3 Einträge gefunden

1. Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany

   1. Hassenpflug, Wolf Achim
   2. Obser, Tobias
   3. Bode, Julia
   4. Oyen, Florian
   5. Budde, Ulrich
   6. Schneppenheim, Sonja
   7. Schneppenheim, Reinhard

   2018 - Forschungsinformationssystem des UKE
2. A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.

   1. Schneppenheim, Reinhard
   2. Michiels, Jan Jacques
   3. Obser, Tobias
   4. Oyen, Florian
   5. Pieconka, Antje
   6. Schneppenheim, Sonja
   7. Will, Kerstin

   2010 - Forschungsinformationssystem des UKE
3. Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.

   1. Schneppenheim, Reinhard
   2. Lenk, Harald
   3. Obser, Tobias
   4. Oldenburg, Johannes
   5. Oyen, Florian
   6. Schneppenheim, Sonja
   7. Schwaab, Rainer

   2004 - Forschungsinformationssystem des UKE