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Autor/in
- Schneppenheim, Sonja
- Schneppenheim, Reinhard 13
- Budde, Ulrich 12
- Obser, Tobias 9
- König, Gesa 4
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16 Einträge gefunden
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Characterization of VWF gene conversions causing von Willebrand disease
- Ahmad, Firdos
- Kannan, Meganathan
- Obser, Tobias
- Budde, Ulrich
- Schneppenheim, Sonja
- Saxena, Renu
- Schneppenheim, Reinhard
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Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging
- Löf, Achim
- König, Gesa
- Schneppenheim, Sonja
- Schneppenheim, Reinhard
- Benoit, Martin
- Budde, Ulrich
- Müller, Jochen P
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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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Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias
- Dicke, Christina
- Schneppenheim, Sonja
- Holstein, Katharina
- Spath, Brigitte
- Bokemeyer, Carsten
- Dittmer, Rita
- Budde, Ulrich
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von Willebrand factor is dimerized by protein disulfide isomerase
- Lippok, Svenja
- Kolšek, Katra
- Löf, Achim
- Eggert, Dennis
- Vanderlinden, Willem
- Müller, Jochen P
- König, Gesa
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Von Willebrand factor regulates complement on endothelial cells
- Noone, Damien G
- Riedl, Magdalena
- Pluthero, Fred G
- Bowman, Mackenzie L
- Liszewski, M Kathryn
- Lu, Lily
- Quan, Yi
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Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus
- Dicke, Christina
- Holstein, Katharina
- Schneppenheim, Sonja
- Dittmer, Rita
- Schneppenheim, Reinhard
- Bokemeyer, Carsten
- Iking-Konert, Christof
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Inherited thrombotic thrombocytopenic purpura in children
2014 - Forschungsinformationssystem des UKE -
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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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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