Genetics of inherited cardiomyopathy. (Q35721684)

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9 February 2020

review article

1 reference

title

Genetics of inherited cardiomyopathy (English)

1 reference

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9 February 2020

2

1 reference

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9 February 2020

author name string

Daniel Jacoby

series ordinal

1

1 reference

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9 February 2020

publication date

2 August 2011

1 reference

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9 February 2020

published in

European Heart Journal

1 reference

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9 February 2020

volume

33

1 reference

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9 February 2020

issue

3

1 reference

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9 February 2020

page(s)

296-304

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Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy

9 February 2020

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Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing?

12 July 2018

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The pediatric cardiomyopathy registry and heart failure: key results from the first 15 years

12 July 2018

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Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals

12 July 2018

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The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease.

12 July 2018

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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

12 July 2018

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Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier.

12 July 2018

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Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy.

12 July 2018

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Exercise prescription and primary prevention of cardiovascular disease

12 July 2018

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Emotional stress triggers symptoms in hypertrophic cardiomyopathy: a survey of the Hypertrophic Cardiomyopathy Association

12 July 2018

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Narrative review: harnessing molecular genetics for the diagnosis and management of hypertrophic cardiomyopathy

12 July 2018

1 reference

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Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy

12 July 2018

1 reference

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Genetics of restrictive cardiomyopathy

12 July 2018

1 reference

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DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model

12 July 2018

1 reference

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12 July 2018

Dilated cardiomyopathy

1 reference

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Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria

12 July 2018

1 reference

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Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy

12 July 2018

1 reference

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Defining and setting national goals for cardiovascular health promotion and disease reduction: the American Heart Association's strategic Impact Goal through 2020 and beyond

12 July 2018

1 reference

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Arrhythmogenic cardiomyopathy: etiology, diagnosis, and treatment

12 July 2018

1 reference

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Left ventricular non-compaction: genetic heterogeneity, diagnosis and clinical course

12 July 2018

1 reference

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Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy

12 July 2018

1 reference

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Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy

12 July 2018

1 reference

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A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy

12 July 2018

1 reference

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Left ventricular noncompaction

12 July 2018

1 reference

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Sudden deaths in young competitive athletes: analysis of 1866 deaths in the United States, 1980-2006.

12 July 2018

1 reference

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The effects of candesartan on left ventricular hypertrophy and function in nonobstructive hypertrophic cardiomyopathy: a pilot, randomized study

12 July 2018

1 reference

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Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

12 July 2018

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The Ser96Ala variant in histidine-rich calcium-binding protein is associated with life-threatening ventricular arrhythmias in idiopathic dilated cardiomyopathy

12 July 2018

1 reference

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

12 July 2018

1 reference

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Mutations in sarcomere protein genes in left ventricular noncompaction

12 July 2018

1 reference

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Genetic analysis of the Irx4 gene in hypertrophic cardiomyopathy

12 July 2018

1 reference

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Identifying modifier loci in existing genome scan data

12 July 2018

1 reference

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Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

12 July 2018

1 reference

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Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

12 July 2018

1 reference

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Prevalence and characteristics of left ventricular noncompaction in a community hospital cohort of patients with systolic dysfunction

12 July 2018

1 reference

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Diagnosis of left-ventricular non-compaction in patients with left-ventricular systolic dysfunction: time for a reappraisal of diagnostic criteria?

12 July 2018

1 reference

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Calcium cycling and signaling in cardiac myocytes.

12 July 2018

1 reference

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Phenotypic plasticity of sarcomeric protein mutations

12 July 2018

1 reference

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Exercise reverses preamyloid oligomer and prolongs survival in alphaB-crystallin-based desmin-related cardiomyopathy

12 July 2018

1 reference

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Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

12 July 2018

1 reference

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Clinical features of isolated ventricular noncompaction in adults long-term clinical course, echocardiographic properties, and predictors of left ventricular failure

12 July 2018

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Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction

12 July 2018

1 reference

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Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

12 July 2018

1 reference

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The laminopathies: a clinical review

12 July 2018

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A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation.

12 July 2018

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Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy

12 July 2018

1 reference

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Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.

12 July 2018

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12 July 2018

1 reference

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Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

12 July 2018

1 reference

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A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria.

12 July 2018

1 reference

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Sarcomeric protein mutations in dilated cardiomyopathy

12 July 2018

1 reference

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

12 July 2018

1 reference

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Arrhythmogenic right ventricular dysplasia: a United States experience

12 July 2018

1 reference

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The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient

12 July 2018

1 reference

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The genetic basis for cardiac remodeling

12 July 2018

1 reference

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Genetics of right ventricular cardiomyopathy

12 July 2018

1 reference

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Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy

12 July 2018

1 reference

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

12 July 2018

1 reference

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Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development

12 July 2018

1 reference

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

12 July 2018

1 reference

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Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

12 July 2018

1 reference

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Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

12 July 2018

1 reference

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Desmin: a major intermediate filament protein essential for the structural integrity and function of muscle

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

12 July 2018

1 reference

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12 July 2018

1 reference

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Naxos disease and Carvajal syndrome: cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro

12 July 2018

1 reference

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Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

12 July 2018

1 reference

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Maximum left ventricular thickness and risk of sudden death in patients with hypertrophic cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model

12 July 2018

1 reference

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Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

R403Q and L908V mutant beta-cardiac myosin from patients with familial hypertrophic cardiomyopathy exhibit enhanced mechanical performance at the single molecule level

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Hypertrophic cardiomyopathy: the interrelation of disarray, fibrosis, and small vessel disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Cardiovascular causes of sudden death in young individuals including athletes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

A novel X-linked gene, G4.5. is responsible for Barth syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Prevalence of hypertrophic cardiomyopathy in an outpatient population referred for echocardiographic study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Relation of Left Ventricular Mass and Geometry to Morbidity and Mortality in Uncomplicated Essential Hypertension

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Effect of enalapril on mortality and the development of heart failure in asymptomatic patients with reduced left ventricular ejection fractions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Use of mouse models to evaluate novel therapeutic approaches to treatment of arrhythmogenic right ventricular cardiomyopathy the future is now.

12 July 2018

1 reference

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Metabolic modulator perhexiline corrects energy deficiency and improves exercise capacity in symptomatic hypertrophic cardiomyopathy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Pharmacogenetic interactions between Angiotensin-converting enzyme insertion/deletion polymorphism and response to cibenzoline in patients with hypertrophic obstructive cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Reversible phenotype in a mouse model of Hutchinson-Gilford progeria syndrome

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Dilated cardiomyopathy and sudden death in a teenager with palmar-plantar keratosis (occult Carvajal syndrome).

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Yield of genetic testing in hypertrophic cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Association of beta-adrenergic receptor polymorphisms and progression to heart failure in patients with idiopathic dilated cardiomyopathy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Does sports activity enhance the risk of sudden death in adolescents and young adults?

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Clinical profile and outcome of idiopathic restrictive cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Increased left ventricular mass and hypertrophy are associated with increased risk for sudden death

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Frequency and phenotypes of familial dilated cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Response to Letter Regarding Article, “Hypertrophic Cardiomyopathy Is Predominantly a Disease of Left Ventricular Outflow Tract Obstruction”

23 October 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

Familial Evaluation in Arrhythmogenic Right Ventricular Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

Mutational Heterogeneity, Modifier Genes, and Environmental Influences Contribute to Phenotypic Diversity of Arrhythmogenic Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

Small changes in expression affect predisposition to tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

The intercalated disk as a single functional unit

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHR260

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3270042

Psychological issues in genetic testing for inherited cardiovascular diseases

7 December 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Familial hypertrophic cardiomyopathy mutations from different functional regions of troponin T result in different effects on the pH and Ca2+ sensitivity of cardiac muscle contraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Mechanism of left ventricular outlfow obstruction in patients with obstructive asymmetric septal hypertrophy (idiopathic hypertrophic subaortic stenosis)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

An X-linked recessive cardiomyopathy with abnormal mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Glycogen storage disease confined to the heart with deficient activity of cardiac phosphorylase kinase: a new type of glycogen storage disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy: an update

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Tropomyosin and dilated cardiomyopathy: revenge of the actinomyosin "gatekeeper"

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Arrhythmogenic right ventricular dysplasia masquerading as peripartum cardiomyopathy with atrial flutter, advanced atrioventricular block and embolic stroke

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Restrictive left ventricular filling pattern in dilated cardiomyopathy assessed by Doppler echocardiography: clinical, echocardiographic and hemodynamic correlations and prognostic implications. Heart Muscle Disease Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Papillary muscle displacement causes systolic anterior motion of the mitral valve. Experimental validation and insights into the mechanism of subaortic obstruction

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Pathology of arrhythmogenic right ventricular cardiomyopathy/dysplasia--an autopsy study of 20 forensic cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Long-term outcome and prognostic determinants in children with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

The pathogenesis of familial hypertrophic cardiomyopathy: early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Familial dilated cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Arrhythmogenic right ventricular dysplasia masquerading as dilated cardiomyopathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Circumstances of death and gross and microscopic observations in a series of 200 cases of sudden death associated with arrhythmogenic right ventricular cardiomyopathy and/or dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Alterations of tension-dependent ATP utilization in a transgenic rat model of hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Prospective familial assessment in dilated cardiomyopathy: cardiac autoantibodies predict disease development in asymptomatic relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Prevalence of Desmin Mutations in Dilated Cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Letter by Geier et al regarding article, "Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction"

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Arrhythmogenic right ventricular dysplasia masquerading as dilated cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21810862

12 December 2020

Identifiers

DOI

10.1093/EURHEARTJ/EHR260

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21810862%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21810862%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

PubMed publication ID

21810862

1 reference