Behr ER - Search Results

1

Role of invasive EP testing in the evaluation and management of hypertrophic cardiomyopathy.

Behr ER, Elliott P, McKenna WJ. Behr ER, et al. Card Electrophysiol Rev. 2002 Dec;6(4):482-6. doi: 10.1023/a:1021161114347. Card Electrophysiol Rev. 2002. PMID: 12438832 Review.

2

Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death.

McKenna WJ, Behr ER. McKenna WJ, et al. Among authors: behr er. Heart. 2002 Feb;87(2):169-76. doi: 10.1136/heart.87.2.169. Heart. 2002. PMID: 11796562 Free PMC article. Review. No abstract available.

3

Hypertrophic Cardiomyopathy.

Behr ER, McKenna WJ. Behr ER, et al. Curr Treat Options Cardiovasc Med. 2002 Dec;4(6):443-453. doi: 10.1007/s11936-002-0039-8. Curr Treat Options Cardiovasc Med. 2002. PMID: 12408787

4

Elite athletes with recurrent ERS.

Firoozi S, Behr E, McKenna W. Firoozi S, et al. Eur Heart J. 2003 Apr;24(8):783; author reply 783-4. doi: 10.1016/s0195-668x(02)00651-6. Eur Heart J. 2003. PMID: 12713771 No abstract available.

5

Genetic risk for acquired arrhythmia.

Behr ER, McKenna WJ. Behr ER, et al. Trends Genet. 2003 Sep;19(9):470-3. doi: 10.1016/S0168-9525(03)00200-2. Trends Genet. 2003. PMID: 12957537 No abstract available.

6

Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome.

Behr E, Wood DA, Wright M, Syrris P, Sheppard MN, Casey A, Davies MJ, McKenna W; Sudden Arrhythmic Death Syndrome Steering Group. Behr E, et al. Lancet. 2003 Nov 1;362(9394):1457-9. doi: 10.1016/s0140-6736(03)14692-2. Lancet. 2003. PMID: 14602442

7

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.

Hofman-Bang J, Behr ER, Hedley P, Tfelt-Hansen J, Kanters JK, Haunsøe S, McKenna WJ, Christiansen M. Hofman-Bang J, et al. Among authors: behr er. Clin Genet. 2006 Jun;69(6):504-11. doi: 10.1111/j.1399-0004.2006.00621.x. Clin Genet. 2006. PMID: 16712702

8

Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death.

Behr ER, Casey A, Sheppard M, Wright M, Bowker TJ, Davies MJ, McKenna WJ, Wood DA. Behr ER, et al. Heart. 2007 May;93(5):601-5. doi: 10.1136/hrt.2006.099598. Epub 2007 Jan 19. Heart. 2007. PMID: 17237131 Free PMC article.

9

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

Behr ER, Dalageorgou C, Christiansen M, Syrris P, Hughes S, Tome Esteban MT, Rowland E, Jeffery S, McKenna WJ. Behr ER, et al. Eur Heart J. 2008 Jul;29(13):1670-80. doi: 10.1093/eurheartj/ehn219. Epub 2008 May 27. Eur Heart J. 2008. PMID: 18508782

10

Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.

Simpson MA, Mansour S, Ahnood D, Kalidas K, Patton MA, McKenna WJ, Behr ER, Crosby AH. Simpson MA, et al. Among authors: behr er. Cardiology. 2009;113(1):28-34. doi: 10.1159/000165696. Epub 2008 Oct 29. Cardiology. 2009. PMID: 18957847

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