(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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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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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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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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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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Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation von Keles, Sevgi, Charbonnier, Louis Marie, Kabaleeswaran, Venkataraman, Reisli, Ismail, Genel, Ferah, Gulez, Nesrin, Al-Herz, Waleed, Ramesh, Narayanaswamy, Perez-Atayde, Antonio, Karaca, Neslihan E., Kutukculer, Necil, Wu, Hao, Geha, Raif S., Chatila, Talal A.

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Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency von Kiykim, Ayca, Ogulur, Ismail, Dursun, Esra, Charbonnier, Louis Marie, Nain, Ercan, Cekic, Sukru, Dogruel, Dilek, Karaca, Neslihan Edeer, Cogurlu, Mujde Tuba, Bilir, Ozlem Arman, Cansever, Murat, Kapakli, Hasan, Baser, Dilek, Kasap, Nurhan, Kutlug, Seyhan, Altintas, Derya Ufuk, Al-Shaibi, Ahmad, Agrebi, Nourhen, Kara, Manolya, Guven, Ayla, Somer, Ayper, Aydogmus, Cigdem, Ayaz, Nuray Aktay, Metin, Ayse, Aydogan, Metin, Uncuoglu, Aysen, Patiroglu, Turkan, Yildiran, Alisan, Guner, Sukru Nail, Keles, Sevgi, Reisli, Ismail, Aksu, Guzide, Kutukculer, Necil, Kilic, Sara S., Yilmaz, Mustafa, Karakoc-Aydiner, Elif, Lo, Bernice, Ozen, Ahmet, Chatila, Talal A., Baris, Safa

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Type I IFN–related NETosis in ataxia telangiectasia and Artemis deficiency von Gul, Ersin, Sayar, Esra Hazar, Gungor, Bilgi, Eroglu, Fehime Kara, Surucu, Naz, Keles, Sevgi, Guner, Sukru Nail, Findik, Siddika, Alpdundar, Esin, Ayanoglu, Ihsan Cihan, Kayaoglu, Basak, Geckin, Busra Nur, Sanli, Hatice Asena, Kahraman, Tamer, Yakicier, Cengiz, Muftuoglu, Meltem, Oguz, Berna, Cagdas Ayvaz, Deniz Nazire, Gursel, Ihsan, Ozen, Seza, Reisli, Ismail, Gursel, Mayda

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Combined immunodeficiency caused by a loss-of-function mutation in DNA polymerase delta 1 von Cui, Ye, Keles, Sevgi, Charbonnier, Louis-Marie, Julé, Amélie M., Henderson, Lauren, Celik, Seyma Celikbilek, Reisli, Ismail, Shen, Chen, Xie, Wen Jun, Schmitz-Abe, Klaus, Wu, Hao, Chatila, Talal A.

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DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation von Jabara, Haifa H, McDonald, Douglas R, Janssen, Erin, Massaad, Michel J, Ramesh, Narayanaswamy, Borzutzky, Arturo, Rauter, Ingrid, Benson, Halli, Schneider, Lynda, Baxi, Sachin, Recher, Mike, Notarangelo, Luigi D, Wakim, Rima, Dbaibo, Ghassan, Dasouki, Majed, Al-Herz, Waleed, Barlan, Isil, Baris, Safa, Kutukculer, Necil, Ochs, Hans D, Plebani, Alessandro, Kanariou, Maria, Lefranc, Gerard, Reisli, Ismail, Fitzgerald, Katherine A, Golenbock, Douglas, Manis, John, Keles, Sevgi, Ceja, Reuben, Chatila, Talal A, Geha, Raif S

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Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines von Hernandez, Nicholas, Bucciol, Giorgia, Moens, Leen, Le Pen, Jérémie, Shahrooei, Mohammad, Goudouris, Ekaterini, Shirkani, Afshin, Changi-Ashtiani, Majid, Rokni-Zadeh, Hassan, Sayar, Esra Hazar, Reisli, Ismail, Lefevre-Utile, Alain, Zijlmans, Dick, Jurado, Andrea, Pholien, Ruben, Drutman, Scott, Belkaya, Serkan, Cobat, Aurelie, Boudewijns, Robbert, Jochmans, Dirk, Neyts, Johan, Seeleuthner, Yoann, Lorenzo-Diaz, Lazaro, Enemchukwu, Chibuzo, Tietjen, Ian, Hoffmann, Hans-Heinrich, Momenilandi, Mana, Pöyhönen, Laura, Siqueira, Marilda M, de Lima, Sheila M Barbosa, de Souza Matos, Denise C, Homma, Akira, Maia, Maria de Lourdes S, da Costa Barros, Tamiris Azamor, de Oliveira, Patricia Mouta Nunes, Mesquita, Emersom Ciclini, Gijsbers, Rik, Zhang, Shen-Ying, Seligman, Stephen J, Abel, Laurent, Hertzog, Paul, Marr, Nico, Martins, Reinaldo de Menezes, Meyts, Isabelle, Zhang, Qian, MacDonald, Margaret R, Rice, Charles M, Casanova, Jean-Laurent, Jouanguy, Emmanuelle, Bossuyt, Xavier

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F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects von Calzoni, Enrica, Platt, Craig D., Keles, Sevgi, Kuehn, Hye Sun, Beaussant-Cohen, Sarah, Zhang, Yu, Pazmandi, Julia, Lanzi, Gaetana, Pala, Francesca, Tahiat, Azzeddine, Artac, Hasibe, Heredia, Raul Jimenez, Dmytrus, Jasmin, Reisli, Ismail, Uygun, Vedat, Uygun, Dilara, Bingol, Aysen, Basaran, Erdem, Djenouhat, Kamel, Benhalla, Nafissa, Bendahmane, Chafa, Emiroglu, Melike, Kirchhausen, Tomas, Pasham, Mithun, Jones, Jennifer, Wallace, Jacqueline G., Zheng, Lixin, Boisson, Bertrand, Porta, Fulvio, Rosenzweig, Sergio D., Su, Helen, Giliani, Silvia, Lenardo, Michael, Geha, Raif S., Boztug, Kaan, Chou, Janet, Notarangelo, Luigi D.

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An Antibody-Deficiency Syndrome Due to Mutations in the CD19 Gene von van Zelm, Menno C, Reisli, Ismail, van der Burg, Mirjam, Castaño, Diana, van Noesel, Carel J.M, van Tol, Maarten J.D, Woellner, Cristina, Grimbacher, Bodo, Patiño, Pablo J, van Dongen, Jacques J.M, Franco, José L

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