(Q36627307)

15 August 2017

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7. (English)

1 reference

15 August 2017

K van Engelen

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15 August 2017

A V Postma

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15 August 2017

J B A van de Meerakker

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15 August 2017

J W Roos-Hesselink

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15 August 2017

A T J M Helderman-van den Enden

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15 August 2017

H W Vliegen

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15 August 2017

T Rahman

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15 August 2017

M J H Baars

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15 August 2017

J-W Sels

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15 August 2017

U Bauer

10

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15 August 2017

T Pickardt

11

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15 August 2017

S R Sperling

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15 August 2017

A F M Moorman

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15 August 2017

B Keavney

14

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15 August 2017

J Goodship

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15 August 2017

S Klaassen

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15 August 2017

B J M Mulder

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15 August 2017

1 March 2013

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Netherlands Heart Journal

15 August 2017

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15 August 2017

21

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15 August 2017

3

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15 August 2017

113-117

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https://scigraph.springernature.com/pub.10.1007/s12471-011-0141-1

15 August 2017

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cites work

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

1 reference

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Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Analysis of ventricular hypertrabeculation and noncompaction using genetically engineered mouse models

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Mutations in sarcomere protein genes in left ventricular noncompaction

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

α-cardiac actin mutations produce atrial septal defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

30 September 2017

1 reference

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Clinical features of isolated ventricular noncompaction in adults long-term clinical course, echocardiographic properties, and predictors of left ventricular failure

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Mutation in myosin heavy chain 6 causes atrial septal defect

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Oriented clonal cell growth in the developing mouse myocardium underlies cardiac morphogenesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Morphological aspects of Ebstein's anomaly in adults

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Ebstein's anomaly and extracardiac defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Ebstein's malformation of the tricuspid valve: genetic and environmental factors. The Baltimore-Washington Infant Study Group

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

Noncompacted myocardium in Ebstein's anomaly: initial description in three patients.

28 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0141-1

Familial biventricular myocardial noncompaction associated with Ebstein's malformation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0141-1

Lineage and morphogenetic analysis of the cardiac valves.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0141-1

Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0141-1

Left heart lesions in patients with Ebstein anomaly.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578524

The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction Cardiomyopathy

20 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0141-1

Ebstein Anomaly Associated With Left Ventricular Noncompaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12471-011-0141-1

A rare case of interstitial del(1)(p34.3p36.11) diagnosed prenatally

21 January 2018

1 reference

12 December 2020

Ebstein anomaly and duplication of the distal arm of chromosome 15: report of two patients

1 reference

12 December 2020

Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly

1 reference

12 December 2020

Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis

1 reference

12 December 2020

10.1007/S12471-011-0141-1

Identifiers

DOI

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15 August 2017

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15 August 2017

1 reference