Assmann G - Search Results

1

Molecular genetics of arrhythmias--a new paradigm.

Schulze-Bahr E, Haverkamp W, Borggrefe M, Wedekind H, Mönnig G, Mergenthaler J, Assmann G, Funke H, Breithardt G. Schulze-Bahr E, et al. Among authors: assmann g. Z Kardiol. 2000;89 Suppl 4:IV12-22. doi: 10.1007/s003920070059. Z Kardiol. 2000. PMID: 10810773 Review.

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: assmann g. J Mol Med (Berl). 1995 Nov;73(11):565-9. doi: 10.1007/BF00195141. J Mol Med (Berl). 1995. PMID: 8751140

3

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. Among authors: assmann g. Z Kardiol. 1999 Apr;88(4):245-54. doi: 10.1007/s003920050283. Z Kardiol. 1999. PMID: 10408028 Review.

4

[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. Among authors: assmann g. 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.

5

[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome].

Mönnig G, Schulze-Bahr E, Wedekind H, Eckardt L, Kirchhof P, Funke H, Kotthoff S, Vogt J, Assmann G, Breithardt G, Haverkamp W. Mönnig G, et al. Among authors: assmann g. Z Kardiol. 2002 May;91(5):380-8. doi: 10.1007/s00392-002-0789-z. Z Kardiol. 2002. PMID: 12132284 Review. German.

6

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: assmann g. Hum Genet. 1997 Oct;100(5-6):573-6. doi: 10.1007/s004390050554. Hum Genet. 1997. PMID: 9341873

7

Strategies for the assessment of genetic coronary artery disease risk.

Funke H, Assmann G. Funke H, et al. Among authors: assmann g. Curr Opin Lipidol. 1999 Jun;10(3):285-91. doi: 10.1097/00041433-199906000-00011. Curr Opin Lipidol. 1999. PMID: 10431665 Review.

8

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: assmann g. 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

9

[Coronary angiography and intravascular ultrasound examination of a 60-year-old patient with familial HDL deficiency (Tangier disease)].

Walter M, Kerber S, Fechtrup C, Seedorf U, Breithardt G, Assmann G. Walter M, et al. Among authors: assmann g. Z Kardiol. 1994 May;83(5):381-5. Z Kardiol. 1994. PMID: 8053248 German.

10

Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection.

Rust S, Funke H, Assmann G. Rust S, et al. Among authors: assmann g. Nucleic Acids Res. 1993 Aug 11;21(16):3623-9. doi: 10.1093/nar/21.16.3623. Nucleic Acids Res. 1993. PMID: 8367277 Free PMC article.

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