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Autor/in
- Obser, Tobias
- Oyen, Florian
- Schneppenheim, Reinhard 13
- Budde, Ulrich 4
- Budde, U 3
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Sprache
15 Einträge gefunden
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Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany
- Hassenpflug, Wolf Achim
- Obser, Tobias
- Bode, Julia
- Oyen, Florian
- Budde, Ulrich
- Schneppenheim, Sonja
- Schneppenheim, Reinhard
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Platelet-free shear flow assay facilitates analysis of shear-dependent functions of VWF and ADAMTS13
- Kraus, Emma
- Kraus, Kristina
- Obser, Tobias
- Oyen, Florian
- Klemm, Ulrike
- Schneppenheim, Reinhard
- Brehm, Maria A
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Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion
- Langer, Florian
- Obser, Tobias
- Oyen, Florian
- Spath, Brigitte
- Holstein, Katharina
- Greinacher, Andreas
- White, James G
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Characterisation of mutations and molecular studies of type 2 von Willebrand disease.
- Ahmad, Firdos
- Jan, Rifat
- Kannan, Meganathan
- Obser, Tobias
- Hassan, Md Imtaiyaz
- Oyen, Florian
- Budde, Ulrich
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Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression.
- Hasselblatt, Martin
- Gesk, Stefan
- Oyen, Florian
- Rossi, Sabrina
- Viscardi, Elisabetta
- Giangaspero, Felice
- Giannini, Caterina
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A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.
- Schneppenheim, Reinhard
- Michiels, Jan Jacques
- Obser, Tobias
- Oyen, Florian
- Pieconka, Antje
- Schneppenheim, Sonja
- Will, Kerstin
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Response to DDAVP in children with von Willebrand disease type 2.
- Schneppenheim, Reinhard
- Budde, U
- Beutel, Karin
- Hassenpflug, W-A
- Hauch, H
- Obser, Tobias
- Oyen, Florian
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The problem of novel FVIII missense mutations for haemophilia A genetic counseling.
2009 - Forschungsinformationssystem des UKE -
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
2008 - Forschungsinformationssystem des UKE -
An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.
2008 - Forschungsinformationssystem des UKE -
Gene conversions are a common cause of von Willebrand disease.
2005 - Forschungsinformationssystem des UKE -
Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.
- Schneppenheim, Reinhard
- Lenk, Harald
- Obser, Tobias
- Oldenburg, Johannes
- Oyen, Florian
- Schneppenheim, Sonja
- Schwaab, Rainer