Behr ER - Search Results

1

The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.

Hedley PL, Kanters JK, Dembic M, Jespersen T, Skibsbye L, Aidt FH, Eschen O, Graff C, Behr ER, Schlamowitz S, Corfield V, McKenna WJ, Christiansen M. Hedley PL, et al. Among authors: behr er. Circ Cardiovasc Genet. 2013 Oct;6(5):452-61. doi: 10.1161/CIRCGENETICS.113.000137. Epub 2013 Sep 10. Circ Cardiovasc Genet. 2013. PMID: 24021552

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

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.

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

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

7

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

8

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

9

Therapeutic hypothermia and ventricular fibrillation storm in early repolarization syndrome.

Bastiaenen R, Hedley PL, Christiansen M, Behr ER. Bastiaenen R, et al. Among authors: behr er. Heart Rhythm. 2010 Jun;7(6):832-4. doi: 10.1016/j.hrthm.2010.02.037. Epub 2010 Mar 3. Heart Rhythm. 2010. PMID: 20206297 No abstract available.

10

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.

Nyegaard M, Overgaard MT, Søndergaard MT, Vranas M, Behr ER, Hildebrandt LL, Lund J, Hedley PL, Camm AJ, Wettrell G, Fosdal I, Christiansen M, Børglum AD. Nyegaard M, et al. Among authors: behr er. Am J Hum Genet. 2012 Oct 5;91(4):703-12. doi: 10.1016/j.ajhg.2012.08.015. Am J Hum Genet. 2012. PMID: 23040497 Free PMC article.

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