Borggrefe M - Search Results

1

Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.

Isbrandt D, Friederich P, Solth A, Haverkamp W, Ebneth A, Borggrefe M, Funke H, Sauter K, Breithardt G, Pongs O, Schulze-Bahr E. Isbrandt D, et al. Among authors: borggrefe m. J Mol Med (Berl). 2002 Aug;80(8):524-32. doi: 10.1007/s00109-002-0364-0. Epub 2002 Jun 28. J Mol Med (Berl). 2002. PMID: 12185453

2

Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome.

Schulze-Bahr E, Haverkamp W, Wiebusch H, Schulte H, Hördt M, Borggrefe M, Breithardt G, Assmann G, Funke H. Schulze-Bahr E, et al. Among authors: borggrefe m. J Mol Med (Berl). 1995 Nov;73(11):565-9. doi: 10.1007/BF00195141. J Mol Med (Berl). 1995. PMID: 8751140

3

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. Among authors: borggrefe m. Hum Genet. 1997 Oct;100(5-6):573-6. doi: 10.1007/s004390050554. Hum Genet. 1997. PMID: 9341873

4

Multistep-touchdown vectorette-PCR--a rapid technique for the identification of IVS in genes.

Rubie C, Schulze-Bahr E, Wedekind H, Borggrefe M, Haverkamp W, Breithardt G. Rubie C, et al. Among authors: borggrefe m. Biotechniques. 1999 Sep;27(3):414-6, 418. doi: 10.2144/99273bm03. Biotechniques. 1999. PMID: 10489595 Free article. No abstract available.

5

Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome.

Moennig G, Schulze-Bahr E, Wedekind H, Borggrefe M, Funke H, Toelle M, Kirchhof P, Eckardt L, Assmann G, Breithardt G, Haverkamp W. Moennig G, et al. Among authors: borggrefe m. Pacing Clin Electrophysiol. 2001 Apr;24(4 Pt 1):406-15. doi: 10.1046/j.1460-9592.2001.00406.x. Pacing Clin Electrophysiol. 2001. PMID: 11341076

6

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. Among authors: borggrefe m. Circulation. 2001 Sep 4;104(10):1158-64. doi: 10.1161/hc3501.095361. Circulation. 2001. PMID: 11535573

7

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. Among authors: borggrefe m. Pacing Clin Electrophysiol. 2003 Oct;26(10):2033-5. doi: 10.1046/j.1460-9592.2003.00313.x. Pacing Clin Electrophysiol. 2003. PMID: 14516346

8

Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.

Schulze-Bahr E, Eckardt L, Breithardt G, Seidl K, Wichter T, Wolpert C, Borggrefe M, Haverkamp W. Schulze-Bahr E, et al. Among authors: borggrefe m. Hum Mutat. 2003 Jun;21(6):651-2. doi: 10.1002/humu.9144. Hum Mutat. 2003. PMID: 14961552

9

Electrophysiologic effects of potassium channel openers.

Haverkamp W, Borggrefe M, Breithardt G. Haverkamp W, et al. Among authors: borggrefe m. Cardiovasc Drugs Ther. 1995 Mar;9 Suppl 2:195-202. doi: 10.1007/BF00878466. Cardiovasc Drugs Ther. 1995. PMID: 7647023 Review.

10

Blocking effects of the antiarrhythmic drug propafenone on the HERG potassium channel.

Mergenthaler J, Haverkamp W, Hüttenhofer A, Skryabin BV, Musshoff U, Borggrefe M, Speckmann EJ, Breithardt G, Madeja M. Mergenthaler J, et al. Among authors: borggrefe m. Naunyn Schmiedebergs Arch Pharmacol. 2001 Apr;363(4):472-80. doi: 10.1007/s002100000392. Naunyn Schmiedebergs Arch Pharmacol. 2001. PMID: 11330342

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