Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected (Q73016833)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

31 October 2019

title

Familial dilated cardiomyopathy: echocardiographic diagnostic criteria for classification of family members as affected (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

31 October 2019

main subject

dilated cardiomyopathy

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familial dilated cardiomyopathy

inferred from title

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Hershberger RE

1

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31 October 2019

Ni H

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

31 October 2019

Crispell KA

series ordinal

3

1 reference

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31 October 2019

publication date

1 September 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

Journal of Cardiac Failure

31 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

31 October 2019

volume

5

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31 October 2019

issue

3

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31 October 2019

page(s)

203-212

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

Epidemiology of heart failure

31 October 2019

cites work

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Familial Dilated Cardiomyopathy: Cardiac Abnormalities Are Common in Asymptomatic Relatives and May Represent Early Disease

1 reference

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7 January 2021

Frequency and Phenotypes of Familial Dilated Cardiomyopathy

1 reference

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7 January 2021

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

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7 January 2021

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

1 reference

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7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

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7 January 2021

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1 reference

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7 January 2021

Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23

1 reference

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7 January 2021

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

1 reference

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7 January 2021

Clinical profiles of four large pedigrees with familial dilated cardiomyopathy: preliminary recommendations for clinical practice

1 reference

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7 January 2021

Left ventricular dilatation and the risk of congestive heart failure in people without myocardial infarction

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7 January 2021

Echocardiographic measurements in normal subjects from infancy to old age.

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7 January 2021

Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop

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7 January 2021

Gender-specific reference M-mode values in adults: population-derived values with consideration of the impact of height

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7 January 2021

Echocardiographic measurements in normal subjects: Evaluation of an adult population without clinically apparent heart disease

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7 January 2021

The impact of obesity on left ventricular mass and geometry. The Framingham Heart Study

1 reference

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7 January 2021

Familial dilated cardiomyopathy

1 reference

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7 January 2021

10.1016/S1071-9164(99)95005-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10496193 AND SRC:MED&resulttype=core&format=json

31 October 2019

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