Similar articles for PMID: 16650083

Year	Number of Results
1978	1
1980	3
1981	8
1983	1
1984	2
1985	1
1986	2
1987	2
1988	1
1989	1
1992	2
1993	2
1994	2
1995	4
1996	5
1997	3
1998	6
1999	7
2000	7
2001	6
2002	5
2003	7
2004	10
2005	13
2006	13
2007	16
2008	13
2009	12
2010	8
2011	13
2012	4
2013	9
2014	10
2015	12
2016	6
2017	10
2018	13
2019	12
2020	7
2021	8
2022	11
2023	2
2024	0

1

Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy.

Tanjore RR, Sikindlapuram AD, Calambur N, Thakkar B, Kerkar PG, Nallari P. Tanjore RR, et al. Clin Genet. 2006 May;69(5):434-6. doi: 10.1111/j.1399-0004.2006.00599.x. Clin Genet. 2006. PMID: 16650083 No abstract available.

2

[Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].

Mora R, Merino JL, Peinado R, Olias F, García-Guereta L, del Cerro MJ, Tarín MN, Molano J. Mora R, et al. Rev Esp Cardiol. 2006 Aug;59(8):846-9. Rev Esp Cardiol. 2006. PMID: 16938236 Free article. Spanish.

3

Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.

Overeem S, Schelhaas HJ, Blijham PJ, Grootscholten MI, ter Laak HJ, Timmermans J, van den Wijngaard A, Zwarts MJ. Overeem S, et al. Neuromuscul Disord. 2007 Jun;17(6):490-3. doi: 10.1016/j.nmd.2007.02.007. Epub 2007 Mar 23. Neuromuscul Disord. 2007. PMID: 17383184

4

Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.

Tesson F, Richard P, Charron P, Mathieu B, Cruaud C, Carrier L, Dubourg O, Lautié N, Desnos M, Millaire A, Isnard R, Hagege AA, Bouhour JB, Bennaceur M, Hainque B, Guicheney P, Schwartz K, Komajda M. Tesson F, et al. Hum Mutat. 1998;12(6):385-92. doi: 10.1002/(SICI)1098-1004(1998)12:6<385::AID-HUMU4>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9829907

5

Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives.

Maron BJ, Maron MS, Semsarian C. Maron BJ, et al. J Am Coll Cardiol. 2012 Aug 21;60(8):705-15. doi: 10.1016/j.jacc.2012.02.068. Epub 2012 Jul 11. J Am Coll Cardiol. 2012. PMID: 22796258 Free article. Review.

6

Gene symbol: MYH7. Disease: cardiomyopathy, hypertrophic.

Capek PC. Capek PC. Hum Genet. 2005 Dec;118(3-4):537. Hum Genet. 2005. PMID: 16521248 No abstract available.

7

[The Val606Met mutation of human beta myosin heavy chain in a Chinese familial hypertrophic cardiomyopathy family].

Yuan JS, Qiao SB, Wang SX, Teng SY, You SJ, Yang WX, Gao RL, Chen JL, Yang YJ. Yuan JS, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2008 Apr;36(4):313-6. Zhonghua Xin Xue Guan Bing Za Zhi. 2008. PMID: 19100006 Chinese.

8

[Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families].

Fan XP, Yang ZW, Feng XL, Yang FH, Xiao B, Liang Y. Fan XP, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):387-92. doi: 10.3760/cma.j.issn.1003-9406.2011.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811976 Chinese.

9

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.

Bundgaard H, Havndrup O, Andersen PS, Larsen LA, Brandt NJ, Vuust J, Kjeldsen K, Christiansen M. Bundgaard H, et al. J Mol Cell Cardiol. 1999 Apr;31(4):745-50. doi: 10.1006/jmcc.1998.0911. J Mol Cell Cardiol. 1999. PMID: 10329202

10

A novel de novo mutation of β-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy.

Okada S, Suzuki Y, Arimura T, Kimura A, Narumi H, Hasegawa S. Okada S, et al. J Genet. 2014 Aug;93(2):557-60. doi: 10.1007/s12041-014-0414-8. J Genet. 2014. PMID: 25189259 Free article. No abstract available.

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