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Items: 1 to 20 of 36

1.

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.

Hershberger RE, Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Litt M.

Am Heart J. 2002 Dec;144(6):1081-6.

PMID:
12486434
2.

Mutations in the LMNA gene encoding lamin A/C.

Genschel J, Schmidt HH.

Hum Mutat. 2000 Dec;16(6):451-9. Review.

PMID:
11102973
3.

Lamin A/C and cardiac diseases.

Sylvius N, Tesson F.

Curr Opin Cardiol. 2006 May;21(3):159-65. Review.

PMID:
16601451
4.

Lamin A/C deficiency as a cause of familial dilated cardiomyopathy.

Malhotra R, Mason PK.

Curr Opin Cardiol. 2009 May;24(3):203-8. doi: 10.1097/HCO.0b013e32832a11c6. Review.

PMID:
19384091
5.

[Diseases associated with lamin A/C gene defects: what the clinical cardiologist ought to know].

Pasotti M, Repetto A, Pisani A, Arbustini E.

Ital Heart J Suppl. 2004 Feb;5(2):98-111. Review. Italian.

PMID:
15080529
6.

[Genetics of dilated cardiomyopathy].

Osterziel KJ, Scheffold T, Perrot A, Dietz R; Netzwerk Myokardiale Erkrankungen.

Z Kardiol. 2001 Jul;90(7):461-9. Review. German.

PMID:
11515275
7.

The laminopathies: a clinical review.

Rankin J, Ellard S.

Clin Genet. 2006 Oct;70(4):261-74. Review. Erratum in: Clin Genet. 2007 Mar;71(3):293.

PMID:
16965317
8.

Heart involvement in lamin A/C related diseases.

Ben Yaou R, Gueneau L, Demay L, Stora S, Chikhaoui K, Richard P, Bonne G.

Arch Mal Coeur Vaiss. 2006 Sep;99(9):848-55. Review.

PMID:
17067107
9.

[Laminopathies--one gene, multiple diseases].

Song SJ, Zhang YZ, Zhong N.

Beijing Da Xue Xue Bao. 2005 Feb 18;37(1):96-9. Review. Chinese.

10.

[Familial dilated cardiomyopathy].

Osterziel KJ, Hassfeld S, Geier C, Perrot A.

Herz. 2005 Sep;30(6):529-34. Review. German.

PMID:
16170685
11.

Lamin A/C mutations in dilated cardiomyopathy.

Tesson F, Saj M, Uvaize MM, Nicolas H, Płoski R, Bilińska Z.

Cardiol J. 2014;21(4):331-42. doi: 10.5603/CJ.a2014.0037. Epub 2014 May 20. Review.

PMID:
24846508
12.

Arrhythmogenic inherited heart muscle diseases in children.

Towbin JA, Bowles NE.

J Electrocardiol. 2001;34 Suppl:151-65. Review.

PMID:
11781950
13.

[Review: genetics of familial dilated cardiomyopathy].

Amara ME, Villard E, Komajda M.

Ann Cardiol Angeiol (Paris). 2005 Jun;54(3):151-6. Review. French.

PMID:
15991472
14.

Genetics of familial cardiomyopathies and arrhythmias.

Keller DI, Carrier L, Schwartz K.

Swiss Med Wkly. 2002 Jul 27;132(29-30):401-7. Review.

PMID:
12428185
15.

Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.

Kayvanpour E, Sedaghat-Hamedani F, Amr A, Lai A, Haas J, Holzer DB, Frese KS, Keller A, Jensen K, Katus HA, Meder B.

Clin Res Cardiol. 2017 Feb;106(2):127-139. doi: 10.1007/s00392-016-1033-6. Epub 2016 Aug 30. Review.

PMID:
27576561
16.

[Genetic diagnosis of familial dilated cardiomyopathy].

Pasotti M, Repetto A, Pisani A, Arbustini E.

Ital Heart J Suppl. 2002 Apr;3(4):386-93. Review. Italian.

PMID:
12025381
17.

'State-of-the-heart' of cardiac laminopathies.

Cattin ME, Muchir A, Bonne G.

Curr Opin Cardiol. 2013 May;28(3):297-304. doi: 10.1097/HCO.0b013e32835f0c79. Review.

PMID:
23455585
18.

[LMNA gene and dilated cardiomyopathy].

Sun LP, Pu JL.

Zhonghua Xin Xue Guan Bing Za Zhi. 2009 Dec;37(12):1140-2. Review. Chinese. No abstract available.

PMID:
20193191
19.

Advances in molecular genetics of dilated cardiomyopathy. The Heart Muscle Disease Study Group.

Mestroni L, Rocco C, Vatta M, Miocic S, Giacca M.

Cardiol Clin. 1998 Nov;16(4):611-21, vii. Review.

PMID:
9891591
20.

Laminopathies: a Pandora's box of heart failure, bradyarrhythmias and sudden death.

Cabanelas N, Martins VP.

Rev Port Cardiol. 2015 Feb;34(2):139.e1-5. doi: 10.1016/j.repc.2014.08.007. Epub 2015 Feb 3. Review. English, Portuguese.

PMID:
25656816

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