Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome von Engelhardt, Karin R., Dr, McGhee, Sean, MD, Winkler, Sabine, MSc, Sassi, Atfa, PhD, Woellner, Cristina, MSc, Lopez-Herrera, Gabriela, PhD, Chen, Andrew, Kim, Hong Sook, PhD, Lloret, Maria Garcia, MD, Schulze, Ilka, MD, Ehl, Stephan, MD, Thiel, Jens, MD, Pfeifer, Dietmar, Dr, Veelken, Hendrik, MD, Niehues, Tim, MD, Siepermann, Kathrin, MD, Weinspach, Sebastian, MD, Reisli, Ismail, MD, Keles, Sevgi, MD, Genel, Ferah, MD, Kutuculer, Necil, MD, Camcoğlu, Yldz, MD, Somer, Ayper, MD, Karakoc-Aydiner, Elif, MD, Barlan, Isil, MD, Gennery, Andrew, MD, Metin, Ayse, MD, PhD, Degerliyurt, Aydan, MD, Pietrogrande, Maria C., MD, Yeganeh, Mehdi, MD, Baz, Zeina, MD, Al-Tamemi, Salem, MD, Klein, Christoph, MD, PhD, Puck, Jennifer M., MD, Holland, Steven M., MD, McCabe, Edward R.B., MD, PhD, Grimbacher, Bodo, MD, Chatila, Talal A., MD, MSc

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The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency von Engelhardt, Karin R., PhD, Gertz, Michael E., PhD, Keles, Sevgi, MD, Schäffer, Alejandro A., PhD, Sigmund, Elena C., BSc, Glocker, Cristina, PhD, Saghafi, Shiva, MSc, Pourpak, Zahra, MD, PhD, Ceja, Ruben, MSc, Sassi, Atfa, PhD, Graham, Laura E., BSc, MBChB, Massaad, Michel J., PhD, Mellouli, Fethi, MD, Ben-Mustapha, Imen, MD, Khemiri, Monia, MD, Kilic, Sara Sebnem, MD, Etzioni, Amos, MD, Freeman, Alexandra F., MD, Thiel, Jens, MD, Schulze, Ilka, MD, Al-Herz, Waleed, MD, Metin, Ayse, MD, PhD, Sanal, Özden, MD, Tezcan, Ilhan, MD, Yeganeh, Mehdi, MD, Niehues, Tim, MD, Dueckers, Gregor, MD, Weinspach, Sebastian, MD, Patiroglu, Turkan, MD, Unal, Ekrem, MD, Dasouki, Majed, MD, Yilmaz, Mustafa, MD, Genel, Ferah, MD, Aytekin, Caner, MD, Kutukculer, Necil, MD, Somer, Ayper, MD, Kilic, Mehmet, MD, Reisli, Ismail, MD, Camcioglu, Yildiz, MD, Gennery, Andrew R., MD, Cant, Andrew J., MD, Jones, Alison, MD, Gaspar, Bobby H., MD, Arkwright, Peter D., MD, DPhil, Pietrogrande, Maria C., MD, Baz, Zeina, MD, Al-Tamemi, Salem, MD, Lougaris, Vassilios, MD, Lefranc, Gerard, PhD, Megarbane, Andre, MD, PhD, Boutros, Jeannette, MD, Galal, Nermeen, MD, Bejaoui, Mohamed, MD, Barbouche, Mohamed-Ridha, MD, PhD, Geha, Raif S., MD, Chatila, Talal A., MD, MSc, Grimbacher, Bodo, MD

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CD19 controls Toll-like receptor 9 responses in human B cells von Morbach, Henner, MD, Schickel, Jean-Nicolas, PhD, Cunningham-Rundles, Charlotte, MD, PhD, Conley, Mary Ellen, MD, Reisli, Ismail, MD, Franco, Jose Luis, MD, PhD, Meffre, Eric, PhD

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Functional analysis of naturally occurring DCLRE1C mutations and correlation with the clinical phenotype of ARTEMIS deficiency von Felgentreff, Kerstin, MD, Lee, Yu Nee, PhD, Frugoni, Francesco, PhD, Du, Likun, PhD, van der Burg, Mirjam, PhD, Giliani, Silvia, PhD, Tezcan, Ilhan, MD, Reisli, Ismail, MD, Mejstrikova, Ester, MD, de Villartay, Jean-Pierre, PhD, Sleckman, Barry P., MD, PhD, Manis, John, MD, PhD, Notarangelo, Luigi D., MD

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Plasmacytoid dendritic cell depletion in DOCK8 deficiency: Rescue of severe herpetic infections with IFN-α 2b therapy von Keles, Sevgi, MD, Jabara, Haifa H., BSc, Reisli, Ismail, MD, McDonald, Douglas R., MD, PhD, Barlan, Isil, MD, Hanna-Wakim, Rima, MD, Dbaibo, Ghassan, MD, Lefranc, Gerard, PhD, Al-Herz, Waleed, MD, Geha, Raif S., MD, Chatila, Talal A., MD, MSc

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Human CD19 and CD40L deficiencies impair antibody selection and differentially affect somatic hypermutation von van Zelm, Menno C., PhD, Bartol, Sophinus J.W., BSc, Driessen, Gertjan J., MD, PhD, Mascart, Françoise, MD, PhD, Reisli, Ismail, MD, Franco, Jose L., MD, Wolska-Kusnierz, Beata, MD, Kanegane, Hirokazu, MD, PhD, Boon, Louis, PhD, van Dongen, Jacques J.M., MD, PhD, van der Burg, Mirjam, PhD

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How effective are the 6 European Society of Immunodeficiency warning signs for primary immunodeficiency disease? von Arslan, Sevket, MD, Ucar, Ramazan, MD, Caliskaner, Ahmet Zafer, MD, PROF, Reisli, Ismail, MD, PROF, Guner, Sukru Nail, MD, Sayar, Esra Hazar, MD, Baloglu, Ismail, MD

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Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH 17 cell differentiation von Keles, Sevgi, MD, Charbonnier, Louis Marie, PhD, Kabaleeswaran, Venkataraman, PhD, Reisli, Ismail, MD, Genel, Ferah, MD, Gulez, Nesrin, MD, Al-Herz, Waleed, MD, Ramesh, Narayanaswamy, PhD, Perez-Atayde, Antonio, MD, Eeder, Neslihan Karaca, MD, Kutukculer, Necil, MD, Wu, Hao, PhD, Geha, Raif S., MD, Chatila, Talal A., MD, MSc

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Predicting Hospitalization in Children with Acute Asthma von Buyuktiryaki, A. Betul, MD, Civelek, Ersoy, MD, Can, Demet, MD, Orhan, Fazl, MD, Aydogan, Metin, MD, Reisli, Ismail, MD, Keskin, Ozlem, MD, Akcay, Ahmet, MD, Yazicioglu, Mehtap, MD, Cokugras, Haluk, MD, Yuksel, Hasan, MD, Zeyrek, Dost, MD, Kocak, A. Kadir, MD, Sekerel, Bulent E., MD

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Defects along the TH 17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome von Al Khatib, Shadi, MD, Keles, Sevgi, MD, Garcia-Lloret, Maria, MD, Karakoc-Aydiner, Elif, MD, Reisli, Ismail, MD, Artac, Hasibe, MD, Camcioglu, Yildiz, MD, Cokugras, Haluk, MD, Somer, Ayper, MD, Kutukculer, Necil, MD, Yilmaz, Mustafa, MD, Ikinciogullari, Aydan, MD, Yegin, Olcay, MD, Yüksek, Mutlu, MD, Genel, Ferah, MD, Kucukosmanoglu, Ercan, MD, Baki, Ali, MD, Bahceciler, Nerin N., MD, Rambhatla, Anupama, Nickerson, Derek W., BS, McGhee, Sean, MD, Barlan, Isil B., MD, Chatila, Talal, MD, MSc

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(Un)Awareness of allergy von Kalpaklioglu, A Fusun, Kalkan, Ilkay Koca, Akcay, Ahmet, Reisli, Ismail, Can, Demet, Uzuner, Nevin, Yuksel, Hasan, Kirmaz, Cengiz, Gulen, Figen, Ediger, Dane

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Evaluation of the Children with Recurrent Respiratory Tract Infections von Bozdogan, MD. Gunseli, Reisli, MD. Ismail, Dogu, MD. Figen, Ikinciogul, MD. Aydan, Babacan, MD. Emel

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