Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected.

Journal of cardiac failure - 1 Sept 1999

Hershberger R E, Ni H, Crispell K A

Abstract excerpt

BACKGROUND: Echocardiographic criteria for left ventricular enlargement (LVE) used to classify subjects as affected in families with familial dilated cardiomyopathy (FDC) have been inconsistent. A recent report from a large Framingham echocardiographic study provides an opportunity to improve the assignment of LVE and FDC in kindreds, principally with a dilated phenotype. The objective of this study is to...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiomyopathy, Dilated
Share to Child, Preschool
Share to Echocardiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Heart Ventricles

Share to Infant

Share to Pedigree

Share to Prognosis

Source

Identifiers

PMID: 10496193
DOI: 10.1016/s1071-9164(99)90005-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected.PMID 10496193Read ↗

Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice.Semantic proximity Read ↗

Cardiomyopathy, familial dilatedSemantic proximity Read ↗

Clinical care of family members of patients with dilated cardiomyopathySemantic proximity Read ↗

Familial dilated cardiomyopathy.Semantic proximity Read ↗

Familial risk of dilated and hypertrophic cardiomyopathy: a national family study in Sweden.Semantic proximity Read ↗

Familial dilated cardiomyopathy in the United Kingdom.Semantic proximity Read ↗

Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group.Semantic proximity Read ↗

Frequency and phenotypes of familial dilated cardiomyopathy.Semantic proximity Read ↗

Cardiac manifestations of Fabry disease: are women getting enough attention?Semantic proximity Read ↗

Periodic rescreening is indicated for family members at risk of developing familial dilated cardiomyopathy.Semantic proximity Read ↗

Genetic analysis and family screening for dilated cardiomyopathy: a retrospective analysis of the stepwise pedigree approach.Semantic proximity Read ↗

Severe dilated cardiomyopathy and quadriceps myopathy due to lamin A/C gene mutation: a phenotypic study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.