4 Einträge gefunden

1. Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)

   1. Pagel, Julia
   2. Beutel, Karin
   3. Lehmberg, Kai
   4. Koch, Florian
   5. Maul-Pavicic, Andrea
   6. Rohlfs, Anna-Katharina
   7. Al-Jefri, Abdullah

   2012 - Forschungsinformationssystem des UKE
2. Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome.

   1. Jessen, Birthe
   2. Maul-Pavicic, Andrea
   3. Ufheil, Heike
   4. Vraetz, Thomas
   5. Enders, Anselm
   6. Lehmberg, Kai
   7. Längler, Alfred

   2011 - Forschungsinformationssystem des UKE
3. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

   1. Rohr, Jan
   2. Beutel, Karin
   3. Maul-Pavicic, Andrea
   4. Vraetz, Thomas
   5. Thiel, Jens
   6. Warnatz, Klaus
   7. Bondzio, Ilka

   2010 - Forschungsinformationssystem des UKE - frei zugänglich
4. Infection of T lymphocytes in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in children of non-Asian origin.

   1. Beutel, Karin
   2. Gross-Wieltsch, Ute
   3. Wiesel, Thomas
   4. Zur Stadt, Udo
   5. Janka-Schaub, Gritta
   6. Wagner, Hans-Joachim

   2009 - Forschungsinformationssystem des UKE