Schulze-Bahr E - Search Results

1

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.

Kolder ICRM, Tanck MWT, Postema PG, Barc J, Sinner MF, Zumhagen S, Husemann A, Stallmeyer B, Koopmann TT, Hofman N, Pfeufer A, Lichtner P, Meitinger T, Beckmann BM, Myerburg RJ, Bishopric NH, Roden DM, Kääb S, Wilde AAM, Schott JJ, Schulze-Bahr E, Bezzina CR. Kolder ICRM, et al. Circ Cardiovasc Genet. 2015 Jun;8(3):447-456. doi: 10.1161/CIRCGENETICS.114.000785. Epub 2015 Mar 3. Circ Cardiovasc Genet. 2015. PMID: 25737393 Free PMC article.

2

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.

Smits JP, Eckardt L, Probst V, Bezzina CR, Schott JJ, Remme CA, Haverkamp W, Breithardt G, Escande D, Schulze-Bahr E, LeMarec H, Wilde AA. Smits JP, et al. J Am Coll Cardiol. 2002 Jul 17;40(2):350-6. doi: 10.1016/s0735-1097(02)01962-9. J Am Coll Cardiol. 2002. PMID: 12106943 Free article.

3

Electrical alternans in long QT syndrome resembling a Brugada syndrome pattern.

Schulze-Bahr E, Zoelch KA, Eckardt L, Haverkamp W, Breithardt G, Borggrefe M. Schulze-Bahr E, et al. Pacing Clin Electrophysiol. 2003 Oct;26(10):2033-5. doi: 10.1046/j.1460-9592.2003.00313.x. Pacing Clin Electrophysiol. 2003. PMID: 14516346

4

Susceptibility genes and modifiers for cardiac arrhythmias.

Kääb S, Schulze-Bahr E. Kääb S, et al. Cardiovasc Res. 2005 Aug 15;67(3):397-413. doi: 10.1016/j.cardiores.2005.04.005. Cardiovasc Res. 2005. PMID: 15949790 Review.

5

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C, Engeland B, Mönnig G, Haverkamp W, Brinkmann B, Schulze-Bahr E. Wedekind H, et al. Int J Legal Med. 2006 May;120(3):129-37. doi: 10.1007/s00414-005-0019-0. Epub 2005 Jul 13. Int J Legal Med. 2006. PMID: 16012827

6

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome.

Smits JP, Veldkamp MW, Bezzina CR, Bhuiyan ZA, Wedekind H, Schulze-Bahr E, Wilde AA. Smits JP, et al. Cardiovasc Res. 2005 Aug 15;67(3):459-66. doi: 10.1016/j.cardiores.2005.01.017. Cardiovasc Res. 2005. PMID: 16039271

7

Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome.

Verkerk AO, Wilders R, Schulze-Bahr E, Beekman L, Bhuiyan ZA, Bertrand J, Eckardt L, Lin D, Borggrefe M, Breithardt G, Mannens MM, Tan HL, Wilde AA, Bezzina CR. Verkerk AO, et al. Cardiovasc Res. 2005 Dec 1;68(3):441-53. doi: 10.1016/j.cardiores.2005.06.027. Epub 2005 Jul 25. Cardiovasc Res. 2005. PMID: 16043162

8

Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implications.

Tan HL, Bardai A, Shimizu W, Moss AJ, Schulze-Bahr E, Noda T, Wilde AA. Tan HL, et al. Circulation. 2006 Nov 14;114(20):2096-103. doi: 10.1161/CIRCULATIONAHA.106.642694. Epub 2006 Nov 6. Circulation. 2006. PMID: 17088455

9

Female predominance and transmission distortion in the long-QT syndrome.

Imboden M, Swan H, Denjoy I, Van Langen IM, Latinen-Forsblom PJ, Napolitano C, Fressart V, Breithardt G, Berthet M, Priori S, Hainque B, Wilde AA, Schulze-Bahr E, Feingold J, Guicheney P. Imboden M, et al. N Engl J Med. 2006 Dec 28;355(26):2744-51. doi: 10.1056/NEJMoa042786. N Engl J Med. 2006. PMID: 17192539 Free article.

10

Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data.

Paul M, Gerss J, Schulze-Bahr E, Wichter T, Vahlhaus C, Wilde AA, Breithardt G, Eckardt L. Paul M, et al. Eur Heart J. 2007 Sep;28(17):2126-33. doi: 10.1093/eurheartj/ehm116. Epub 2007 May 5. Eur Heart J. 2007. PMID: 17483540 Review.

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