(Q40499701)

21 September 2017

1 reference

title

Hereditary dilated cardiomyopathy (English)

1 reference

21 September 2017

0 references

McMinn TR Jr

1

1 reference

PubMed ID

7704989

21 September 2017

Ross J Jr

series ordinal

2

1 reference

21 September 2017

1 January 1995

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21 September 2017

1 reference

21 September 2017

18

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21 September 2017

7-15

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21 September 2017

1

1 reference

Dilated cardiomyopathies of the adult (first of two parts).

21 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

The clinical course of idiopathic dilated cardiomyopathy. A population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Idiopathic cardiomyopathy in the United States, 1970-1982.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

The natural history of idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Primary cardiomyopathy in identical twins

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

The epidemiology of idiopathic dilated cardiomyopathy in a biracial community

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial aggregation of idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Clinical and pathologic study of familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Frequency of familial nature of dilated cardiomyopathy and usefulness of cardiac transplantation in this subset

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Clinical and pathologic findings of myocarditis in two families with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A case report of siblings with hypertrophic cardiomyopathy that progressed to dilated cardiomyopathy--case reports

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Dominant and recessive modes of inheritance in idiopathic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Idiopathic familial myocardiopathy in three generations: a clinical and pathologic study

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial cardiomyopathy: Autosomally, dominantiy inherited congestive cardiomyopathy with two cases of septal hypertrophy in one family

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A family with congestive cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Dominantly inherited dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A familial dilated cardiomyopathy associated with cataracts and hip-spine disease

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Dilated cardiomyopathy in identical twins

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

X-linked dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Possible X linked congenital mitochondrial cardiomyopathy in three families

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Mitochondrial mutation in fatal infantile cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Cardiomyopathy with mitochondrial DNA mutations

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Mitochondrial DNA mutations in cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Detection of a specific mitochondrial DNA deletion in tissues of older humans

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Right ventricular dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial right ventricular dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial right ventricular dilated cardiomyopathy associated with supraventricular arrhythmias

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Arrhythmogenic right ventricular dysplasia in a family

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Right ventricular dysplasia: a familial cardiomyopathy?

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial occurrence of right ventricular dysplasia: a study involving nine families

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Right ventricular dysplasia: a clinical and pathological study of two families with left ventricular involvement

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A report of Uhl's disease in identical adult twins: evaluation of right ventricular dysfunction with echocardiography and nuclear angiography.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial Uhl's anomaly in the adult

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial Uhl's anomaly

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transport

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Molecular genetic aspects of cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

The natural history of cardiac involvement in myotonic dystrophy: an eight-year follow-up in 17 patients

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Genetic linkage between the loci for myotonic dystrophy and peptidase D

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Location on chromosome 15 of the gene defect causing Marfan syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

The current status of myocardial disarray in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

The genetics of hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial Prevalence and Genetic Transmission of Idiopathic Hypertrophic Subaortic Stenosis

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Expression of a missense mutation in the messenger RNA for beta-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

No evidence for linkage of familial hypertrophic cardiomyopathy and chromosome 14q1 locus D14S26 in a Chinese family: evidence for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Novel missense mutation in cardiac beta myosin heavy chain gene found in a Japanese patient with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Diagnosis of genetic disorders at the DNA level

1 reference

https://api.crossref.org/works/10.1002%2FCLC.4960180105

7 January 2021

Identifiers

DOI

10.1002/CLC.4960180105

1 reference

21 September 2017

1 reference

PubMed ID

7704989