Schulze-Bahr E - Search Results

1

Molecular diagnosis in a child with sudden infant death syndrome.

Schwartz PJ, Priori SG, Bloise R, Napolitano C, Ronchetti E, Piccinini A, Goj C, Breithardt G, Schulze-Bahr E, Wedekind H, Nastoli J. Schwartz PJ, et al. Lancet. 2001 Oct 20;358(9290):1342-3. doi: 10.1016/S0140-6736(01)06450-9. Lancet. 2001. PMID: 11684219

2

Gene-specific differences in the circadian variation of ventricular repolarization in the long QT syndrome: a key to sudden death during sleep?

Stramba-Badiale M, Priori SG, Napolitano C, Locati EH, Viñolas X, Haverkamp W, Schulze-Bahr E, Goulene K, Schwartz PJ. Stramba-Badiale M, et al. Ital Heart J. 2000 May;1(5):323-8. Ital Heart J. 2000. PMID: 10832806

3

De novo mutation in the SCN5A gene associated with early onset of sudden infant death.

Wedekind H, Smits JP, Schulze-Bahr E, Arnold R, Veldkamp MW, Bajanowski T, Borggrefe M, Brinkmann B, Warnecke I, Funke H, Bhuiyan ZA, Wilde AA, Breithardt G, Haverkamp W. Wedekind H, et al. Circulation. 2001 Sep 4;104(10):1158-64. doi: 10.1161/hc3501.095361. Circulation. 2001. PMID: 11535573

4

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA. Chen Q, et al. Circulation. 1999 Mar 16;99(10):1344-7. doi: 10.1161/01.cir.99.10.1344. Circulation. 1999. PMID: 10077519

5

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating MT, Towbin JA, Beggs AH, Brink P, Wilde AA, Toivonen L, Zareba W, Robinson JL, Timothy KW, Corfield V, Wattanasirichaigoon D, Corbett C, Haverkamp W, Schulze-Bahr E, Lehmann MH, Schwartz K, Coumel P, Bloise R. Schwartz PJ, et al. Circulation. 2001 Jan 2;103(1):89-95. doi: 10.1161/01.cir.103.1.89. Circulation. 2001. PMID: 11136691 Clinical Trial.

6

Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response.

Schulze-Bahr E, Fenge H, Etzrodt D, Haverkamp W, Mönnig G, Wedekind H, Breithardt G, Kehl HG. Schulze-Bahr E, et al. Heart. 2004 Jan;90(1):13-6. doi: 10.1136/heart.90.1.13. Heart. 2004. PMID: 14676229 Free PMC article.

7

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H. Schulze-Bahr E, et al. Z Kardiol. 1999 Apr;88(4):245-54. doi: 10.1007/s003920050283. Z Kardiol. 1999. PMID: 10408028 Review.

8

[Clinical aspects and molecular genetics of the long QT-syndrome].

Haverkamp W, Mönnig G, Wedekind H, Schulze-Bahr E, Borggrefe M, Assmann G, Funke H, Breithardt G. Haverkamp W, et al. Dtsch Med Wochenschr. 1999 Aug 20;124(33):972-9. doi: 10.1055/s-2007-1024461. Dtsch Med Wochenschr. 1999. PMID: 10481758 Review. German. No abstract available.

9

[18-year old patient with anti-epileptic therapy and sudden cardiac death].

Witzenbichler B, Schulze-Bahr E, Haverkamp W, Breithardt G, Sticherling C, Behrens S, Schultheiss HP. Witzenbichler B, et al. Z Kardiol. 2003 Sep;92(9):747-53. doi: 10.1007/s00392-003-0961-0. Z Kardiol. 2003. PMID: 14508592 German.

10

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous.

Schulze-Bahr E, Haverkamp W, Wedekind H, Rubie C, Hördt M, Borggrefe M, Assmann G, Breithardt G, Funke H. Schulze-Bahr E, et al. Hum Genet. 1997 Oct;100(5-6):573-6. doi: 10.1007/s004390050554. Hum Genet. 1997. PMID: 9341873

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