5 Einträge gefunden

1. Successful donor-lymphocyte infusion for extreme immune-hemolysis following unrelated BMT in a patient with X-linked chronic granulomatous disease and McLeod phenotype.

   1. Kordes, Uwe
   2. Binder, Thomas
   3. Eiermann, Thomas
   4. Hassenpflug-Diedrich, B
   5. Hassan, M A
   6. Beutel, Karin
   7. Nagy, M

   2008 - Forschungsinformationssystem des UKE
2. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.

   1. Zur Stadt, Udo
   2. Beutel, Karin
   3. Kolberg, Susanne
   4. Schneppenheim, Reinhard
   5. Kabisch, Hartmut
   6. Janka, Gritta
   7. Hennies, Hans Christian

   2006 - Forschungsinformationssystem des UKE
3. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.

   1. Udo, Zur Stadt
   2. Schmidt, Susanne
   3. Kasper, Brigitte
   4. Beutel, Karin
   5. Diler, A Sarper
   6. Henter, Jan-Inge
   7. Kabisch, Hartmut

   2005 - Forschungsinformationssystem des UKE
4. DHPLC based fraction collection of TCR-gamma rearrangements in childhood ALL: direct sequencing of products amplified by a single or a multiplex PCR approach.

   1. Zur Stadt, Udo
   2. Isbarn, Hendrik
   3. Schneppenheim, Reinhard
   4. Kabisch, Hartmut

   2005 - Forschungsinformationssystem des UKE
5. A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.

   1. Udo, Zur Stadt
   2. Beutel, Karin
   3. Weber, Belinda
   4. Kabisch, Hartmut
   5. Schneppenheim, Reinhard
   6. Janka-Schaub, Gritta

   2004 - Forschungsinformationssystem des UKE