7 Einträge gefunden

1. Differentiating macrophage activation syndrome in systemic juvenile idiopathic arthritis from other forms of hemophagocytic lymphohistiocytosis

   1. Lehmberg, Kai
   2. Pink, Isabell
   3. zu Eulenburg, Christine
   4. Beutel, Karin
   5. Maul-Pavicic, Andrea
   6. Janka-Schaub, Gritta

   2013 - Forschungsinformationssystem des UKE
2. 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
3. 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
4. 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
5. 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
6. 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
7. Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

   1. zur Stadt, Udo
   2. Rohr, Jan
   3. Seifert, Wenke
   4. Koch, Florian
   5. Grieve, Samantha
   6. Pagel, Julia
   7. Strauss, Julia

   2009 - Forschungsinformationssystem des UKE - frei zugänglich