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Characterization of VWF gene conversions causing von Willebrand disease.
Ahmad F, Kannan M, Obser T, Budde U, Schneppenheim S, Saxena R, Schneppenheim R. Ahmad F, et al. Among authors: schneppenheim s, schneppenheim r. Br J Haematol. 2019 Mar;184(5):817-825. doi: 10.1111/bjh.15709. Epub 2018 Nov 29. Br J Haematol. 2019. PMID: 30488424 Free article.
Response to DDAVP in children with von Willebrand disease type 2.
Schneppenheim R, Budde U, Beutel K, Hassenpflug WA, Hauch H, Obser T, Oyen F, Schneppenheim S, Schrum J. Schneppenheim R, et al. Among authors: schneppenheim s. Hamostaseologie. 2009 May;29(2):143-8. Hamostaseologie. 2009. PMID: 19404524
Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami.
Obser T, Ledford-Kraemer M, Oyen F, Brehm MA, Denis CV, Marschalek R, Montgomery RR, Sadler JE, Schneppenheim S, Budde U, Schneppenheim R. Obser T, et al. Among authors: schneppenheim s, schneppenheim r. J Thromb Haemost. 2016 Sep;14(9):1725-35. doi: 10.1111/jth.13398. Epub 2016 Aug 20. J Thromb Haemost. 2016. PMID: 27344059 Free PMC article.
Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient.
Enayat MS, Ravanbod S, Rassoulzadegan M, Jazebi M, Ala F, Budde U, Schneppenheim S, Obser T, Schneppenheim R. Enayat MS, et al. Among authors: schneppenheim s, schneppenheim r. Haemophilia. 2013 Jul;19(4):e261-4. doi: 10.1111/hae.12161. Epub 2013 May 7. Haemophilia. 2013. PMID: 23647747 No abstract available.
38 results