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Results: 1 to 20 of 38

1.

Differences in global and regional left ventricular myocardial mechanics in various morphologic subtypes of patients with obstructive hypertrophic cardiomyopathy referred for ventricular septal myotomy/myectomy.

Kobayashi T, Dhillon A, Popovic Z, Bhonsale A, Smedira NG, Thamilarasan M, Lytle BW, Lever HM, Desai MY.

Am J Cardiol. 2014 Jun 1;113(11):1879-85. doi: 10.1016/j.amjcard.2014.03.020. Epub 2014 Mar 18.

PMID:
24837268
[PubMed - indexed for MEDLINE]
2.

Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.

Kumar S, Peters S, Thompson T, Morgan N, Maccicoca I, Trainer A, Zentner D, Kalman JM, Winship I, Vohra JK.

Heart Rhythm. 2013 Nov;10(11):1653-60. doi: 10.1016/j.hrthm.2013.08.022. Epub 2013 Aug 22.

PMID:
23973953
[PubMed - indexed for MEDLINE]
3.

Creatine kinase adenosine triphosphate and phosphocreatine energy supply in a single kindred of patients with hypertrophic cardiomyopathy.

Abraham MR, Bottomley PA, Dimaano VL, Pinheiro A, Steinberg A, Traill TA, Abraham TP, Weiss RG.

Am J Cardiol. 2013 Sep 15;112(6):861-6. doi: 10.1016/j.amjcard.2013.05.017. Epub 2013 Jun 7.

PMID:
23751935
[PubMed - indexed for MEDLINE]
4.

Late gadolinium enhancement cardiac magnetic resonance imaging in prognostic assessment of hypertrophic cardiomyopathy.

Bouabdallaoui N, Ennezat PV, Durand E, Puymirat E, Macron L.

Eur Heart J Cardiovasc Imaging. 2013 Oct;14(10):1024. doi: 10.1093/ehjci/jet067. Epub 2013 May 3. No abstract available.

PMID:
23644935
[PubMed - indexed for MEDLINE]
5.

Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing.

Jensen MK, Havndrup O, Christiansen M, Andersen PS, Diness B, Axelsson A, Skovby F, Køber L, Bundgaard H.

Circulation. 2013 Jan 1;127(1):48-54. doi: 10.1161/CIRCULATIONAHA.111.090514. Epub 2012 Nov 28.

PMID:
23197161
[PubMed - indexed for MEDLINE]
Free Article
6.

Long-term outcomes of patients bridged to recovery versus patients bridged to transplantation.

Birks EJ, George RS, Firouzi A, Wright G, Bahrami T, Yacoub MH, Khaghani A.

J Thorac Cardiovasc Surg. 2012 Jul;144(1):190-6. doi: 10.1016/j.jtcvs.2012.03.021. Epub 2012 Apr 11.

PMID:
22498081
[PubMed - indexed for MEDLINE]
7.

Cardiac and skeletal muscle expression of mutant β-myosin heavy chains, degree of functional impairment and phenotypic heterogeneity in hypertrophic cardiomyopathy.

Di Domenico M, Casadonte R, Ricci P, Santini M, Frati G, Rizzo A, Carratelli CR, Lamberti M, Parrotta E, Quaresima B, Faniello CM, Costanzo F, Cuda G.

J Cell Physiol. 2012 Oct;227(10):3471-6. doi: 10.1002/jcp.24047.

PMID:
22213221
[PubMed - indexed for MEDLINE]
8.

Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.

Christiaans I, Birnie E, Bonsel GJ, Mannens MM, Michels M, Majoor-Krakauer D, Dooijes D, van Tintelen JP, van den Berg MP, Volders PG, Arens YH, van den Wijngaard A, Atsma DE, Helderman-van den Enden AT, Houweling AC, de Boer K, van der Smagt JJ, Hauer RN, Marcelis CL, Timmermans J, van Langen IM, Wilde AA.

Eur Heart J. 2011 May;32(9):1161-70. doi: 10.1093/eurheartj/ehr092. Epub 2011 Apr 1.

PMID:
21459882
[PubMed - indexed for MEDLINE]
Free Article
9.

Pediatric emergency medicine: legal briefs.

Selbst SM.

Pediatr Emerg Care. 2010 Oct;26(10):778-81. doi: 10.1097/PEC.0b013e3181f4c15c. No abstract available.

PMID:
20930605
[PubMed - indexed for MEDLINE]
10.

Mitogenic cardiomyopathy: a lethal neonatal familial dilated cardiomyopathy characterized by myocyte hyperplasia and proliferation.

Chang KT, Taylor GP, Meschino WS, Kantor PF, Cutz E.

Hum Pathol. 2010 Jul;41(7):1002-8. doi: 10.1016/j.humpath.2009.12.008. Epub 2010 Mar 29.

PMID:
20303141
[PubMed - indexed for MEDLINE]
11.

Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.

Xu Q, Dewey S, Nguyen S, Gomes AV.

J Mol Cell Cardiol. 2010 May;48(5):899-909. doi: 10.1016/j.yjmcc.2010.03.005. Epub 2010 Mar 16. Review.

PMID:
20298698
[PubMed - indexed for MEDLINE]
12.

Association of angiotensin-converting enzyme activity and polymorphism with echocardiographic measures in familial and nonfamilial hypertrophic cardiomyopathy.

Buck PC, Fernandes F, Arteaga E, Matsumoto AY, Araujo AQ, Oliveira EM, Ianni BM, Ramires FJ, Krieger JE, Mady C.

Braz J Med Biol Res. 2009 Aug;42(8):717-21. Epub 2009 Apr 24.

PMID:
19390744
[PubMed - indexed for MEDLINE]
Free Article
13.

Evaluation of left atrial longitudinal function in patients with hypertrophic cardiomyopathy: a tissue Doppler imaging and two-dimensional strain study.

Paraskevaidis IA, Panou F, Papadopoulos C, Farmakis D, Parissis J, Ikonomidis I, Rigopoulos A, Iliodromitis EK, Th Kremastinos D.

Heart. 2009 Mar;95(6):483-9. doi: 10.1136/hrt.2008.146548. Epub 2008 Sep 2.

PMID:
18765436
[PubMed - indexed for MEDLINE]
14.

Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.

Brito D, Richard P, Komajda M, Madeira H.

Rev Port Cardiol. 2008 Feb;27(2):147-73. English, Portuguese.

PMID:
18488914
[PubMed - indexed for MEDLINE]
Free Article
15.
16.

Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.

Zahka K, Kalidas K, Simpson MA, Cross H, Keller BB, Galambos C, Gurtz K, Patton MA, Crosby AH.

Heart. 2008 Oct;94(10):1326-30. doi: 10.1136/hrt.2007.127241. Epub 2008 May 8.

PMID:
18467358
[PubMed - indexed for MEDLINE]
17.

A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy.

Fokstuen S, Lyle R, Munoz A, Gehrig C, Lerch R, Perrot A, Osterziel KJ, Geier C, Beghetti M, Mach F, Sztajzel J, Sigwart U, Antonarakis SE, Blouin JL.

Hum Mutat. 2008 Jun;29(6):879-85. doi: 10.1002/humu.20749.

PMID:
18409188
[PubMed - indexed for MEDLINE]
18.

Hypertrophic cardiomyopathy: the importance of arrhythmic events in patients at risk for sudden cardiac death.

Medeiros Pde T, Martinelli Filho M, Arteaga E, Costa R, Siqueira S, Mady C, Piegas LS, Ramires JA.

Arq Bras Cardiol. 2006 Nov;87(5):649-57. English, Portuguese.

PMID:
17221043
[PubMed - indexed for MEDLINE]
Free Article
19.

Familial premature coronary artery disease mortality and obstructive sleep apnea.

Gami AS, Rader S, Svatikova A, Wolk R, Herold DL, Huyber C, Winnicki M, Somers VK.

Chest. 2007 Jan;131(1):118-21.

PMID:
17218564
[PubMed - indexed for MEDLINE]
20.

Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.

D'Amico A, Graziano C, Pacileo G, Petrini S, Nowak KJ, Boldrini R, Jacques A, Feng JJ, Porfirio B, Sewry CA, Santorelli FM, Limongelli G, Bertini E, Laing N, Marston SB.

Neuromuscul Disord. 2006 Oct;16(9-10):548-52. Epub 2006 Sep 1.

PMID:
16945537
[PubMed - indexed for MEDLINE]

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