Behr ER - Search Results

1

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

Tester DJ, Wong LCH, Chanana P, Jaye A, Evans JM, FitzPatrick DR, Evans MJ, Fleming P, Jeffrey I, Cohen MC, Tfelt-Hansen J, Simpson MA, Behr ER, Ackerman MJ. Tester DJ, et al. Among authors: behr er. J Am Coll Cardiol. 2018 Mar 20;71(11):1217-1227. doi: 10.1016/j.jacc.2018.01.030. J Am Coll Cardiol. 2018. PMID: 29544605 Free article.

2

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

3

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.

4

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

5

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

6

Low prevalence of risk markers in cases of sudden death due to Brugada syndrome relevance to risk stratification in Brugada syndrome.

Raju H, Papadakis M, Govindan M, Bastiaenen R, Chandra N, O'Sullivan A, Baines G, Sharma S, Behr ER. Raju H, et al. Among authors: behr er. J Am Coll Cardiol. 2011 Jun 7;57(23):2340-5. doi: 10.1016/j.jacc.2010.11.067. J Am Coll Cardiol. 2011. PMID: 21636035 Free article.

7

Acquired long QT syndrome: as risky as congenital long QT syndrome?

Wong LC, Behr ER. Wong LC, et al. Among authors: behr er. Europace. 2012 Mar;14(3):310-1. doi: 10.1093/europace/eur372. Epub 2011 Nov 20. Europace. 2012. PMID: 22106361 No abstract available.

8

Specificity of elevated intercostal space ECG recording for the type 1 Brugada ECG pattern.

Holst AG, Tangø M, Batchvarov V, Govindan M, Haunsø S, Svendsen JH, Behr ER, Tfelt-Hansen J. Holst AG, et al. Among authors: behr er. Ann Noninvasive Electrocardiol. 2012 Apr;17(2):108-12. doi: 10.1111/j.1542-474X.2012.00499.x. Ann Noninvasive Electrocardiol. 2012. PMID: 22537328 Free PMC article.

9

Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia.

Jamshidi Y, Nolte IM, Dalageorgou C, Zheng D, Johnson T, Bastiaenen R, Ruddy S, Talbott D, Norris KJ, Snieder H, George AL, Marshall V, Shakir S, Kannankeril PJ, Munroe PB, Camm AJ, Jeffery S, Roden DM, Behr ER. Jamshidi Y, et al. Among authors: behr er. J Am Coll Cardiol. 2012 Aug 28;60(9):841-50. doi: 10.1016/j.jacc.2012.03.031. Epub 2012 Jun 6. J Am Coll Cardiol. 2012. PMID: 22682551 Free PMC article.

10

Unexplained sudden death, focussing on genetics and family phenotyping.

Raju H, Behr ER. Raju H, et al. Among authors: behr er. Curr Opin Cardiol. 2013 Jan;28(1):19-25. doi: 10.1097/HCO.0b013e32835b0a9e. Curr Opin Cardiol. 2013. PMID: 23128498 Review.

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