(Q39506391)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

Familial dilated cardiomyopathy. Clinical and genetic characteristics (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

4

1 reference

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20 February 2020

Eloisa Arbustini

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Alessandra Serio

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

author name string

N Narula

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

T Kodama

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

publication date

1 December 2012

1 reference

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20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

volume

37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

issue

8

1 reference

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20 February 2020

page(s)

822-829

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

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

20 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Where genome meets phenome: rationale for integrating genetic and protein biomarkers in the diagnosis and management of dilated cardiomyopathy and heart failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Frequency and phenotypes of familial dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Frequency of development of idiopathic dilated cardiomyopathy among relatives of patients with idiopathic dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Next-generation sequencing to identify genetic causes of cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Sudden death in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Familial dilated cardiomyopathy: from clinical presentation to molecular genetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Barth syndrome associated with compound hemizygosity and heterozygosity of the TAZ and LDB3 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Genetics and metabolic cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Noncompaction of the left ventricle: primary cardiomyopathy with an elusive genetic etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Genetics of idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Dominant missense mutations in ABCC9 cause Cantú syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Truncations of titin causing dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Genetic testing for dilated cardiomyopathy in clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Profiling of short RNAs using Helicos single-molecule sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Return of genetic results in the familial dilated cardiomyopathy research project

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Alpha B-crystallin mutation in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3707-9

Ventricular dysfunction in type 1 myotonic dystrophy: electrical, mechanical, or both?

21 January 2018

1 reference

12 December 2020

Natural history and familial characteristics of isolated left ventricular non-compaction

1 reference

12 December 2020

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

1 reference

12 December 2020

Dilated Cardiomyopathy in Friedreich's Ataxia: 2D Echo and Tissue-Doppler Analysis of Left Ventricular and Atrial Function

1 reference

12 December 2020

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

1 reference

12 December 2020

Cardiac troponin T mutations promote life-threatening arrhythmias

1 reference

12 December 2020

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

1 reference

12 December 2020

Cardiovascular causes of sudden death in young individuals including athletes

1 reference

12 December 2020

Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy.

1 reference

12 December 2020

Re-examination of the electrocardiogram in boys with Duchenne muscular dystrophy and correlation with its dilated cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Mitochondrial DNA related cardiomyopathies

1 reference

12 December 2020

10.1007/S00059-012-3707-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23223770%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference