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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Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia von Acar, Buket, Cagdas, Deniz, Tan, Çağman, Özbek, Begüm, Yaz, İsmail, Yıldırım, Yağmur Deniz, Özşin-Özler, Cansu, Karaatmaca, Betül, Gür-Çetinkaya, Pınar, Soyak, Elif, Karabulut, Erdem, Tezcan, İlhan, Berker, Ezel

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Effects of oral prophylaxis including tongue cleaning on halitosis and gingival inflammation in gingivitis patients—a randomized controlled clinical trial von Acar, Buket, Berker, Ezel, Tan, Çağman, İlarslan, Yağmur D., Tekçiçek, Meryem, Tezcan, İlhan

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A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc von Cagdas, Deniz, Yılmaz, Mustafa, Kandemir, Nurgün, Tezcan, İlhan, Etzioni, Amos, Sanal, Özden

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Nutritional status of children with primary immunodeficiency: A single center experience von Karhan, Asuman Nur, Esenboğa, Saliha, Gümüş, Ersin, Karaatmaca, Betül, Cagdas, Deniz, Demir, Hülya, Saltik Temizel, İnci Nur, Özen, Hasan, Yüce, Aysel, Tezcan, İlhan

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Correction to: Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia von Acar, Buket, Cagdas, Deniz, Tan, Çağman, Özbek, Begüm, Yaz, İsmail, Yıldırım, Yağmur Deniz, Özşin-Özler, Cansu, Karaatmaca, Betül, Gür-Çetinkaya, Pınar, Soyak, Elif, Karabulut, Erdem, Tezcan, İlhan, Berker, Ezel

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Evaluation of the peripheral blood T and B cell subsets and IRF‐7 variants in adult patients with severe influenza virus infection von Çalık Başaran, Nursel, Tan, Çağman, Özışık, Lale, Özbek, Begüm, İnkaya, Ahmet Çağkan, Alp, Şehnaz, Ersoy, Ebru Ortaç, Ayvaz, Deniz Çağdaş, Tezcan, İlhan

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Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients von Tan, Çağman, Çağdaş-Ayvaz, Deniz, Metin, Ayşe, Keskin, Özlem, Tezcan, İlhan, Sanal, Özden

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COVID-19 in Patients with Primary Immunodeficiency von Esenboga, Saliha, Ocak, Melike, Akarsu, Ayşegul, Bildik, Hacer Neslihan, Cagdas, Deniz, Iskit, Arzu Topeli, Tezcan, Ilhan

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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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Detection of parasites in children with chronic diarrhea von Maçin, Salih, Kaya, Filiz, Çağdaş, Deniz, Hizarcioglu-Gulsen, Hayriye, Saltik-Temizel, Inci Nur, Tezcan, İlhan, Demir, Hülya, Ergüven, Sibel, Akyön, Yakut

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Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency von Cicalese, Maria Pia, Ferrua, Francesca, Castagnaro, Laura, Pajno, Roberta, Barzaghi, Federica, Giannelli, Stefania, Dionisio, Francesca, Brigida, Immacolata, Bonopane, Marco, Casiraghi, Miriam, Tabucchi, Antonella, Carlucci, Filippo, Grunebaum, Eyal, Adeli, Mehdi, Bredius, Robbert G., Puck, Jennifer M., Stepensky, Polina, Tezcan, Ilhan, Rolfe, Katie, De Boever, Erika, Reinhardt, Rickey R., Appleby, Jonathan, Ciceri, Fabio, Roncarolo, Maria Grazia, Aiuti, Alessandro

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Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R von Erman, Baran, Bilic, Ivan, Hirschmugl, Tatjana, Salzer, Elisabeth, Çagdas, Deniz, Esenboga, Saliha, Akcoren, Zuhal, Sanal, Ozden, Tezcan, Ilhan, Boztug, Kaan

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Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function von Shahin, Tala, Aschenbrenner, Dominik, Cagdas, Deniz, Bal, Sevgi Köstel, Conde, Cecilia Domínguez, Garncarz, Wojciech, Medgyesi, David, Schwerd, Tobias, Karaatmaca, Betül, Cetinkaya, Pınar Gur, Esenboga, Saliha, Twigg, Stephen R F, Cant, Andrew, Wilkie, Andrew O M, Tezcan, Ilhan, Uhlig, Holm H, Boztug, Kaan

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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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A clinical score to guide in decision making for monogenic type I IFNopathies von Sönmez, Hafize Emine, Karaaslan, Cagatay, de Jesus, Adriana A., Batu, Ezgi Deniz, Anlar, Banu, Sözeri, Betül, Bilginer, Yelda, Karaguzel, Dilara, Cagdas Ayvaz, Deniz, Tezcan, Ilhan, Goldbach-Mansky, Raphaela, Ozen, Seza

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Hematologically important mutations: Leukocyte adhesion deficiency (first update) von van de Vijver, Edith, Maddalena, Anne, Sanal, Özden, Holland, Steven M., Uzel, Gulbu, Madkaikar, Manisha, de Boer, Martin, van Leeuwen, Karin, Köker, M. Yavuz, Parvaneh, Nima, Fischer, Alain, Law, S.K. Alex, Klein, Nigel, Tezcan, F. Ilhan, Unal, Ekrem, Patiroglu, Turkan, Belohradsky, Bernd H., Schwartz, Klaus, Somech, Raz, Kuijpers, Taco W., Roos, Dirk

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Selective IgM deficiency: Follow‐up and outcome von Caka, Canan, Cimen, Ozlem, Kahyaoğlu, Pinar, Tezcan, İlhan, Cagdas, Deniz, Atanaskovic‐Markovic, Marina

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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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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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