5 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. Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion

   1. Langer, Florian
   2. Obser, Tobias
   3. Oyen, Florian
   4. Spath, Brigitte
   5. Holstein, Katharina
   6. Greinacher, Andreas
   7. White, James G

   2014 - Forschungsinformationssystem des UKE
3. Characterisation of mutations and molecular studies of type 2 von Willebrand disease.

   1. Ahmad, Firdos
   2. Jan, Rifat
   3. Kannan, Meganathan
   4. Obser, Tobias
   5. Hassan, Md Imtaiyaz
   6. Oyen, Florian
   7. Budde, Ulrich

   2013 - Forschungsinformationssystem des UKE
4. Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients

   1. Ahmad, Firdos
   2. Budde, Ulrich
   3. Jan, Rifat
   4. Oyen, Florian
   5. Kannan, Meganathan
   6. Saxena, Renu
   7. Schneppenheim, Reinhard

   2013 - Forschungsinformationssystem des UKE
5. 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