7 Einträge gefunden

1. Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.

   1. Castaman, G
   2. Giacomelli, S H
   3. Jacobi, P M
   4. Obser, Tobias
   5. Budde, U
   6. Rodeghiero, F
   7. Schneppenheim, Reinhard

   2012 - Forschungsinformationssystem des UKE
2. Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype.

   1. Castaman, G
   2. Giacomelli, S H
   3. Jacobi, P
   4. Obser, Tobias
   5. Budde, U
   6. Rodeghiero, F
   7. Haberichter, S L

   2010 - Forschungsinformationssystem des UKE
3. Response to DDAVP in children with von Willebrand disease type 2.

   1. Schneppenheim, Reinhard
   2. Budde, U
   3. Beutel, Karin
   4. Hassenpflug, W-A
   5. Hauch, H
   6. Obser, Tobias
   7. Oyen, Florian

   2009 - Forschungsinformationssystem des UKE
4. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.

   1. Gupta, P K
   2. Saxena, R
   3. Adamtziki, E
   4. Budde, U
   5. Oyen, Florian
   6. Obser, Tobias
   7. Schneppenheim, Reinhard

   2008 - Forschungsinformationssystem des UKE
5. Gene conversions are a common cause of von Willebrand disease.

   1. Gupta, P K
   2. Adamtziki, E
   3. Budde, U
   4. Jaiprakash, M
   5. Kumar, H
   6. Harbeck-Seu, A
   7. Kannan, M

   2005 - Forschungsinformationssystem des UKE
6. [Thrombotic thrombocytopenic purpura in childhood]

   1. Hassenpflug, W-A
   2. Angerhaus, D
   3. Budde, U
   4. Obser, Tobias
   5. Schneppenheim, R

   2004 - Forschungsinformationssystem des UKE
7. Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease.

   1. Schneppenheim, R
   2. Budde, U
   3. Obser, Tobias
   4. Brassard, J
   5. Mainusch, K
   6. Ruggeri, Z M
   7. Schneppenheim, S

   2001 - Forschungsinformationssystem des UKE