(Q41972456)

14 October 2017

0 references

Lamin A/C gene and the heart: how genetics may impact clinical care (English)

1 reference

14 October 2017

Luisa Mestroni

1

0 references

author name string

Matthew R G Taylor

series ordinal

2

1 reference

PMC publication ID

2571955

14 October 2017

language of work or name

English

0 references

publication date

1 October 2008

1 reference

Journal of the American College of Cardiology

14 October 2017

1 reference

14 October 2017

52

1 reference

14 October 2017

15

1 reference

14 October 2017

1261-1262

1 reference

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

14 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

Human laminopathies: nuclei gone genetically awry

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

The laminopathies: a clinical review

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

Novel mutations in the lamin A/C gene in heart transplant recipients with end stage dilated cardiomyopathy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Update the [...]

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

Primary prevention of sudden death in patients with lamin A/C gene mutations.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

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

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

2 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2571955

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

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18926330

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18926330

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JACC.2008.07.021

1 reference

14 October 2017

1 reference

PMC publication ID

2571955

14 October 2017

PubMed publication ID

18926330

1 reference

PMC publication ID

2571955