PubMed (cited) for id: 115200

Year	Number of Results
1949	1
1961	3
1962	2
1964	1
1965	1
1966	1
1969	1
1970	1
1971	2
1979	1
1984	2
1986	1
1987	3
1988	2
1990	1
1992	1
1993	1
1994	1
1995	2
1996	1
1997	1
1999	2
2000	1
2001	1
2003	4
2005	1
2006	1
2010	2
2011	1
2019	1
2024	0

1

Activation of PDGF pathway links LMNA mutation to dilated cardiomyopathy.

Lee J, Termglinchan V, Diecke S, Itzhaki I, Lam CK, Garg P, Lau E, Greenhaw M, Seeger T, Wu H, Zhang JZ, Chen X, Gil IP, Ameen M, Sallam K, Rhee JW, Churko JM, Chaudhary R, Chour T, Wang PJ, Snyder MP, Chang HY, Karakikes I, Wu JC. Lee J, et al. Nature. 2019 Aug;572(7769):335-340. doi: 10.1038/s41586-019-1406-x. Epub 2019 Jul 17. Nature. 2019. PMID: 31316208 Free PMC article.

2

Contribution of genetic factors to the pathogenesis of dilated cardiomyopathy: the cause of dilated cardiomyopathy: genetic or acquired? (genetic-side).

Kimura A. Kimura A. Circ J. 2011;75(7):1756-65; discussion 1765. doi: 10.1253/circj.cj-11-0368. Epub 2011 May 27. Circ J. 2011. PMID: 21617319 Free article. Review.

3

Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase.

Levitas A, Muhammad E, Harel G, Saada A, Caspi VC, Manor E, Beck JC, Sheffield V, Parvari R. Levitas A, et al. Eur J Hum Genet. 2010 Oct;18(10):1160-5. doi: 10.1038/ejhg.2010.83. Epub 2010 Jun 16. Eur J Hum Genet. 2010. PMID: 20551992 Free PMC article.

4

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.

Gupta P, Bilinska ZT, Sylvius N, Boudreau E, Veinot JP, Labib S, Bolongo PM, Hamza A, Jackson T, Ploski R, Walski M, Grzybowski J, Walczak E, Religa G, Fidzianska A, Tesson F. Gupta P, et al. Basic Res Cardiol. 2010 May;105(3):365-77. doi: 10.1007/s00395-010-0085-4. Epub 2010 Feb 3. Basic Res Cardiol. 2010. PMID: 20127487 Free PMC article.

5

Familial cardiomegaly.

EVANS W. EVANS W. Br Heart J. 1949 Jan;11(1):68-82. doi: 10.1136/hrt.11.1.68. Br Heart J. 1949. PMID: 18113470 Free PMC article. No abstract available.

6

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

Meune C, Van Berlo JH, Anselme F, Bonne G, Pinto YM, Duboc D. Meune C, et al. N Engl J Med. 2006 Jan 12;354(2):209-10. doi: 10.1056/NEJMc052632. N Engl J Med. 2006. PMID: 16407522 No abstract available.

7

Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.

Mounkes LC, Kozlov SV, Rottman JN, Stewart CL. Mounkes LC, et al. Hum Mol Genet. 2005 Aug 1;14(15):2167-80. doi: 10.1093/hmg/ddi221. Epub 2005 Jun 22. Hum Mol Genet. 2005. PMID: 15972724

8

Autoimmune cardiomyopathy and heart block develop spontaneously in HLA-DQ8 transgenic IAbeta knockout NOD mice.

Elliott JF, Liu J, Yuan ZN, Bautista-Lopez N, Wallbank SL, Suzuki K, Rayner D, Nation P, Robertson MA, Liu G, Kavanagh KM. Elliott JF, et al. Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13447-52. doi: 10.1073/pnas.2235552100. Epub 2003 Oct 21. Proc Natl Acad Sci U S A. 2003. PMID: 14570980 Free PMC article.

9

THREE FAMILIES WITH FAMILIAL CARDIOMYOPATHY.

BOYD DL, MISKHIN ME, FEIGENBAUM, GENOVES PD. BOYD DL, et al. Ann Intern Med. 1965 Sep;63:386-401. doi: 10.7326/0003-4819-63-3-386. Ann Intern Med. 1965. PMID: 14327505 No abstract available.

10

FAMILIAL CARDIOMYOPATHIES.

BIOERCK G, ORINIUS E. BIOERCK G, et al. Acta Med Scand. 1964 Oct;176:407-24. Acta Med Scand. 1964. PMID: 14221653 No abstract available.

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