| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18585512 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 110 journal articles in the PubMed database | Email to a friend | | |
| Parks SB, Kushner JD, Nauman D, et al.
Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. [Journal Article, Research Support, N.I.H., Extramural]
Am Heart J 2008 Jul; 156(1):161-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Taylor MR, Fain PR, Sinagra G, et al.
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. [Journal Article, Multicenter Study]
J Am Coll Cardiol 2003 Mar 5; 41(5):771-80.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Bilińska ZT, Sylvius N, Grzybowski J, et al.
Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies. [JOURNAL ARTICLE]
Kardiol Pol 2006 Aug; 64(8):812-819.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | van Tintelen JP, Hofstra RM, Katerberg H, et al.
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics. [Journal Article]
Am Heart J 2007 Dec; 154(6):1130-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Sébillon P, Bouchier C, Bidot LD, et al.
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations. [Journal Article, Multicenter Study]
J Med Genet 2003 Aug; 40(8):560-7.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Fatkin D, MacRae C, Sasaki T, et al.
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. [Journal Article]
N Engl J Med 1999 Dec 2; 341(23):1715-24.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Hershberger RE, Hanson EL, Jakobs PM, et al.
A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation. [Journal Article]
Am Heart J 2002 Dec; 144(6):1081-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Perrot A, Sigusch HH, Nägele H, et al.
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: Demand for strategies in the management of presymptomatic lamin A/C mutant carriers. [JOURNAL ARTICLE]
Eur J Heart Fail 2005 Dec 28.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Song K, Dube MP, Lim J, et al.
Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in Koreans. [Journal Article]
Exp Mol Med 2007 Feb 28; 39(1):114-20.
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