(Q37067665)

18 August 2017

1 reference

title

The genetics of cardiomyopathies: what clinicians should know (English)

1 reference

18 August 2017

Rahul Deo

1

1 reference

18 August 2017

Calum A MacRae

series ordinal

2

1 reference

18 August 2017

publication date

1 December 2007

1 reference

Current heart failure reports

18 August 2017

published in

1 reference

18 August 2017

volume

4

1 reference

18 August 2017

issue

4

1 reference

18 August 2017

page(s)

229-235

1 reference

Idiopathic dilated cardiomyopathy: familial prevalence and HLA distribution

18 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11897-007-0017-2

Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11897-007-0017-2

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11897-007-0017-2

Predictors of appropriate implantable defibrillator therapies in patients with arrhythmogenic right ventricular dysplasia.

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

1 reference

12 December 2020

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

12 December 2020

Familial restrictive cardiomyopathy with atrioventricular block and skeletal myopathy

1 reference

12 December 2020

Spectrum of ALMS1 variants and evaluation of genotype-phenotype correlations in Alström syndrome

1 reference

12 December 2020

Arrhythmogenic right-ventricular dysplasia/cardiomyopathy

1 reference

12 December 2020

Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital.

1 reference

12 December 2020

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

1 reference

12 December 2020

Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy

1 reference

12 December 2020

Morphologic spectrum of primary restrictive cardiomyopathy

1 reference

12 December 2020

A contemporary approach to hypertrophic cardiomyopathy.

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?

1 reference

12 December 2020

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

12 December 2020

Serial reevaluation for ARVD/C is indicated in patients presenting with left bundle branch block ventricular tachycardia and minor ECG abnormalities.

1 reference

12 December 2020

Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria

1 reference

12 December 2020

Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.

1 reference

12 December 2020

Arrhythmogenic right ventricular dysplasia: a United States experience

1 reference

12 December 2020

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 2001 G

1 reference

12 December 2020

The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)

1 reference

12 December 2020

Evidence for microvascular dysfunction in hypertrophic cardiomyopathy: new insights from multiparametric magnetic resonance imaging

1 reference

12 December 2020

Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

1 reference

12 December 2020

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

1 reference

12 December 2020

Sudden death due to troponin T mutations

1 reference

12 December 2020

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective

1 reference

12 December 2020

Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance.

1 reference

12 December 2020

Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy.

1 reference

12 December 2020

Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.

1 reference

12 December 2020

Prevalence of hypertrophic cardiomyopathy in a population-based sample of American Indians aged 51 to 77 years (the Strong Heart Study)

1 reference

12 December 2020

Sudden death in hypertrophic cardiomyopathy: identification of high risk patients.

1 reference

12 December 2020

Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype

1 reference

12 December 2020

Late-onset arrhythmogenic right ventricular cardiomyopathy.

1 reference

12 December 2020

Prevalence of Desmin Mutations in Dilated Cardiomyopathy

1 reference

12 December 2020

Implantable cardioverter-defibrillator therapy in arrhythmogenic right ventricular cardiomyopathy: a role for genotyping in decision-making?

1 reference

12 December 2020

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

1 reference

12 December 2020

Clinical course of hypertrophic cardiomyopathy in a regional United States cohort

1 reference

12 December 2020

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

1 reference

12 December 2020

New insights into the pathology of inherited cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Survival after cardiac arrest or sustained ventricular tachycardia in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of left ventricular diastolic function by tissue Doppler imaging and clinical status in children with hypertrophic cardiomyopathy

1 reference

12 December 2020

Functional and histopathologic correlation in patients with dilated cardiomyopathy: an integrated evaluation by multivariate analysis.

1 reference

12 December 2020

Predictors of adverse outcome in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy: long term experience of a tertiary care centre.

1 reference

12 December 2020

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

1 reference

12 December 2020

The Genetic Basis for Cardiomyopathy

1 reference

12 December 2020

10.1007/S11897-007-0017-2

Identifiers

DOI

1 reference

18 August 2017

1 reference