Schneppenheim R - Search Results

1

Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.

Wetzstein V, Budde U, Oyen F, Ding X, Herrmann J, Liebig B, Schneppenheim R. Wetzstein V, et al. Among authors: schneppenheim r. Haematologica. 2006 Dec;91(12 Suppl):ECR60. Haematologica. 2006. PMID: 17194666

2

Laboratory diagnosis of congenital von Willebrand disease.

Budde U, Drewke E, Mainusch K, Schneppenheim R. Budde U, et al. Among authors: schneppenheim r. Semin Thromb Hemost. 2002 Apr;28(2):173-90. doi: 10.1055/s-2002-27820. Semin Thromb Hemost. 2002. PMID: 11992241 Review.

3

von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.

Schneppenheim R, Budde U, Oyen F, Angerhaus D, Aumann V, Drewke E, Hassenpflug W, Häberle J, Kentouche K, Kohne E, Kurnik K, Mueller-Wiefel D, Obser T, Santer R, Sykora KW. Schneppenheim R, et al. Blood. 2003 Mar 1;101(5):1845-50. doi: 10.1182/blood-2002-08-2399. Epub 2002 Oct 17. Blood. 2003. PMID: 12393505 Free article.

4

Severe ADAMTS-13 deficiency in childhood.

Schneppenheim R, Budde U, Hassenpflug W, Obser T. Schneppenheim R, et al. Semin Hematol. 2004 Jan;41(1):83-9. doi: 10.1053/j.seminhematol.2003.10.007. Semin Hematol. 2004. PMID: 14727263 Review.

5

Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.

Schneppenheim R, Lenk H, Obser T, Oldenburg J, Oyen F, Schneppenheim S, Schwaab R, Will K, Budde U. Schneppenheim R, et al. Among authors: schneppenheim s. Thromb Haemost. 2004 Jul;92(1):36-41. doi: 10.1160/TH04-02-0084. Thromb Haemost. 2004. PMID: 15213842

6

Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS).

Licht C, Stapenhorst L, Simon T, Budde U, Schneppenheim R, Hoppe B. Licht C, et al. Among authors: schneppenheim r. Kidney Int. 2004 Sep;66(3):955-8. doi: 10.1111/j.1523-1755.2004.00841.x. Kidney Int. 2004. PMID: 15327386 Free article.

7

Phenotypic and genotypic diagnosis of von Willebrand disease: a 2004 update.

Schneppenheim R, Budde U. Schneppenheim R, et al. Semin Hematol. 2005 Jan;42(1):15-28. doi: 10.1053/j.seminhematol.2004.10.002. Semin Hematol. 2005. PMID: 15662612 Review.

8

The evolving classification of von Willebrand disease.

Schneppenheim R. Schneppenheim R. Blood Coagul Fibrinolysis. 2005 Apr;16 Suppl 1:S3-S10. doi: 10.1097/01.mbc.0000167656.77520.bb. Blood Coagul Fibrinolysis. 2005. PMID: 15849525 Review.

9

Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis.

Hassenpflug WA, Budde U, Obser T, Angerhaus D, Drewke E, Schneppenheim S, Schneppenheim R. Hassenpflug WA, et al. Among authors: schneppenheim s, schneppenheim r. Blood. 2006 Mar 15;107(6):2339-45. doi: 10.1182/blood-2005-04-1758. Epub 2005 Dec 1. Blood. 2006. PMID: 16322474 Free article.

10

von Willebrand factor-cleaving protease (ADAMTS13) in the course of stem cell transplantation.

Kentouche K, Zintl F, Angerhaus D, Fuchs D, Hermann J, Schneppenheim R, Budde U. Kentouche K, et al. Among authors: schneppenheim r. Semin Thromb Hemost. 2006 Mar;32(2):98-104. doi: 10.1055/s-2006-939765. Semin Thromb Hemost. 2006. PMID: 16575684

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