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Autor/in
- Kabisch, Hartmut
- Schneppenheim, Reinhard
- Beutel, Karin 4
- Hennies, Hans Christian 2
- Janka-Schaub, Gritta 2
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5 Einträge gefunden
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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
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Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
- Zur Stadt, Udo
- Beutel, Karin
- Kolberg, Susanne
- Schneppenheim, Reinhard
- Kabisch, Hartmut
- Janka, Gritta
- Hennies, Hans Christian
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A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.
- Udo, Zur Stadt
- Beutel, Karin
- Weber, Belinda
- Kabisch, Hartmut
- Schneppenheim, Reinhard
- Janka-Schaub, Gritta