Defective kinase activity of IKKα leads to combined immunodeficiency and disruption of immune tolerance in humans von Cildir, Gökhan, Aba, Umran, Pehlivan, Damla, Tvorogov, Denis, Warnock, Nicholas I., Ipsir, Canberk, Arik, Elif, Kok, Chung Hoow, Bozkurt, Ceren, Tekeoglu, Sidem, Inal, Gaye, Cesur, Mahmut, Kucukosmanoglu, Ercan, Karahan, Ibrahim, Savas, Berna, Balci, Deniz, Yaman, Ayhan, Demirbaş, Nazli Deveci, Tezcan, Ilhan, Haskologlu, Sule, Dogu, Figen, Ikinciogulları, Aydan, Keskin, Ozlem, Tumes, Damon J., Erman, Baran

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Lymphoma Secondary to Congenital and Acquired Immunodeficiency Syndromes at a Turkish Pediatric Oncology Center von Tanyildiz, Hikmet G., Dincaslan, Handan, Yavuz, Gulsan, Unal, Emel, Ikinciogulları, Aydan, Dogu, Figen, Tacyildiz, Nurdan

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Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score von Tesch, Victoria Katharina, Abolhassani, Hassan, Shadur, Bella, Zobel, Joachim, Mareika, Yuliya, Sharapova, Svetlana, Karakoc-Aydiner, Elif, Rivière, Jacques G., Garcia-Prat, Marina, Moes, Nicolette, Haerynck, Filomeen, Gonzales-Granado, Luis I., Santos Pérez, Juan Luis, Mukhina, Anna, Shcherbina, Anna, Aghamohammadi, Asghar, Hammarström, Lennart, Dogu, Figen, Haskologlu, Sule, İkincioğulları, Aydan İ., Köstel Bal, Sevgi, Baris, Safa, Kilic, Sara Sebnem, Karaca, Neslihan Edeer, Kutukculer, Necil, Girschick, Hermann, Kolios, Antonios, Keles, Sevgi, Uygun, Vedat, Stepensky, Polina, Worth, Austen, van Montfrans, Joris M., Peters, Anke M.J., Meyts, Isabelle, Adeli, Mehdi, Marzollo, Antonio, Padem, Nurcicek, Khojah, Amer M., Chavoshzadeh, Zahra, Avbelj Stefanija, Magdalena, Bakhtiar, Shahrzad, Florkin, Benoit, Meeths, Marie, Gamez, Laura, Grimbacher, Bodo, Seppänen, Mikko R.J., Lankester, Arjan, Gennery, Andrew R., Seidel, Markus G.

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Early-onset inflammatory bowel disease and common variable immunodeficiency–like disease caused by IL-21 deficiency von Salzer, Elisabeth, MD, Kansu, Aydan, MD, Sic, Heiko, PhD, Májek, Peter, PhD, Ikincioğullari, Aydan, MD, Dogu, Figen E., MD, Prengemann, Nina Kathrin, MSc, Santos-Valente, Elisangela, MD, MSc, Pickl, Winfried F., PhD, Bilic, Ivan, PhD, Ban, Sol A, Kuloğlu, Zarife, MD, Demir, Arzu Meltem, MD, Ensari, Arzu, MD, Colinge, Jacques, PhD, Rizzi, Marta, PhD, Eibel, Hermann, PhD, Boztug, Kaan, MD

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Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child von Ogishi, Masato, Yang, Rui, Aytekin, Caner, Langlais, David, Bourgey, Mathieu, Khan, Taushif, Ali, Fatima Al, Rahman, Mahbuba, Delmonte, Ottavia M., Chrabieh, Maya, Zhang, Peng, Gruber, Conor, Pelham, Simon J., Spaan, András N., Rosain, Jérémie, Lei, Wei-Te, Drutman, Scott, Hellmann, Matthew D., Callahan, Margaret K., Adamow, Matthew, Wong, Phillip, Wolchok, Jedd D., Rao, Geetha, Ma, Cindy S., Nakajima, Yuka, Yaguchi, Tomonori, Chamoto, Kenji, Williams, Samuel C., Emile, Jean-Francois, Rozenberg, Flore, Glickman, Michael S., Rapaport, Franck, Kerner, Gaspard, Allington, Garrett, Tezcan, Ilhan, Cagdas, Deniz, Hosnut, Ferda O., Dogu, Figen, Ikinciogullari, Aydan, Rao, V. Koneti, Kainulainen, Leena, Béziat, Vivien, Bustamante, Jacinta, Vilarinho, Silvia, Lifton, Richard P., Boisson, Bertrand, Abel, Laurent, Bogunovic, Dusan, Marr, Nico, Notarangelo, Luigi D., Tangye, Stuart G., Honjo, Tasuku, Gros, Philippe, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent

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Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency von Ouederni, Monia, Sanal, Ozden, Ikincioğullari, Aydan, Tezcan, Ilhan, Dogu, Figen, Sologuren, Ithaisa, Pedraza-Sánchez, Sigifredo, Keser, Melike, Tanir, Gonul, Nieuwhof, Chris, Colino, Elena, Kumararatne, Dinakantha, Levy, Jacov, Kutukculer, Necil, Aytekin, Caner, Herrera-Ramos, Estefanía, Bhatti, Micah, Karaca, Neslihan, Barbouche, Ridha, Broides, Arnon, Goudouris, Ekaterini, Franco, José Luis, Parvaneh, Nima, Reisli, Ismail, Strickler, Alexis, Shcherbina, Anna, Somer, Ayper, Segal, Anthony, Angel-Moreno, Alfonso, Lezana-Fernandez, José Luis, Bejaoui, Mohamed, Valle, Miriam Bobadilla-Del, Kachboura, Salem, Sentongo, Timothy, Ben-Mustapha, Imen, Bustamante, Jacinta, Picard, Capucine, Puel, Anne, Boisson-Dupuis, Stéphanie, Abel, Laurent, Casanova, Jean-Laurent, Rodríguez-Gallego, Carlos

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Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation von Seidel, Markus G., MD, Böhm, Katrin, Cm, Dogu, Figen, MD, Worth, Austen, MD, Thrasher, Adrian, MD, Florkin, Benoit, MD, İkincioğulları, Aydan, MD, Peters, Anke, MD, Bakhtiar, Shahrzad, MD, Meeths, Marie, MD, Stepensky, Polina, MD, Meyts, Isabelle, MD, Sharapova, Svetlana O., MD, Gámez-Díaz, Laura, PhD, Hammarström, Lennart, MD, Ehl, Stephan, MD, Grimbacher, Bodo, MD, Gennery, Andrew R., MD

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Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections von Dobbs, Kerry, Domínguez Conde, Cecilia, Zhang, Shen-Ying, Parolini, Silvia, Audry, Magali, Chou, Janet, Haapaniemi, Emma, Keles, Sevgi, Bilic, Ivan, Okada, Satoshi, Massaad, Michel J, Rounioja, Samuli, Alwahadneh, Adel M, Serwas, Nina K, Capuder, Kelly, Çiftçi, Ergin, Felgentreff, Kerstin, Ohsumi, Toshiro K, Pedergnana, Vincent, Boisson, Bertrand, Haskoloğlu, Şule, Ensari, Arzu, Schuster, Michael, Moretta, Alessandro, Itan, Yuval, Patrizi, Ornella, Rozenberg, Flore, Lebon, Pierre, Saarela, Janna, Knip, Mikael, Petrovski, Slavé, Goldstein, David B, Parrott, Roberta E, Savas, Berna, Schambach, Axel, Tabellini, Giovanna, Bock, Christoph, Chatila, Talal A, Comeau, Anne Marie, Geha, Raif S, Abel, Laurent, Buckley, Rebecca H, İkincioğulları, Aydan, Al-Herz, Waleed, Helminen, Merja, Doğu, Figen, Casanova, Jean-Laurent, Boztuğ, Kaan, Notarangelo, Luigi D

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Normal mean platelet volume and thrombocytopenia: It may still be Wiskott–Aldrich syndrome von Haskoloğlu, Şule, Öztürk, Gökcan, Baskın, Kübra, İslamoğlu, Candan, Doğu, Figen, İkincioğulları, Aydan

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Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity von Willmann, Katharina L., Klaver, Stefanie, Doğu, Figen, Santos-Valente, Elisangela, Garncarz, Wojciech, Bilic, Ivan, Mace, Emily, Salzer, Elisabeth, Domínguez Conde, Cecilia, Sic, Heiko, Májek, Peter, Banerjee, Pinaki P., Vladimer, Gregory I., Haskoloğlu, Şule, Gökalp Bolkent, Musa, Küpesiz, Alphan, Condino-Neto, Antonio, Colinge, Jacques, Superti-Furga, Giulio, Pickl, Winfried F., van Zelm, Menno C., Eibel, Hermann, Orange, Jordan S., Ikincioğulları, Aydan, Boztuğ, Kaan

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Very-early-onset Inflammatory Bowel Disease in an Infant with a Partial RIPK1 Deletion von Tuna Kırsaçlıoğlu, Ceyda, Frohne, Alexandra, Kuloğlu, Zarife, Kristofersdottir, Isidora, Demir, Engin, Altuntaş, Cansu, Haskoloğlu, Zehra Şule, Çobanoğlu, Fatma Nazan, Kendirli, Tanıl, Özdemir, Halil, Özçakar, Zeynep Birsin, Savaş, Berna, Doğu, Figen, İkincioğulları, Aydan, Boztug, Kaan, Kansu, Aydan

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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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Clinical Features and HSCT Outcome for SCID in Turkey von Ikinciogullari, Aydan, Cagdas, Deniz, Dogu, Figen, Tugrul, Tuba, Karasu, Gulsum, Haskologlu, Sule, Aksoylar, Serap, Uygun, Vedat, Kupesiz, Alphan, Yildiran, Alisan, Gursel, Orhan, Ates, Can, Elhan, Atilla, Kansoy, Savas, Yesilipek, Akif, Tezcan, Ilhan

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Pediatric Invasive Aspergillosis: a Retrospective Review of 59 Cases von Özen, Seval, Özdemir, Halil, Taşkin, Esra Çakmak, Arga, Gül, Konca, Hatice Kübra, Çakmakli, Hasan Fatih, Haskoloğlu, Şule, Okulu, Emel, Dinçaslan, Handan, İnce, Elif, İleri, Talia, Taçyildiz, Nurdan, Doğu, Figen, Evren, Ebru, Us, Ebru, Karahan, Zeynep Ceren, Fitöz, Suat, Kendirli, Tanıl, Kuloğlu, Zarife, Tutar, Ercan, İkincioğullari, Aydan, Ünal, Emel, Ertem, Mehmet, İnce, Erdal, Çiftçi, Ergin

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Clinical Features and Outcomes of 23 Patients with Wiskott-Aldrich Syndrome: A Single-Center Experience von Haskologlu, Sule, Ozturk, Aysenur, Ozturk, Gokcan, Bal, Sevgi Kostel, Islamoglu, Candan, Baskin, Kubra, Ceylaner, Serdar, Satiroglu, Lale Tufan, Dogu, Figen, Ikinciogullari, Aydan

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Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and Outcomes von Bayram, Ozlem, Haskologlu, Sule, Bayrakoğlu, Deniz, Bal, Sevgi Kostel, Islamoglu, Candan, Cipe, Funda Erol, Kendirli, Tanil, Kursun, Nazmiye, Guner, Sukru Nail, Yildiran, Alisan, Bozdogan, Gunseli, Yuksek, Mutlu, Reisli, Ismail, Dalva, Klara, Aytekin, Caner, Boztug, Kaan, Dogu, Figen, Ikinciogullari, Aydan

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Newborn screening for SCID: the very first prospective pilot study from Türkiye von Haskologlu, Sule, Kocak, Senem, Tufan, Lale Satiroglu, Aksoy, Fethiye Eken, Bastug, Dilan, Oner, Deniz Aslar, Islamoglu, Candan, Baskin, Kubra, Esenboga, Saliha, Acican, Deniz, Ceylaner, Serdar, Guner, Sukru Nail, Keles, Sevgi, Cagdas, Deniz, Reisli, Ismail, Tezel, Basak, Dogu, Figen, Tezcan, Ilhan, Ikinciogullari, Aydan

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Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations von Giardino, Giuliana, Sharapova, Svetlana O., Ciznar, Peter, Dhalla, Fatima, Maragliano, Luca, Radha Rama Devi, Akella, Islamoglu, Candan, Ikinciogullari, Aydan, Haskologlu, Sule, Dogu, Figen, Hanna-Wakim, Rima, Dbaibo, Ghassan, Chou, Janet, Cirillo, Emilia, Borzacchiello, Carla, Kreins, Alexandra Y., Worth, Austen, Rota, Ioanna A., Marques, José G., Sayitoglu, Muge, Firtina, Sinem, Mahdi, Moaffaq, Geha, Raif, Neven, Bénédicte, Sousa, Ana E., Benfenati, Fabio, Hollander, Georg A., Davies, E. Graham, Pignata, Claudio

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Scales of Magt1 Gene: Novel Mutations, Different Presentations von Haskologlu, Sule, Baskin, Kubra, Aytekin, Caner, Islamoglu, Candan, Ceylaner, Serdar, Dogu, Figen, Tacyildiz, Nurdan, Unal, Emel, Ikinciogullari, Aydan

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Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency? von Öztürk, Gökcan, Haskoloğlu, Şule, Deveci, Nazlı, Erkmen, Hasret, Çelik, Nur Ayça, Sucak, Gülsan, Ceylaner, Serdar, İkincioğulları, Aydan, Doğu, Figen

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