Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

Por Rohr, Jan, Beutel, Karin, Maul-Pavicic, Andrea, Vraetz, Thomas, Thiel, Jens, Warnatz, Klaus, Bondzio, Ilka, Gross-Wieltsch, Ute, Schündeln, Michael, Schütz, Barbara, Woessmann, Wilhelm, Groll, Andreas H., Strahm, Brigitte, Pagel, Julia, Speckmann, Carsten, Janka, Gritta, Griffiths, Gillian, Schwarz, Klaus, zur Stadt, Udo, Ehl, Stephan
Publicado em 2010

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

Por Bode, Sebastian FN, Ammann, Sandra, Al-Herz, Waleed, Bataneant, Mihaela, Dvorak, Christopher C, Gehring, Stephan, Gennery, Andrew, Gilmour, Kimberly C, Gonzalez-Granado, Luis I, Groß-Wieltsch, Ute, Ifversen, Marianne, Lingman-Framme, Jenny, Matthes-Martin, Susanne, Mesters, Rolf, Meyts, Isabelle, van Montfrans, Joris M, Schmid, Jana Pachlopnik, Pai, Sung-Yun, Soler-Palacin, Pere, Schuermann, Uta, Schuster, Volker, Seidel, Markus G., Speckmann, Carsten, Stepensky, Polina, Sykora, Karl-Walter, Tesi, Bianca, Vraetz, Thomas, Waruiru, Catherine, Bryceson, Yenan T., Moshous, Despina, Lehmberg, Kai, Jordan, Michael B, Ehl, Stephan
Publicado no Haematologica (2015)