11 Einträge gefunden

1. ITI with high-dose FIX and combined immunosuppressive therapy in a patient with severe haemophilia B and inhibitor.

   1. Beutel, Karin
   2. Hauch, H
   3. Rischewski, J
   4. Kordes, Uwe
   5. Schneppenheim, J
   6. Schneppenheim, Reinhard

   2009 - Forschungsinformationssystem des UKE
2. The problem of novel FVIII missense mutations for haemophilia A genetic counseling.

   1. Schneppenheim, Reinhard
   2. Schröder, J
   3. Obser, Tobias
   4. Oyen, Florian
   5. Schneppenheim, S
   6. Oldenburg, J

   2009 - Forschungsinformationssystem des UKE
3. Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis.

   1. Schneppenheim, Reinhard
   2. Baldauf, C
   3. Stacklies, W
   4. Obser, T
   5. Pieconka, A
   6. Schneppenheim, S
   7. Budde, U

   2009 - Forschungsinformationssystem des UKE
4. 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
5. Acquired von Willebrand syndrome as side effect of valproic acid therapy in children is rare.

   1. Eberl, Wolfgang
   2. Budde, U
   3. Bentele, Karl H. P.
   4. Christen, H-J
   5. Knapp, R
   6. Mey, A
   7. Schneppenheim, Reinhard

   2009 - Forschungsinformationssystem des UKE
6. Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A-TCRAD juxtaposition.

   1. Bug, Stefanie
   2. Dürig, Jan
   3. Oyen, Florian
   4. Klein-Hitpass, Ludger
   5. Martin-Subero, Jose I
   6. Harder, Lana
   7. Baudis, Michael

   2009 - Forschungsinformationssystem des UKE
7. Variations in the ratio between von Willebrand factor and its cleaving protease during systemic inflammation and association with severity and prognosis of organ failure.

   1. Claus, Ralf A
   2. Bockmeyer, Clemens L
   3. Ulrich, Budde
   4. Kentouche, Karim
   5. Sossdorf, Maik
   6. Hilberg, Thomas
   7. Schneppenheim, Reinhard

   2009 - Forschungsinformationssystem des UKE
8. Heterozygous missense protein S mutation in a young boy with incomplete tetraplegia.

   1. Mauz-Koerholz, C
   2. Müller, T
   3. Kunze, C
   4. Schneppenheim, Reinhard
   5. Bernstaedt, M
   6. Koerholz, D

   2009 - Forschungsinformationssystem des UKE
9. Pancytopenia in a 4-year-old boy. 22q11.2 microdeletion syndrome.

   1. Lehmberg, Kai
   2. Rohr, Jan
   3. Schneppenheim, Reinhard
   4. Sommerfeld, Kathrin
   5. Janka-Schaub, Gritta

   2009 - Forschungsinformationssystem des UKE
10. Paediatric haemostaseology.

    1. Schneppenheim, Reinhard

    2009 - Forschungsinformationssystem des UKE
11. A novel type 2A von Willebrand factor mutation (V1499E) associated with variable clinical expression.

    1. van Den, Heuvel
    2. Esther, [Unbekannt]
    3. Laat, de
    4. Bas, [Unbekannt]
    5. Eckmann, [Unbekannt]
    6. Carel, M
    7. Michiels, [Unbekannt]

    2009 - Forschungsinformationssystem des UKE