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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Patients with Primary Immunodeficiencies in Pediatric Intensive Care Unit: Outcomes and Mortality-Related Risk Factors von Ödek, Çağlar, Kendirli, Tanıl, Doğu, Figen, Yaman, Ayhan, Vatansever, Göksel, Çipe, Funda, Haskoloğlu, Şule, Ateş, Can, İnce, Erdal, İkincioğulları, Aydan

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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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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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Clinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience von Haskoloğlu, Şule, Öztürk, Ayşenur, Öztürk, Gökcan, Kostel Bal, Sevgi, İslamoğlu, Candan, Baskın, Kübra, Ceylaner, Serdar, Tufan Satıroğlu, Lale, Doğu, Figen, İkincioğulları, 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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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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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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ST2 and Reg3α: Can they predict aGvHD, steroid refractoriness and transplant-related mortality in pediatric patients after HSCT? von Öztürk, Gökcan, Bayrakoğlu, Deniz, Haskoloğlu, Şule, Baskın, Kübra, Deveci, Nazlı, İnce, Elif, İleri, Talia, Çakmaklı, Hasan, Ertem, Mehmet, İkincioğulları, Aydan, Doğu, Figen

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A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection von Kaya, Zühre, Muluk, Cansu, Hakoloğlu, Şule, Tufan, Lale Ş.

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Pediatric Invasive Aspergillosis: A Retrospective Review of 59 Cases von ÖZEN, Seval, ÖZDEMİR, Halil, TAŞKIN, Esra ÇAKMAK, ARGA, Gül, KONCA, Hatice Kübra, ÇAKMAKLI, Hasan Fatih, HASKOLOĞLU, Şule, OKULU, Emel, DİNÇASLAN, Handan, İNCE, Elif, İLERİ, Talia, TAÇYILDIZ, Nurdan, DOĞU, Figen, EVREN, Ebru, US, Ebru, KARAHAN, Zeynep Ceren, FİTÖZ, Suat, KENDİRLİ, Tanıl, KULOĞLU, Zarife, TUTAR, Ercan, İKİNCİOĞULLARI, Aydan, ÜNAL, Emel, ERTEM, Mehmet, İNCE, Erdal, ÇİFTÇİ, Ergin

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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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Evaluation of thymopoiesis in healthy Turkish children aged 0-6 years von Kavgacı, Akif, Doğu, Figen, Arıkan, Meltem, İslamoğlu, Candan, Okulu, Emel, Topçu, Seda, Çullas-İlarslan, Nisa Eda, Haskoloğlu, Şule, Bal, Sevgi Köstel, Bayrakoğlu, Deniz, İkincioğulları, Kamile Aydan

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Outcome of treosulfan‐based reduced‐toxicity conditioning regimens for HSCT in high‐risk patients with primary immune deficiencies von Haskoloğlu, Şule, Köstel Bal, Sevgi, İslamoğlu, Candan, Altun, Demet, Kendirli, Tanıl, Doğu, Esin Figen, İkincioğulları, Aydan

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Eosinophilia and Increased Immunoglobulin E: Is It Really a Primary Immunodeficiency? A Diagnostic Challenge von Öztürk, Gökcan, Parlar, Tutku, Haskoloğlu, Şule, Baskın, Kübra, Deveci, Nazlı, Çiftçi, Ergin, Doğu, Figen, İkincioğulları, Aydan

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Primary antibody deficiencies in Turkey: molecular and clinical aspects von Firtina, Sinem, Ng, Yuk Yin, Ng, Ozden H., Kiykim, Ayca, Ozek, Esra Yucel, Kara, Manolya, Aydiner, Elif, Nepesov, Serdar, Camcioglu, Yildiz, Sayar, Esra H., Gungoren, Ezgi Yalcin, Reisli, Ismail, Torun, Selda H., Haskologlu, Sule, Cogurlu, Tuba, Kaya, Aysenur, Cekic, Sukru, Baris, Safa, Ozbek, Ugur, Ozen, Ahmet, Sayitoglu, Muge

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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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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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