Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases (Q37786123)

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scientific article published on 07 September 2010

Language	Label	Description	Also known as
English	Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases	scientific article published on 07 September 2010

Statements

scholarly article

1 reference

Europe PubMed Central

23 August 2017

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

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Europe PubMed Central

23 August 2017

William McKenna

9

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Europe PubMed Central

23 August 2017

Philippe Charron

object named as

Philippe Charron

1

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Zofia Bilińska

object named as

Zofia Bilinska

5

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Lorenzo Monserrat

object named as

Lorenzo Monserrat

10

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Claudio Rapezzi

object named as

Claudio Rapezzi

13

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Eloisa Arbustini

object named as

Eloisa Arbustini

3

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17

object named as

Luigi Tavazzi

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Europe PubMed Central

23 August 2017

author name string

Michael Arad

2

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Europe PubMed Central

23 August 2017

Cristina Basso

4

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Europe PubMed Central

23 August 2017

Perry Elliott

6

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Europe PubMed Central

23 August 2017

Tiina Helio

7

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Europe PubMed Central

23 August 2017

Andre Keren

8

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Europe PubMed Central

23 August 2017

Sabine Pankuweit

11

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Europe PubMed Central

23 August 2017

Andreas Perrot

12

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Europe PubMed Central

23 August 2017

Arsen Ristic

14

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Europe PubMed Central

23 August 2017

Hubert Seggewiss

15

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Europe PubMed Central

23 August 2017

Irene van Langen

16

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Europe PubMed Central

23 August 2017

European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

18

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Europe PubMed Central

23 August 2017

language of work or name

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based on heuristic

inferred from title

publication date

7 September 2010

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Europe PubMed Central

23 August 2017

European Heart Journal

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Europe PubMed Central

23 August 2017

31

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Europe PubMed Central

23 August 2017

22

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Europe PubMed Central

23 August 2017

2715-2726

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Europe PubMed Central

23 August 2017

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Clinical and genetic issues in familial dilated cardiomyopathy

1 reference

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21 January 2018

New insights into the pathology of inherited cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Genetic testing in cardiovascular disease

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy

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21 January 2018

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

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21 January 2018

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

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21 January 2018

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

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21 January 2018

Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations

1 reference

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21 January 2018

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Different presentation of hypertrophic cardiomyopathy in monozygotic twins

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Arrhythmogenic right ventricular cardiomyopathy in two pairs of monozygotic twins.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Genetic determinants of cardiac hypertrophy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure

1 reference

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21 January 2018

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

1 reference

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21 January 2018

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

1 reference

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21 January 2018

ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Update the [...]

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21 January 2018

Recommendations for competitive sports participation in athletes with cardiovascular disease: a consensus document from the Study Group of Sports Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group

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21 January 2018

Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases.

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21 January 2018

Risk associated with pregnancy in hypertrophic cardiomyopathy

1 reference

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21 January 2018

Pregnancy in women with arrhythmogenic right ventricular cardiomyopathy/dysplasia.

1 reference

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21 January 2018

Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy

1 reference

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21 January 2018

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International S

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Primary prevention of sudden death in patients with lamin A/C gene mutations.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Clinical outcome and phenotypic expression in LAMP2 cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene.

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history

1 reference

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21 January 2018

Athlete's heart or hypertrophic cardiomyopathy?

1 reference

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21 January 2018

Guidelines for autopsy investigation of sudden cardiac death

1 reference

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21 January 2018

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience

1 reference

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21 January 2018

Genetic testing for familial hypertrophic cardiomyopathy in newborn infants

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https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHQ271

21 January 2018

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

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21 January 2018

Psychological consequences of predictive genetic testing: a systematic review

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The psychological complexity of predictive testing for late onset neurogenetic diseases and hereditary cancers: implications for multidisciplinary counselling and for genetic education.

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Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: a cross-sectional cohort study.

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21 January 2018

Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations

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Testing the children: do non-genetic health-care providers differ in their decision to advise genetic presymptomatic testing on minors? A cross-sectional study in five countries in the European Union.

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Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research

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Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

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Genomic medicine in prenatal diagnosis

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Preimplantation genetic diagnosis: technological advances to improve accuracy and range of applications

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What do we mean by genetic testing?

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Genetic diagnosis and testing in clinical practice

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Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

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Mutations in sarcomere protein genes in left ventricular noncompaction

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Comparison of genetic services with and without genetic registers: knowledge, adjustment, and attitudes about genetic counselling among probands referred to three genetic clinics

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The role and practice of the genetic nurse: report of the AGNC Working Party

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Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey

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Extreme phenotypic diversity and nonpenetrance in families with theLMNA gene mutation R644C

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Predictive genetic testing for cardiovascular diseases: Impact on carrier children

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

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Identifiers

10.1093/EURHEARTJ/EHQ271

1 reference

Europe PubMed Central

23 August 2017

1 reference

Europe PubMed Central

23 August 2017

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