Nowak-Göttl U - Search Results

1

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.

Bogdanova N, Markoff A, Pollmann H, Nowak-Göttl U, Eisert R, Wermes C, Todorova A, Eigel A, Dworniczak B, Horst J. Bogdanova N, et al. Hum Mutat. 2005 Sep;26(3):249-54. doi: 10.1002/humu.20208. Hum Mutat. 2005. PMID: 16086318

2

Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A.

Bogdanova N, Markoff A, Eisert R, Wermes C, Pollmann H, Todorova A, Chlystun M, Nowak-Göttl U, Horst J. Bogdanova N, et al. Hum Mutat. 2007 Jan;28(1):54-60. doi: 10.1002/humu.20403. Hum Mutat. 2007. PMID: 16972227

3

Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.

Bogdanova N, Markoff A, Pollmann H, Nowak-Göttl U, Eisert R, Dworniczak B, Eigel A, Horst J. Bogdanova N, et al. Hum Mutat. 2002 Sep;20(3):236-7. doi: 10.1002/humu.9062. Hum Mutat. 2002. PMID: 12204009

4

Influence of factor 5 rs6025 and factor 2 rs1799963 mutation on inhibitor development in patients with hemophilia A--an Israeli-German multicenter database study.

Kenet G, Bidlingmaier C, Bogdanova N, Ettingshausen CE, Goldenberg N, Gutsche S, Halimeh S, Holzhauer S, Kurnik K, Limperger V, Junker R, Nowak-Göttl U. Kenet G, et al. Thromb Res. 2014 Apr;133(4):544-9. doi: 10.1016/j.thromres.2014.01.005. Epub 2014 Jan 17. Thromb Res. 2014. PMID: 24485400 Free article.

5

Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors.

Escuriola Ettingshausen C, Halimeh S, Kurnik K, Schobess R, Wermes C, Junker R, Kreuz W, Pollmann H, Nowak-Göttl U. Escuriola Ettingshausen C, et al. Thromb Haemost. 2001 Feb;85(2):218-20. Thromb Haemost. 2001. PMID: 11246535

6

Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a).

Kosch A, Junker R, Wermes C, Nowak-Göttl U. Kosch A, et al. Thromb Res. 2002 Jan 1;105(1):49-53. doi: 10.1016/s0049-3848(01)00406-6. Thromb Res. 2002. PMID: 11864707 Review.

7

Haemophilia and thrombophilia. What do we learn about combined inheritance of both genetic variations?

Nowak-Göttl U, Escuriola C, Kurnik K, Schobess R, Horneff S, Kosch A, Kreuz W, Pollmann H. Nowak-Göttl U, et al. Hamostaseologie. 2003 Feb;23(1):36-40. Hamostaseologie. 2003. PMID: 12567198

8

Lipoprotein (a): its role in childhood thromboembolism.

Nowak-Göttl U, Debus O, Findeisen M, Kassenböhmer R, Koch HG, Pollmann H, Postler C, Weber P, Vielhaber H. Nowak-Göttl U, et al. Pediatrics. 1997 Jun;99(6):E11. doi: 10.1542/peds.99.6.e11. Pediatrics. 1997. PMID: 9164807

9

Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.

Nowak-Göttl U, Wermes C, Junker R, Koch HG, Schobess R, Fleischhack G, Schwabe D, Ehrenforth S. Nowak-Göttl U, et al. Blood. 1999 Mar 1;93(5):1595-9. Blood. 1999. PMID: 10029588 Free article.

10

Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.

Picard V, Nowak-Göttl U, Biron-Andreani C, Fouassier M, Frere C, Goualt-Heilman M, de Maistre E, Regina S, Rugeri L, Ternisien C, Trichet C, Vergnes C, Aiach M, Alhenc-Gelas M. Picard V, et al. Hum Mutat. 2006 Jun;27(6):600. doi: 10.1002/humu.9425. Hum Mutat. 2006. PMID: 16705712

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