5 Einträge gefunden

1. Inherited Thrombotic Thrombocytopenic Purpura (Upshaw Schulman Syndrome) as Differential Diagnosis to Neonatal Septicaemia with Disseminated Intravascular Coagulation - a Case Series

   1. Lehmberg, K
   2. Hassenpflug, W A
   3. Klaassen, I
   4. Hillebrand, G
   5. Oyen, F
   6. Budde, U
   7. Singer, D

   2017 - Forschungsinformationssystem des UKE
2. Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami

   1. Obser, T
   2. Ledford-Kraemer, M
   3. Oyen, F
   4. Brehm, M A
   5. Denis, C V
   6. Marschalek, R
   7. Montgomery, R R

   2016 - Forschungsinformationssystem des UKE
3. Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease

   1. Ahmad, F
   2. Oyen, F
   3. Jan, R
   4. Budde, U
   5. Schneppenheim, R
   6. Saxena, R

   2014 - Forschungsinformationssystem des UKE
4. von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor

   1. Brehm, M A
   2. Huck, Volker
   3. Aponte-Santamaría, C
   4. Obser, T
   5. Grässle, S
   6. Oyen, F
   7. Budde, U

   2014 - Forschungsinformationssystem des UKE
5. Thrombotic microangiopathy in a 17-year-old Patient: TTP, HUS or a bit of both?

   1. Gerth, J
   2. Busch, M
   3. Oyen, F
   4. Schneppenheim, R
   5. Keller, T
   6. Budde, U
   7. Groene, H-J

   2007 - Forschungsinformationssystem des UKE