Search Results - "Bondzio, I"

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency by Rensing-Ehl, A, Warnatz, K, Fuchs, S, Schlesier, M, Salzer, U, Draeger, R, Bondzio, I, Joos, Y, Janda, A, Gomes, M, Abinun, M, Hambleton, S, Cant, A, Shackley, F, Flood, T, Waruiru, C, Beutel, K, Siepermann, K, Dueckers, G, Niehues, T, Wiesel, T, Schuster, V, Seidel, M.G, Minkov, M, Sirkiä, K, Kopp, M.V, Korhonen, M, Schwarz, K, Ehl, S, Speckmann, C

“…Abstract Autoimmune lymphoproliferative syndrome (ALPS) is mainly caused by defects in the CD95 pathway. Raised CD3+TCRαβ+CD4−CD8− double negative T cells and…”
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A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes by Bryceson, Yenan T., Pende, Daniela, Maul-Pavicic, Andrea, Gilmour, Kimberly C., Ufheil, Heike, Vraetz, Thomas, Chiang, Samuel C., Marcenaro, Stefania, Meazza, Raffaella, Bondzio, Ilka, Walshe, Denise, Janka, Gritta, Lehmberg, Kai, Beutel, Karin, zur Stadt, Udo, Binder, Nadine, Arico, Maurizio, Moretta, Lorenzo, Henter, Jan-Inge, Ehl, Stephan

“…Familial hemophagocytic lymphohistiocytosis (FHL) is a life-threatening disorder of immune regulation caused by defects in lymphocyte cytotoxicity. Rapid…”
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Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases by ROHR, Jan, BEUTEL, Karin, WOESSMANN, Wilhelm, GROLL, Andreas H, STRAHM, Brigitte, PAGEL, Julia, SPECKMANN, Carsten, JANKA, Gritta, GRIFFITHS, Gillian, SCHWARZ, Klaus, ZUR STADT, Udo, EHL, Stephan, MAUL-PAVICIC, Andrea, VRAETZ, Thomas, THIEL, Jens, WARNATZ, Klaus, BONDZIO, Ilka, GROSS-WIELTSCH, Ute, SCHÜNDELN, Michael, SCHÜTZ, Barbara

“…Familial hemophagocytic lymphohistiocytosis is a genetic disorder of lymphocyte cytotoxicity that usually presents in the first two years of life and has a…”
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