, N.Y.), 1998-06, Vol.97 (22), p.2230-2236

1998

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Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

European heart journal, 2010-11, Vol.31 (22), p.2715-2726

2010

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Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population

Circulation (New York, N.Y.), 1997-07, Vol.96 (1), p.214-219

1997

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Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study

Journal of the American College of Cardiology, 2012-01, Vol.59 (5), p.493-500

2012

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The Genetic Bases of Cardiomyopathies

Journal of the American College of Cardiology, 2006-11, Vol.48 (9), p.A79-A89

2006

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Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

Circulation (New York, N.Y.), 2003-05, Vol.107 (17), p.2227-2232

2003

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Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy

Journal of the American College of Cardiology, 2012-07, Vol.60 (2), p.144-156

2012

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Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study

Heart (British Cardiac Society), 2011-01, Vol.97 (2), p.131-136

2011

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A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy

Cardiovascular research, 2009-10, Vol.84 (1), p.83-90

2009

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Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging

European heart journal, 2010-07, Vol.31 (13), p.1599-1607

2010

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Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia

International journal of cardiology, 2012-11, Vol.161 (1), p.50-52

2012

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A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy

European heart journal, 2009-07, Vol.30 (13), p.1648-1655

2009

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Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease

Muscle & nerve, 2006-03, Vol.33 (3), p.393-397

2006

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Are we ready for pharmacogenomics in heart failure?

European Journal of Pharmacology, 2001-04, Vol.417 (1), p.1-9

2001

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Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

Journal of molecular medicine (Berlin, Germany), 1998-03, Vol.76 (3-4), p.208-214

1998

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Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

Journal of medical genetics, 1999-07, Vol.36 (7), p.542-545

1999

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Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy

European heart journal, 2005-09, Vol.26 (18), p.1882-1886

2005

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Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case

Prenatal diagnosis, 2004-09, Vol.24 (9), p.701-703

2004

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Mutational analysis of the β- and δ-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

American journal of medical genetics, 2003-07, Vol.120A (1), p.8-12

2003

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Antibody-mediated vascular rejection of kidney allografts: a population-based study

The Lancet (British edition), 2013, Vol.381 (9863), p.313-319

2013

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Complement-Binding Anti-HLA Antibodies and Kidney-Allograft Survival

The New England journal of medicine, 2013-09, Vol.369 (13), p.1215-1226

2013

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Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy

Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study

The Genetic Bases of Cardiomyopathies

Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy

Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study

A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy

Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging

Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia

A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy

Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease

Are we ready for pharmacogenomics in heart failure?

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy

Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case

Mutational analysis of the β- and δ-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

Antibody-mediated vascular rejection of kidney allografts: a population-based study

Complement-Binding Anti-HLA Antibodies and Kidney-Allograft Survival

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