doi: 10.1056/NEJMc052632.
Primary prevention of sudden death in patients with lamin A/C gene mutations
- PMID: 16407522
- DOI: 10.1056/NEJMc052632
Item in Clipboard
Primary prevention of sudden death in patients with lamin A/C gene mutations
N Engl J Med.
.
No abstract available
Similar articles
-
Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function.Int J Cardiol. 2008 May 7;126(1):136-7. doi: 10.1016/j.ijcard.2007.01.072. Epub 2007 Apr 17. Int J Cardiol. 2008. PMID: 17442430
-
Expanding the phenotype of sudden cardiac death-An unusual presentation of a family with a Lamin A/C mutation.Int J Cardiol. 2010 Jan 7;138(1):97-9. doi: 10.1016/j.ijcard.2008.06.008. Epub 2008 Aug 8. Int J Cardiol. 2010. PMID: 18691775
-
Lamin A/C mutation: An easily missed opportunity.Int J Cardiol. 2015 Feb 15;181:48-9. doi: 10.1016/j.ijcard.2014.12.013. Epub 2014 Dec 3. Int J Cardiol. 2015. PMID: 25481314 No abstract available.
-
Implantable cardioverter-defibrillators after myocardial infarction.N Engl J Med. 2008 Nov 20;359(21):2245-53. doi: 10.1056/NEJMra0803409. N Engl J Med. 2008. PMID: 19020326 Review. No abstract available.
-
[Implantable cardioverter-defibrillator: prevention of sudden cardiac death and impact on survival in patients with malignant ventricular arrhythmias].Cardiologia. 1995 Jun;40(6):419-25. Cardiologia. 1995. PMID: 8640855 Review. Italian. No abstract available.
Cited by
-
Advances in basic and clinical research in laminopathies.Acta Myol. 2013 May;32(1):18-22. Acta Myol. 2013. PMID: 23853505 Free PMC article. Review.
-
[Genetic testing in hereditary arrythmia syndromes today and in the future].Herzschrittmacherther Elektrophysiol. 2012 Sep;23(3):161-6. doi: 10.1007/s00399-012-0230-x. Epub 2012 Sep 20. Herzschrittmacherther Elektrophysiol. 2012. PMID: 22993117 German.
-
Cardiovascular Involvement in Pediatric Laminopathies. Report of Six Patients and Literature Revision.Front Pediatr. 2020 Jul 24;8:374. doi: 10.3389/fped.2020.00374. eCollection 2020. Front Pediatr. 2020. PMID: 32793522 Free PMC article.
-
Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype.J Huazhong Univ Sci Technolog Med Sci. 2010 Feb;30(1):103-7. doi: 10.1007/s11596-010-0119-z. Epub 2010 Feb 14. J Huazhong Univ Sci Technolog Med Sci. 2010. PMID: 20155465
-
Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene.Biochim Biophys Acta. 2010 Jul-Aug;1802(7-8):632-8. doi: 10.1016/j.bbadis.2010.04.001. Epub 2010 Apr 11. Biochim Biophys Acta. 2010. PMID: 20388542 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
