Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia

Por Leuzzi, Vincenzo, Micheli, Roberto, D'Agnano, Daniela, Molinaro, Anna, Venturi, Tullia, Plebani, Alessandro, Soresina, Annarosa, Marini, Mirella, Ferremi Leali, Pierino, Quinti, Isabella, Pietrogrande, Maria C., Finocchi, Andrea, Fazzi, Elisa, Chessa, Luciana, Magnani, Mauro
Publicado no Neurol Neuroimmunol Neuroinflamm (2015)

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

Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome

Por Woellner, Cristina, Gertz, E. Michael, Schäffer, Alejandro A., Lagos, Macarena, Perro, Mario, Glocker, Erik-Oliver, Pietrogrande, Maria C., Cossu, Fausto, Franco, José L., Matamoros, Nuria, Pietrucha, Barbara, Heropolitańska-Pliszka, Edyta, Yeganeh, Mehdi, Moin, Mostafa, Español, Teresa, Ehl, Stephan, Gennery, Andrew R., Abinun, Mario, Bręborowicz, Anna, Niehues, Tim, Kilic, Sara Sebnem, Junker, Anne, Turvey, Stuart E., Plebani, Alessandro, Sánchez, Berta, Garty, Ben-Zion, Pignata, Claudio, Cancrini, Caterina, Litzman, Jiri, Sanal, Özden, Baumann, Ulrich, Bacchetta, Rosa, Hsu, Amy P., Davis, Joie N., Hammarström, Lennart, Davies, E. Graham, Eren, Efrem, Arkwright, Peter D., Moilanen, Jukka S., Viemann, Dorothee, Khan, Sujoy, Maródi, László, Cant, Andrew J., Freeman, Alexandra F., Puck, Jennifer M., Holland, Steven M., Grimbacher, Bodo
Publicado em 2010

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)