(Q78032668)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

title

Periodic rescreening is indicated for family members at risk of developing familial dilated cardiomyopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

main subject

dilated cardiomyopathy

1 reference

familial dilated cardiomyopathy

inferred from title

1 reference

Kathy A Crispell

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Emily L Hanson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Kelly Coates

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Warren Toy

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Ray E Hershberger

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

language of work or name

English

0 references

publication date

1 May 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

Journal of the American College of Cardiology

10 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

volume

39

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

page(s)

1503-1507

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

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

10 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Molecular genetics of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

High Incidence of Sudden Death with Conduction System and Myocardial Disease Due to Lamins A and C Gene Mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

Genetic Counseling and Screening Issues in Familial Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2802%2901788-6

7 January 2021

10.1016/S0735-1097(02)01788-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11985914%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

1 reference