Maruhn-Debowski B - Search Results

1

The TT genotype of the C677T polymorphism in the methylentetrahydrofolate reductase as a risk factor in thrombotic microangiopathies: results from a pilot study.

Sucker C, Kurschat C, Farokhzad F, Hetzel GR, Grabensee B, Maruhn-Debowski B, Loncar R, Scharf RE, Zotz RB. Sucker C, et al. Among authors: maruhn debowski b. Clin Appl Thromb Hemost. 2009 May-Jun;15(3):283-8. doi: 10.1177/1076029607308865. Clin Appl Thromb Hemost. 2009. PMID: 19448163 Free article.

2

Association of genotypes of thrombin-activatable fibrinolysis inhibitors with thrombotic microangiopathies--a pilot study.

Sucker C, Hetzel GR, Farokhzad F, Dahhan F, Schmitz M, Kurschat C, Grabensee B, Maruhn-Debowski B, Zotz R, Scharf R. Sucker C, et al. Among authors: maruhn debowski b. Nephrol Dial Transplant. 2007 May;22(5):1347-50. doi: 10.1093/ndt/gfl753. Epub 2007 Feb 27. Nephrol Dial Transplant. 2007. PMID: 17327284

3

The homozygous leu variant of the factor XIII Val34Leu polymorphism as a risk factor for the manifestation of thrombotic microangiopathies.

Sucker C, Farokhzad F, Kurschat C, Grabensee B, Scharf RE, Zotz RB, Maruhn-Debowski B, Hetzel GR. Sucker C, et al. Among authors: maruhn debowski b. Clin Appl Thromb Hemost. 2009 Mar-Apr;15(2):197-200. doi: 10.1177/1076029607304723. Epub 2007 Sep 25. Clin Appl Thromb Hemost. 2009. PMID: 17895511 Free article.

4

Are prothrombotic variants of platelet glycoprotein receptor polymorphisms involved in the pathogenesis of thrombotic microangiopathies?

Sucker C, Schmitz M, Hetzel GR, Grabensee B, Maruhn-Debowski B, Ostojic L, Scharf RE, Zotz RB. Sucker C, et al. Among authors: maruhn debowski b. Clin Appl Thromb Hemost. 2009 Jul-Aug;15(4):402-7. doi: 10.1177/1076029608316015. Epub 2008 May 22. Clin Appl Thromb Hemost. 2009. PMID: 18502778 Free article.

5

The G1691A mutation of the factor V gene (factor V Leiden) and the G20210A mutation of the prothrombin gene as risk factors in thrombotic microangiopathies.

Sucker C, Kurschat C, Hetzel GR, Grabensee B, Maruhn-Debowski B, Loncar R, Ostojic L, Scharf RE, Zotz RB. Sucker C, et al. Among authors: maruhn debowski b. Clin Appl Thromb Hemost. 2009 May-Jun;15(3):360-3. doi: 10.1177/1076029607311778. Clin Appl Thromb Hemost. 2009. PMID: 19448164 Free article.

6

Mutation in the gene coding for coagulation factor V and resistance to activated protein C: detection of the genetic mutation by oligonucleotide ligation assay using a semi-automated system.

Zotz RB, Maruhn-Debowski B, Scharf RE. Zotz RB, et al. Among authors: maruhn debowski b. Thromb Haemost. 1996 Jul;76(1):53-5. Thromb Haemost. 1996. PMID: 8819251

7

Polymorphism of platelet membrane glycoprotein IIIa: human platelet antigen 1b (HPA-1b/PlA2) is an inherited risk factor for premature myocardial infarction in coronary artery disease.

Zotz RB, Winkelmann BR, Nauck M, Giers G, Maruhn-Debowski B, März W, Scharf RE. Zotz RB, et al. Among authors: maruhn debowski b. Thromb Haemost. 1998 Apr;79(4):731-5. Thromb Haemost. 1998. PMID: 9569182

8

Genetic typing of human platelet antigen 1 (HPA-1) by oligonucleotide ligation assay in a specific and reliable semi-automated system.

Zotz RB, Giers G, Maruhn-Debowski B, Scharf RE. Zotz RB, et al. Among authors: maruhn debowski b. Br J Haematol. 1997 Jan;96(1):198-203. doi: 10.1046/j.1365-2141.1997.d01-1980.x. Br J Haematol. 1997. PMID: 9012710 Free article.

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