Libyan Boy with Autosomal Recessive Trait (P22-phox Defect) of Chronic Granulomatous Disease

Por Al-Bousafy, Ahmed, Al-Tubuly, Abdulhamid, Dawi, Elhassan, Zaroog, Salem, Schulze, Ilka
Publicado em 2006

Novel cell death program leads to neutrophil extracellular traps

Por Fuchs, Tobias A., Abed, Ulrike, Goosmann, Christian, Hurwitz, Robert, Schulze, Ilka, Wahn, Volker, Weinrauch, Yvette, Brinkmann, Volker, Zychlinsky, Arturo
Publicado em 2007

Myeloperoxidase is required for neutrophil extracellular trap formation: implications for innate immunity

Por Metzler, Kathleen D., Fuchs, Tobias A., Nauseef, William M., Reumaux, Dominique, Roesler, Joachim, Schulze, Ilka, Wahn, Volker, Papayannopoulos, Venizelos, Zychlinsky, Arturo
Publicado em 2011

ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis

Por Maul-Pavicic, Andrea, Chiang, Samuel C. C., Rensing-Ehl, Anne, Jessen, Birthe, Fauriat, Cyril, Wood, Stephanie M., Sjöqvist, Sebastian, Hufnagel, Markus, Schulze, Ilka, Bass, Thilo, Schamel, Wolfgang W., Fuchs, Sebastian, Pircher, Hanspeter, McCarl, Christie-Ann, Mikoshiba, Katsuhiko, Schwarz, Klaus, Feske, Stefan, Bryceson, Yenan T., Ehl, Stephan
Publicado em 2011

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Por Salzer, Ulrich, Bacchelli, Chiara, Buckridge, Sylvie, Pan-Hammarström, Qiang, Jennings, Stephanie, Lougaris, Vassilis, Bergbreiter, Astrid, Hagena, Tina, Birmelin, Jennifer, Plebani, Alessandro, Webster, A. David B., Peter, Hans-Hartmut, Suez, Daniel, Chapel, Helen, McLean-Tooke, Andrew, Spickett, Gavin P., Anover-Sombke, Stephanie, Ochs, Hans D., Urschel, Simon, Belohradsky, Bernd H., Ugrinovic, Sanja, Kumararatne, Dinakantha S., Lawrence, Tatiana C., Holm, Are M., Franco, Jose L., Schulze, Ilka, Schneider, Pascal, Gertz, E. Michael, Schäffer, Alejandro A., Hammarström, Lennart, Thrasher, Adrian J., Gaspar, H. Bobby, Grimbacher, Bodo
Publicado em 2009

Large Deletions and Point Mutations Involving DOCK8 in the Autosomal Recessive Form of the Hyper-IgE Syndrome

Por Engelhardt, Karin R., McGhee, Sean, Winkler, Sabine, Sassi, Atfa, Woellner, Cristina, Lopez-Herrera, Gabriela, Chen, Andrew, Kim, Hong Sook, Lloret, Maria Garcia, Schulze, Ilka, Ehl, Stephan, Thiel, Jens, Pfeifer, Dietmar, Veelken, Hendrik, Niehues, Tim, Siepermann, Kathrin, Weinspach, Sebastian, Reisli, Ismail, Keles, Sevgi, Genel, Ferah, Kütükçüler, Necil, Camcioğlu, Yildiz, Somer, Ayper, Aydiner, Elif Karakoc, Barlan, Isil, Gennery, Andrew, Metin, Ayse, Degerliyurt, Aydan, Pietrogrande, Maria C., Yeganeh, Mehdi, Baz, Zeina, Al-Tamemi, Salem, Klein, Christoph, Puck, Jennifer M., Holland, Steven M., McCabe, Edward R. B., Grimbacher, Bodo, Chatila, Talal
Publicado em 2009

The extended clinical phenotype of 64 patients with DOCK8 deficiency

Por Engelhardt, Karin R., Gertz, E. Michael, Keles, Sevgi, Schäffer, Alejandro A., Sigmund, Elena C., Glocker, Cristina, Saghafi, Shiva, Pourpak, Zahra, Ceja, Ruben, Sassi, Atfa, Graham, Laura E., Massaad, Michel J., Mellouli, Fethi, Ben-Mustapha, Imen, Khemiri, Monia, Kilic, Sara Sebnem, Etzioni, Amos, Freeman, Alexandra F., Thiel, Jens, Schulze, Ilka, Al-Herz, Waleed, Metin, Ayse, Sanal, Özden, Tezcan, Ilhan, Yeganeh, Mehdi, Niehues, Tim, Dueckers, Gregor, Weinspach, Sebastian, Patiroglu, Turkan, Unal, Ekrem, Dasouki, Majed, Yilmaz, Mustafa, Genel, Ferah, Aytekin, Caner, Kutukculer, Necil, Somer, Ayper, Kilic, Mehmet, Reisli, Ismail, Camcioglu, Yildiz, Gennery, Andrew R., Cant, Andrew J., Jones, Alison, Gaspar, H. Bobby, Arkwright, Peter D., Pietrogrande, Maria C., Baz, Zeina, Al-Tamemi, Salem, Lougaris, Vassilios, Lefranc, Gerard, Megarbane, Andre, Boutros, Jeannette, Galal, Nermeen, Bejaoui, Mohamed, Barbouche, Mohamed-Ridha, Geha, Raif S., Chatila, Talal A., Grimbacher, Bodo
Publicado no J Allergy Clin Immunol (2015)