Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 112

1.

Familial restrictive cardiomyopathy with 12 affected family members.

Daneshvar DA, Kedia G, Fishbein MC, Siegel RJ.

Am J Cardiol. 2012 Feb 1;109(3):445-7. doi: 10.1016/j.amjcard.2011.09.031. Epub 2011 Nov 8. No abstract available.

PMID:
22071211
[PubMed - indexed for MEDLINE]
2.

Genetic evaluation of familial cardiomyopathy.

Judge DP, Johnson NM.

J Cardiovasc Transl Res. 2008 Jun;1(2):144-54. doi: 10.1007/s12265-008-9025-1. Epub 2008 Apr 22. Review.

PMID:
20559909
[PubMed - indexed for MEDLINE]
3.

Familial restrictive cardiomyopathy with skeletal abnormalities.

Schwartz ML, Colan SD.

Am J Cardiol. 2003 Sep 1;92(5):636-9.

PMID:
12943897
[PubMed - indexed for MEDLINE]
4.

A novel mutation of the beta myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.

Wang J, Xu SJ, Zhou H, Wang LJ, Hu B, Fang F, Zhang XM, Luo YW, He XY, Zhuang SW, Li XM, Liu ZM, Hu DY.

Clin Cardiol. 2009 Sep;32(9):E16-21. doi: 10.1002/clc.20520.

PMID:
19645038
[PubMed - indexed for MEDLINE]
5.

[Familial hypertrophic cardiomyopathy--a case report].

Domal-Kwiatkowska D, Glanowska G, Smolik S, Wilczewski P, Mazurek U, Nowalany-Kozielska E, Fudal M, Wodniecki J.

Kardiol Pol. 2006 Nov;64(11):1287-91. Polish.

PMID:
17165166
[PubMed - indexed for MEDLINE]
6.

Familial conduction system disease associated with hypertrophic cardiomyopathy.

Bahl A, Saikia UN, Talwar KK.

Int J Cardiol. 2008 Apr 25;125(3):e44-7. Epub 2007 Apr 18.

PMID:
17445920
[PubMed - indexed for MEDLINE]
7.

[Profiles of genotypes of familial hypertrophic cardiomyopathy according to data of clinical studies].

Kipshidze NN, Liluashvili KN, Rogava MA.

Kardiologiia. 2010;50(3):65-70. Russian.

PMID:
20459408
[PubMed - indexed for MEDLINE]
8.

Noonan's cardiomyopathy: a non-hypertrophic variant.

Cooke RA, Chambers JB, Curry PV.

Br Heart J. 1994 Jun;71(6):561-5.

PMID:
8043339
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Images in cardiovascular medicine. Restrictive cardiomyopathy in familial amyloidosis TTR-Arg-50.

Singer R, Schnabel A, Strasser RH.

Circulation. 2003 Feb 4;107(4):643-4. No abstract available.

PMID:
12566380
[PubMed - indexed for MEDLINE]
Free Article
10.

Controversial issues in restrictive cardiomyopathy.

Shabetai R.

Postgrad Med J. 1992;68 Suppl 1:S47-51.

PMID:
1409216
[PubMed - indexed for MEDLINE]
11.

Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.

Hoedemaekers YM, Caliskan K, Majoor-Krakauer D, van de Laar I, Michels M, Witsenburg M, ten Cate FJ, Simoons ML, Dooijes D.

Eur Heart J. 2007 Nov;28(22):2732-7. Epub 2007 Oct 17.

PMID:
17947214
[PubMed - indexed for MEDLINE]
Free Article
12.

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.

Monserrat L, Hermida-Prieto M, Fernandez X, Rodríguez I, Dumont C, Cazón L, Cuesta MG, Gonzalez-Juanatey C, Peteiro J, Alvarez N, Penas-Lado M, Castro-Beiras A.

Eur Heart J. 2007 Aug;28(16):1953-61. Epub 2007 Jul 4.

PMID:
17611253
[PubMed - indexed for MEDLINE]
Free Article
13.

An atypical case of cardiomyopathy in a child: hypertrophic or restrictive cardiomyopathy?

Maki T, Niimura I, Nishikawa T, Sekiguchi M.

Heart Vessels Suppl. 1990;5:84-7.

PMID:
2093723
[PubMed - indexed for MEDLINE]
14.

[Genetics of inherited cardiomyopathies].

Richard P, Fressart V, Charron P, Hainque B.

Pathol Biol (Paris). 2010 Oct;58(5):343-52. doi: 10.1016/j.patbio.2009.10.010. Epub 2009 Nov 25. Review. French.

PMID:
19942368
[PubMed - indexed for MEDLINE]
15.

Titin mutation in familial restrictive cardiomyopathy.

Peled Y, Gramlich M, Yoskovitz G, Feinberg MS, Afek A, Polak-Charcon S, Pras E, Sela BA, Konen E, Weissbrod O, Geiger D, Gordon PM, Thierfelder L, Freimark D, Gerull B, Arad M.

Int J Cardiol. 2014 Jan 15;171(1):24-30. doi: 10.1016/j.ijcard.2013.11.037. Epub 2013 Nov 25.

PMID:
24315344
[PubMed - indexed for MEDLINE]
16.

Familial hypertrophic cardiomyopathy with atypical location: diagnosis by means of echocardiography and cardiovascular magnetic resonance.

Guler A, Tigen KM, Aung SM, Karabay CY, Karaahmet T, Kirma C.

Tex Heart Inst J. 2012;39(1):138-9. No abstract available.

PMID:
22412250
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology.

Olson TM, Karst ML, Whitby FG, Driscoll DJ.

Circulation. 2002 May 21;105(20):2337-40.

PMID:
12021217
[PubMed - indexed for MEDLINE]
Free Article
18.

A case of pediatric cardiomyopathy with severely restrictive physiology.

Nishikawa T, Tanaka Y, Sasaki Y, Kawataki M, Miyazawa Y, Yasui S, Takarada M, Kasajima T.

Heart Vessels. 1992;7(4):206-10.

PMID:
1487458
[PubMed - indexed for MEDLINE]
19.

Hypertrophic cardiomyopathy and planned in vitro fertilization. Genetic testing and clinical evaluation.

Zhu Hu J, Xiang Li J, Hong K, Xin Hu J, Brugada P, Shu Cheng X.

Herz. 2012 Jun;37(4):447-52. doi: 10.1007/s00059-011-3564-y.

PMID:
22301726
[PubMed - indexed for MEDLINE]
20.

Familial hypertrophic cardiomyopathy complicated by complete atrioventricular block.

Cicek D, Camsari A, Doven O.

Acta Cardiol. 2004 Feb;59(1):71-4.

PMID:
15030138
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk