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Items: 1 to 20 of 162

1.

Molecular autopsy in young sudden cardiac death victims with suspected cardiomyopathy.

Larsen MK, Nissen PH, Berge KE, Leren TP, Kristensen IB, Jensen HK, Banner J.

Forensic Sci Int. 2012 Jun 10;219(1-3):33-8. doi: 10.1016/j.forsciint.2011.11.020. Epub 2011 Dec 15.

PMID:
22177269
2.

Disease penetrance and risk stratification for sudden cardiac death in asymptomatic hypertrophic cardiomyopathy mutation carriers.

Michels M, Soliman OI, Phefferkorn J, Hoedemaekers YM, Kofflard MJ, Dooijes D, Majoor-Krakauer D, Ten Cate FJ.

Eur Heart J. 2009 Nov;30(21):2593-8. doi: 10.1093/eurheartj/ehp306. Epub 2009 Aug 6.

PMID:
19666645
3.

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.

4.

Phenotype-driven molecular autopsy for sudden cardiac death.

Cann F, Corbett M, O'Sullivan D, Tennant S, Hailey H, Grieve JH, Broadhurst P, Rankin R, Dean JC.

Clin Genet. 2017 Jan;91(1):22-29. doi: 10.1111/cge.12778. Epub 2016 May 11.

PMID:
27000522
5.

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
6.

[Analysis of MYH7, MYBPC3 and TNNT2 gene mutations in 10 Chinese pedigrees with familial hypertrophic cardiomyopathy and the correlation between genotype and phenotype].

Liu WL, Xie WL, Hu DY, Zhu TG, Li YT, Sun YH, Li CL, Li L, Li TC, Bian H, Tong QG, Yang SN, Fan RY, Cui W.

Zhonghua Xin Xue Guan Bing Za Zhi. 2006 Mar;34(3):202-7. Chinese.

PMID:
16630449
7.

PKP2 mutations in sudden death from arrhythmogenic right ventricular cardiomyopathy (ARVC) and sudden unexpected death with negative autopsy (SUDNA).

Zhang M, Tavora F, Oliveira JB, Li L, Franco M, Fowler D, Zhao Z, Burke A.

Circ J. 2012;76(1):189-94. Epub 2011 Oct 22.

8.

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

Allegue C, Gil R, Blanco-Verea A, Santori M, Rodríguez-Calvo M, Concheiro L, Carracedo A, Brion M.

Int J Legal Med. 2011 Jul;125(4):565-72. doi: 10.1007/s00414-011-0572-7. Epub 2011 Apr 16.

PMID:
21499742
9.

Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart.

Hertz CL, Christiansen SL, Ferrero-Miliani L, Dahl M, Weeke PE; LuCamp, Ottesen GL, Frank-Hansen R, Bundgaard H, Morling N.

Int J Legal Med. 2016 Jan;130(1):91-102. doi: 10.1007/s00414-015-1261-8. Epub 2015 Sep 17.

PMID:
26383259
10.

Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.

Zhao Y, Cao H, Song Y, Feng Y, Ding X, Pang M, Zhang Y, Zhang H, Ding J, Xia X.

Int J Mol Med. 2016 Jun;37(6):1511-20. doi: 10.3892/ijmm.2016.2565. Epub 2016 Apr 14.

11.

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.

Waldmüller S, Sakthivel S, Saadi AV, Selignow C, Rakesh PG, Golubenko M, Joseph PK, Padmakumar R, Richard P, Schwartz K, Tharakan JM, Rajamanickam C, Vosberg HP.

J Mol Cell Cardiol. 2003 Jun;35(6):623-36.

PMID:
12788380
12.

Genetic anticipation in a special form of hypertrophic cardiomyopathy with sudden cardiac death in a family with 74 members across 5 generations.

Guo X, Fan C, Wang Y, Wang M, Cai C, Yang Y, Zhao S, Duan F, Li Y.

Medicine (Baltimore). 2017 Mar;96(11):e6249. doi: 10.1097/MD.0000000000006249.

13.

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
14.

A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India.

Bashyam MD, Purushotham G, Chaudhary AK, Rao KM, Acharya V, Mohammad TA, Nagarajaram HA, Hariram V, Narasimhan C.

Mol Cell Biochem. 2012 Jan;360(1-2):373-82. doi: 10.1007/s11010-011-1077-x. Epub 2011 Sep 29.

PMID:
21959974
15.

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.

16.

Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.

Forleo C, Carmosino M, Resta N, Rampazzo A, Valecce R, Sorrentino S, Iacoviello M, Pisani F, Procino G, Gerbino A, Scardapane A, Simone C, Calore M, Torretta S, Svelto M, Favale S.

PLoS One. 2015 Apr 2;10(4):e0121723. doi: 10.1371/journal.pone.0121723. eCollection 2015.

17.

A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.

Hertz CL, Ferrero-Miliani L, Frank-Hansen R, Morling N, Bundgaard H.

Europace. 2015 Mar;17(3):350-7. doi: 10.1093/europace/euu210. Epub 2014 Oct 26. Review.

PMID:
25345827
18.

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

Roberts JD, Veinot JP, Rutberg J, Gollob MH.

Cardiovasc Pathol. 2010 Sep-Oct;19(5):316-20. doi: 10.1016/j.carpath.2009.06.003. Epub 2009 Jul 24.

PMID:
19632136
19.

[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.

20.

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.

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