Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 107

1.

Deep basal inferoseptal crypts occur more commonly in patients with hypertrophic cardiomyopathy due to disease-causing myofilament mutations.

Deva DP, Williams LK, Care M, Siminovitch KA, Moshonov H, Wintersperger BJ, Rakowski H, Crean AM.

Radiology. 2013 Oct;269(1):68-76. doi: 10.1148/radiol.13122344. Epub 2013 Jun 14.

PMID:
23771913
[PubMed - indexed for MEDLINE]
2.

Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations.

Olivotto I, Girolami F, Sciagrà R, Ackerman MJ, Sotgia B, Bos JM, Nistri S, Sgalambro A, Grifoni C, Torricelli F, Camici PG, Cecchi F.

J Am Coll Cardiol. 2011 Aug 16;58(8):839-48. doi: 10.1016/j.jacc.2011.05.018.

PMID:
21835320
[PubMed - indexed for MEDLINE]
Free Article
3.

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.

Rai TS, Ahmad S, Bahl A, Ahuja M, Ahluwalia TS, Singh B, Talwar KK, Khullar M.

Mol Cell Biochem. 2009 Jan;321(1-2):189-96. doi: 10.1007/s11010-008-9932-0. Epub 2008 Oct 25.

PMID:
18953637
[PubMed - indexed for MEDLINE]
4.

Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations.

Binder J, Ommen SR, Gersh BJ, Van Driest SL, Tajik AJ, Nishimura RA, Ackerman MJ.

Mayo Clin Proc. 2006 Apr;81(4):459-67.

PMID:
16610565
[PubMed - indexed for MEDLINE]
5.

Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy.

Captur G, Lopes LR, Mohun TJ, Patel V, Li C, Bassett P, Finocchiaro G, Ferreira VM, Esteban MT, Muthurangu V, Sherrid MV, Day SM, Canter CE, McKenna WJ, Seidman CE, Bluemke DA, Elliott PM, Ho CY, Moon JC.

Circ Cardiovasc Imaging. 2014 Nov;7(6):863-71. doi: 10.1161/CIRCIMAGING.114.002411. Epub 2014 Sep 16.

PMID:
25228707
[PubMed - indexed for MEDLINE]
6.

Deformation patterns in genotyped patients with hypertrophic cardiomyopathy.

Geske JB, Bos JM, Gersh BJ, Ommen SR, Eidem BW, Ackerman MJ.

Eur Heart J Cardiovasc Imaging. 2014 Apr;15(4):456-65. doi: 10.1093/ehjci/jet234. Epub 2013 Nov 11.

PMID:
24217980
[PubMed - indexed for MEDLINE]
7.

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.

Andersen PS, Havndrup O, Hougs L, Sørensen KM, Jensen M, Larsen LA, Hedley P, Thomsen AR, Moolman-Smook J, Christiansen M, Bundgaard H.

Hum Mutat. 2009 Mar;30(3):363-70. doi: 10.1002/humu.20862.

PMID:
19035361
[PubMed - indexed for MEDLINE]
8.

Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.

Perrot A, Schmidt-Traub H, Hoffmann B, Prager M, Bit-Avragim N, Rudenko RI, Usupbaeva DA, Kabaeva Z, Imanov B, Mirrakhimov MM, Dietz R, Wycisk A, Tendera M, Gessner R, Osterziel KJ.

J Mol Med (Berl). 2005 Jun;83(6):468-77. Epub 2005 Apr 22.

PMID:
15856146
[PubMed - indexed for MEDLINE]
9.

Genetic diagnosis of hypertrophic cardiomyopathy using mass spectrometry DNA arrays and high resolution melting.

Santos S, Lança V, Oliveira H, Branco P, Silveira L, Marques V, Brito D, Madeira H, Bicho M, Fernandes AR.

Rev Port Cardiol. 2011 Jan;30(1):7-18.

PMID:
21425739
[PubMed - indexed for MEDLINE]
Free Article
10.

[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].

Laredo R, Monserrat L, Hermida-Prieto M, Fernández X, Rodríguez I, Cazón L, Alvariño I, Dumont C, Piñón P, Peteiro J, Bouzas B, Castro-Beiras A.

Rev Esp Cardiol. 2006 Oct;59(10):1008-18. Spanish. Erratum in: Rev Esp Cardiol. 2007 May;60(5):557.

PMID:
17125710
[PubMed - indexed for MEDLINE]
Free Article
11.

Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations.

Germans T, Wilde AA, Dijkmans PA, Chai W, Kamp O, Pinto YM, van Rossum AC.

J Am Coll Cardiol. 2006 Dec 19;48(12):2518-23. Epub 2006 Nov 28.

PMID:
17174192
[PubMed - indexed for MEDLINE]
Free Article
12.

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy.

Van Driest SL, Ackerman MJ, Ommen SR, Shakur R, Will ML, Nishimura RA, Tajik AJ, Gersh BJ.

Circulation. 2002 Dec 10;106(24):3085-90.

PMID:
12473556
[PubMed - indexed for MEDLINE]
Free Article
13.

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.

Kubo T, Gimeno JR, Bahl A, Steffensen U, Steffensen M, Osman E, Thaman R, Mogensen J, Elliott PM, Doi Y, McKenna WJ.

J Am Coll Cardiol. 2007 Jun 26;49(25):2419-26. Epub 2007 Jun 11.

PMID:
17599605
[PubMed - indexed for MEDLINE]
Free Article
14.

Prevalence and clinical profile of myocardial crypts in hypertrophic cardiomyopathy.

Maron MS, Rowin EJ, Lin D, Appelbaum E, Chan RH, Gibson CM, Lesser JR, Lindberg J, Haas TS, Udelson JE, Manning WJ, Maron BJ.

Circ Cardiovasc Imaging. 2012 Jul;5(4):441-7. doi: 10.1161/CIRCIMAGING.112.972760. Epub 2012 May 4.

PMID:
22563033
[PubMed - indexed for MEDLINE]
Free Article
15.

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.

Van Driest SL, Jaeger MA, Ommen SR, Will ML, Gersh BJ, Tajik AJ, Ackerman MJ.

J Am Coll Cardiol. 2004 Aug 4;44(3):602-10.

PMID:
15358028
[PubMed - indexed for MEDLINE]
16.

Coronary telangiectasia associated with hypertrophic cardiomyopathy.

Frustaci A, Lanfranchi G, Bellin M, Chimenti C.

Eur J Heart Fail. 2012 Dec;14(12):1332-7. doi: 10.1093/eurjhf/hfs125. Epub 2012 Aug 5.

PMID:
22869457
[PubMed - indexed for MEDLINE]
17.

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.

Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F.

J Cardiovasc Med (Hagerstown). 2006 Aug;7(8):601-7.

PMID:
16858239
[PubMed - indexed for MEDLINE]
18.

Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives.

Maron BJ, Maron MS, Semsarian C.

J Am Coll Cardiol. 2012 Aug 21;60(8):705-15. doi: 10.1016/j.jacc.2012.02.068. Epub 2012 Jul 11. Review.

PMID:
22796258
[PubMed - indexed for MEDLINE]
Free Article
19.

Long-term outcome of 4 Korean families with hypertrophic cardiomyopathy caused by 4 different mutations.

Choi JO, Yu CW, Chun Nah J, Rang Park J, Lee BS, Jeong Choi Y, Cho BR, Lee SC, Woo Park S, Kimura A, Euy Park J.

Clin Cardiol. 2010 Jul;33(7):430-8. doi: 10.1002/clc.20795.

PMID:
20641121
[PubMed - indexed for MEDLINE]
20.

Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure.

Arbustini E, Fasani R, Morbini P, Diegoli M, Grasso M, Dal Bello B, Marangoni E, Banfi P, Banchieri N, Bellini O, Comi G, Narula J, Campana C, Gavazzi A, Danesino C, Viganò M.

Heart. 1998 Dec;80(6):548-58. Erratum in: Heart 1999 Mar;81(3):330.

PMID:
10065021
[PubMed - indexed for MEDLINE]
Free PMC Article
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk