Facetten
Zugriff
Einrichtung
Medientyp
- Text 7
Karte
Erscheinungsjahr
Autor/in
- Schneppenheim, Reinhard
- Budde, U 3
- Oyen, Florian 3
- Obser, Tobias 2
- Adamtziki, E 1
- alle zeigen
Sprache
7 Einträge gefunden
-
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
2008 - Forschungsinformationssystem des UKE -
Successful donor-lymphocyte infusion for extreme immune-hemolysis following unrelated BMT in a patient with X-linked chronic granulomatous disease and McLeod phenotype.
- Kordes, Uwe
- Binder, Thomas
- Eiermann, Thomas
- Hassenpflug-Diedrich, B
- Hassan, M A
- Beutel, Karin
- Nagy, M
-
-
An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.
2008 - Forschungsinformationssystem des UKE -
-
-
Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor.
- Bockmeyer, Clemens L
- Claus, Ralf A
- Budde, Ulrich
- Kentouche, Karim
- Schneppenheim, Reinhard
- Lösche, Wolfgang
- Reinhart, Konrad