42 Einträge gefunden

1. Unterarmgangrän bei "normaler" Gerinnung.

   1. Blohm, Martin
   2. Lehmberg, Kai
   3. Schrum, Johanna
   4. Helmke, Knut
   5. Ridderbusch, Ina
   6. Schneppenheim, Reinhard
   7. Singer, Dominique

   2016 - Forschungsinformationssystem des UKE
2. [Von Willebrand factor and ADAMTS13 balancing primary haemostasis].

   1. Schneppenheim, Reinhard
   2. Budde, U

   2011 - Forschungsinformationssystem des UKE
3. The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.

   1. Haberichter, Sandra L
   2. Ulrich, Budde
   3. Obser, Tobias
   4. Schneppenheim, Sonja
   5. Wermes, Cornelia
   6. Schneppenheim, Reinhard

   2010 - Forschungsinformationssystem des UKE
4. Using ImageJ for the quantitative analysis of flow-based adhesion assays in real-time under physiologic flow conditions.

   1. Sascha, Meyer Dos Santos
   2. Klinkhardt, Ute
   3. Schneppenheim, Reinhard
   4. Harder, Sebastian

   2010 - Forschungsinformationssystem des UKE
5. 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
6. Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD.

   1. Castaman, G
   2. Tosetto, A
   3. Cappelletti, A
   4. Goodeve, A
   5. Federici, A B
   6. Batlle, J
   7. Meyer, D

   2010 - Forschungsinformationssystem des UKE
7. Severe bleeding diathesis associated with moderate thrombocytopenia - diagnostic workup of seven family members with type 2B von Willebrand's disease.

   1. Zdziarska, J
   2. Iwaniec, T
   3. Skotnicki, A B
   4. Musia, J
   5. Schneppenheim, Reinhard
   6. Budde, U
   7. Kentouche, K

   2010 - Forschungsinformationssystem des UKE
8. Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.

   1. Klukowska, Anna
   2. Niewiadomska, Edyta
   3. Ulrich, Budde
   4. Oyen, Florian
   5. Schneppenheim, Reinhard

   2010 - Forschungsinformationssystem des UKE
9. Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.

   1. Schneppenheim, Reinhard
   2. Frühwald, Michael C
   3. Gesk, Stefan
   4. Hasselblatt, Martin
   5. Jeibmann, Astrid
   6. Kordes, Uwe
   7. Kreuz, Markus

   2010 - Forschungsinformationssystem des UKE
10. Loss of SMARCB1/INI1 expression in poorly differentiated chordomas.

    1. Mobley, Bret C
    2. McKenney, Jesse K
    3. Bangs, Charles D
    4. Callahan, Katherine
    5. Yeom, Kristen W
    6. Schneppenheim, Reinhard
    7. Hayden, Melanie G

    2010 - Forschungsinformationssystem des UKE
11. Laboratory diagnosis of von Willebrand disease.

    1. Patzke, J
    2. Schneppenheim, Reinhard

    2010 - Forschungsinformationssystem des UKE
12. Neonatal cholestasis in glucose-6-phosphate dehydrogenase deficiency.

    1. Kordes, Uwe
    2. Briem-Richter, Andrea
    3. Santer, René
    4. Schäfer, Hansjörg
    5. Singer, Dominique
    6. Sonntag, J
    7. Steuerwald, U

    2010 - Forschungsinformationssystem des UKE
13. Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.

    1. Kordes, Uwe
    2. Briem-Richter, Andrea
    3. Santer, René
    4. Schäfer, Hansjörg
    5. Singer, Dominique
    6. Sonntag, Josef
    7. Steuerwald, Ulrike

    2010 - Forschungsinformationssystem des UKE
14. 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
15. 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
16. 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
17. 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
18. 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
19. 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
20. 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