5 Einträge gefunden

1. Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation

   1. Klemann, Christian
   2. Ammann, Sandra
   3. Heizmann, Miriam
   4. Fuchs, Sebastian
   5. Bode, Sebastian F
   6. Heeg, Maximilian
   7. Fuchs, Hans

   2017 - Forschungsinformationssystem des UKE
2. A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.

   1. Bryceson, Yenan T
   2. Pende, Daniela
   3. Maul-Pavicic, Andrea
   4. Gilmour, Kimberly C
   5. Ufheil, Heike
   6. Vraetz, Thomas
   7. Chiang, Samuel C

   2012 - Forschungsinformationssystem des UKE
3. Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.

   1. Bode, Sebastian Fn
   2. Lehmberg, Kai
   3. Maul-Pavicic, Andrea
   4. Vraetz, Thomas
   5. Janka-Schaub, Gritta
   6. Zur Stadt, Udo
   7. Ehl, Stephan

   2012 - Forschungsinformationssystem des UKE - frei zugänglich
4. 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
5. 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