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A common origin of the 4143insA ADAMTS13 mutation.
Schneppenheim R, Kremer Hovinga JA, Becker T, Budde U, Karpman D, Brockhaus W, Hrachovinová I, Korczowski B, Oyen F, Rittich S, von Rosen J, Tjønnfjord GE, Pimanda JE, Wienker TF, Lämmle B. Schneppenheim R, et al. Thromb Haemost. 2006 Jul;96(1):3-6. doi: 10.1160/TH05-12-0817. Thromb Haemost. 2006. PMID: 16807643
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.
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.
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.
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.
253 results