Is colchicine more effective to prevent periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis episodes in Mediterranean fever gene variants? von Gunes, Muhammed, Cekic, Sukru, Kilic, Sara Sebnem

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Activation-Induced Cytidine Deaminase Expression in Human B Cell Precursors Is Essential for Central B Cell Tolerance von Cantaert, Tineke, Schickel, Jean-Nicolas, Bannock, Jason M., Ng, Yen-Shing, Massad, Christopher, Oe, Tyler, Wu, Renee, Lavoie, Aubert, Walter, Jolan E., Notarangelo, Luigi D., Al-Herz, Waleed, Kilic, Sara Sebnem, Ochs, Hans D., Nonoyama, Shigeaki, Durandy, Anne, Meffre, Eric

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Central control of fever and female body temperature by RANKL/RANK von Ueta, Yoichi, Klaere, Steffen, Hanada, Reiko, Leibbrandt, Andreas, Bader, Michael, Trichereau, Jean, Paolino, Magdalena, Penninger, Josef M, Hanada, Toshikatsu, Kilic, Sara Sebnem, Pifl, Christian, Furuyashiki, Tomoyuki, Qadri, Fatimunnisa, von Haeseler, Arndt, Plehm, Ralph, Komnenovic, Vukoslav, Narumiya, Shuh, Fujihara, Hiroaki, Takahashi, Naoyuki, Kitaoka, Shiho, Mimata, Hiromitsu, Yoshimatsu, Hironobu

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Coexistence of IL12Rβ1 and BTK Mutations in a Family von Kose, Hulya, Gorukmez, Orhan, Kilic, Sara Sebnem

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Editorial: Women in primary immunodeficiencies von Kilic, Sara Sebnem

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Clinical features of children with chronic non-bacterial osteomyelitis: A multicenter retrospective case series from Turkey von Acar?, Ceyhun, Comak, Elif, cekic, Sukru, Turkucar, Serkan, Dundar, Hatice Ad?guzel, K?l?c, Sara Sebnem, Akman, Sema, Makay, Balahan, Unsal, Sevket Erbil

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Neurological involvement in patients with primary immunodeficiency von Kose, Hulya, Karali, Zuhal, Bodur, Muhittin, Cekic, Sukru, Kilic, Sara Sebnem

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Inherited and acquired immunodeficiencies underlying tuberculosis in childhood von Boisson-Dupuis, Stéphanie, Bustamante, Jacinta, El-Baghdadi, Jamila, Camcioglu, Yildiz, Parvaneh, Nima, El Azbaoui, Safaa, Agader, Aomar, Hassani, Amal, El Hafidi, Naima, Mrani, Nidal Alaoui, Jouhadi, Zineb, Ailal, Fatima, Najib, Jilali, Reisli, Ismail, Zamani, Adil, Yosunkaya, Sebnem, Gulle-Girit, Saniye, Yildiran, Alisan, Cipe, Funda Erol, Torun, Selda Hancerli, Metin, Ayse, Atikan, Basak Yildiz, Hatipoglu, Nevin, Aydogmus, Cigdem, Kilic, Sara Sebnem, Dogu, Figen, Karaca, Neslihan, Aksu, Guzide, Kutukculer, Necil, Keser-Emiroglu, Melike, Somer, Ayper, Tanir, Gonul, Aytekin, Caner, Adimi, Parisa, Mahdaviani, Seyed Alireza, Mamishi, Setareh, Bousfiha, Aziz, Sanal, Ozden, Mansouri, Davood, Casanova, Jean-Laurent, Abel, Laurent

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Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+ T cells into distinct effector subsets von Ma, Cindy S, Wong, Natalie, Rao, Geetha, Nguyen, Akira, Avery, Danielle T, Payne, Kathryn, Torpy, James, O'Young, Patrick, Deenick, Elissa, Bustamante, Jacinta, Puel, Anne, Okada, Satoshi, Kobayashi, Masao, Martinez-Barricarte, Ruben, Elliott, Michael, Sebnem Kilic, Sara, El Baghdadi, Jamila, Minegishi, Yoshiyuki, Bousfiha, Aziz, Robertson, Nic, Hambleton, Sophie, Arkwright, Peter D, French, Martyn, Blincoe, Annaliesse K, Hsu, Peter, Campbell, Dianne E, Stormon, Michael O, Wong, Melanie, Adelstein, Stephen, Fulcher, David A, Cook, Matthew C, Stepensky, Polina, Boztug, Kaan, Beier, Rita, Ikincioğullari, Aydan, Ziegler, John B, Gray, Paul, Picard, Capucine, Boisson-Dupuis, Stéphanie, Phan, Tri Giang, Grimbacher, Bodo, Warnatz, Klaus, Holland, Steven M, Uzel, Gulbu, Casanova, Jean-Laurent, Tangye, Stuart G

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Decreased somatic hypermutation induces an impaired peripheral B cell tolerance checkpoint von Cantaert, Tineke, Schickel, Jean-Nicolas, Bannock, Jason M, Ng, Yen-Shing, Massad, Christopher, Delmotte, Fabien R, Yamakawa, Natsuko, Glauzy, Salome, Chamberlain, Nicolas, Kinnunen, Tuure, Menard, Laurence, Lavoie, Aubert, Walter, Jolan E, Notarangelo, Luigi D, Bruneau, Julie, Al-Herz, Waleed, Kilic, Sara Sebnem, Ochs, Hans D, Cunningham-Rundles, Charlotte, van der Burg, Mirjam, Kuijpers, Taco W, Kracker, Sven, Kaneko, Hideo, Sekinaka, Yujin, Nonoyama, Shigeaki, Durandy, Anne, Meffre, Eric

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Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis von Walne, Amanda J, Collopy, Laura, Cardoso, Shirleny, Ellison, Alicia, Plagnol, Vincent, Albayrak, Canan, Albayrak, Davut, Kilic, Sara Sebnem, Patıroglu, Turkan, Akar, Haluk, Godfrey, Keith, Carter, Tina, Marafie, Makia, Vora, Ajay, Sundin, Mikael, Vulliamy, Thomas, Tummala, Hemanth, Dokal, Inderjeet

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Vedolizumab treatment in a patient with X-linked agammaglobulinemia, is it safe and efficient? von Çekiç, Şükrü, Özgür, Taner, Karalı, Yasin, Özkan, Tanju, Kılıç, Sara Şebnem

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Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients von Köker, Mustafa Yavuz, MD, PhD, Camcıoğlu, Yıldız, MD, van Leeuwen, Karin, BSc, Kılıç, Sara Şebnem, MD, Barlan, Işıl, MD, Yılmaz, Mustafa, MD, Metin, Ayşe, MD, PhD, de Boer, Martin, BSc, Avcılar, Hüseyin, MD, PhD, Patıroğlu, Türkan, MD, Yıldıran, Alişan, MD, Yeğin, Olcay, MD, Tezcan, İlhan, MD, PhD, Sanal, Özden, MD, Roos, Dirk, PhD

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High-content cytometry and transcriptomic biomarker profiling of human B-cell activation von Hennig, Christian, MD, Ilginus, Claudia, Boztug, Kaan, MD, Skokowa, Julia, PhD, Marodi, Laszlo, MD, Szaflarska, Anna, MD, Sass, Mareike, Pignata, Claudio, MD, Kilic, Sara Sebnem, MD, Caragol, Isabel, MD, Baumann, Ulrich, MD, Klein, Christoph, MD, Welte, Karl, MD, Hansen, Gesine, MD

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Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome von Mazza, Cinzia, Buzi, Fabio, Ortolani, Federica, Vitali, Alberto, Notarangelo, Lucia D, Weber, Giovanna, Bacchetta, Rosa, Soresina, Annarosa, Lougaris, Vassilios, Greggio, Nella A, Taddio, Andrea, Pasic, Srdjan, de Vroede, Monique, Pac, Malgorzata, Kilic, Sara Sebnem, Ozden, Sanal, Rusconi, Roberto, Martino, Silvana, Capalbo, Donatella, Salerno, Mariacarolina, Pignata, Claudio, Radetti, Giorgio, Maggiore, Giuseppe, Plebani, Alessandro, Notarangelo, Luigi D, Badolato, Raffaele

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From agammaglobulinemia to neutropenia: ‘The TCF‐3 has different clinical presentations’ von Kose, Hulya, Akalin, Akcahan, Kilic, Sara Sebnem

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Can Ikaros mutation lead to intellectual disability? von Kose, Hulya, Kilic, Sara Sebnem

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Infliximab therapy in an infant with Netherton syndrome von Cicek, Fatih, Cekic, Sukru, Kilic, Sara Sebnem

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Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease von Grant, Audrey V, Boisson-Dupuis, Stéphanie, Herquelot, Eléonore, de Beaucoudrey, Ludovic, Filipe-Santos, Orchidée, Nolan, Daniel K, Feinberg, Jacqueline, Boland, Anne, Al-Muhsen, Saleh, Sanal, Ozden, Camcioglu, Yildiz, Palanduz, Ayse, Kilic, Sara Sebnem, Bustamante, Jacinta, Casanova, Jean-Laurent, Abel, Laurent

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Cases with the H syndrome presenting with skin and bone findings von Kose, Hulya, Baskaya, Merve Deniz, Kilic, Sara Sebnem

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