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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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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Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis von Taşkıran, Ekim Z., Sönmez, Hafize E., Ayvaz, Deniz Ç., Koşukcu, Can, Batu, Ezgi D., Esenboğa, Saliha, Topaloğlu, Rezan, Orhan, Diclehan, Bilginer, Yelda, Alikaşifoğlu, Mehmet, Özen, Seza, Tezcan, İlhan

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Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association von Yee, Christina S., MD, PhD, Massaad, Michel J., PhD, Bainter, Wayne, BA, Ohsumi, Toshiro K., PhD, Föger, Niko, PhD, Chan, Andrew C., MD, PhD, Akarsu, Nurten A., MD, Aytekin, Caner, MD, Ayvaz, Deniz Çagdas, MD, PhD, Tezcan, Ilhan, MD, PhD, Sanal, Özden, MD, Geha, Raif S., MD, Chou, Janet, MD

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Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in... von Erman, Baran, Aba, Umran, Ipsir, Canberk, Pehlivan, Damla, Aytekin, Caner, Cildir, Gökhan, Cicek, Begum, Bozkurt, Ceren, Tekeoglu, Sidem, Kaya, Melisa, Aydogmus, Cigdem, Cipe, Funda, Sucak, Gulsan, Eltan, Sevgi Bilgic, Ozen, Ahmet, Barıs, Safa, Karakoc-Aydiner, Elif, Kıykım, Ayca, Karaatmaca, Betul, Kose, Hulya, Uygun, Dilara Fatma Kocacık, Celmeli, Fatih, Arikoglu, Tugba, Ozcan, Dilek, Keskin, Ozlem, Arık, Elif, Aytekin, Elif Soyak, Cesur, Mahmut, Kucukosmanoglu, Ercan, Kılıc, Mehmet, Yuksek, Mutlu, Bıcakcı, Zafer, Esenboga, Saliha, Ayvaz, Deniz Çagdaş, Sefer, Asena Pınar, Guner, Sukrü Nail, Keles, Sevgi, Reisli, Ismail, Musabak, Ugur, Demirbas, Nazlı Deveci, Haskologlu, Sule, Kilic, Sara Sebnem, Metin, Ayse, Dogu, Figen, Ikinciogulları, Aydan, Tezcan, Ilhan

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In case of recurrent wheezing and bronchiolitis: Think again, it may be a primary immunodeficiency von Ozbek, Begum, Ayvaz, Deniz Çağdaş, Esenboga, Saliha, Halaçlι, Sevil Oskay, Aytekin, Elif Soyak, Yaz, Ismail, Tan, Çağman, Tezcan, Ilhan

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Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M syndrome and with LGLL von Bajin, İnci Yaman, Ayvaz, Deniz Çağdaş, Ünal, Şule, Özgür, Tuba Turul, Çetin, Mualla, Gümrük, Fatma, Tezcan, İlhan, de Villartay, Jean-Pierre, Sanal, Özden

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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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Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS von Tan, Çağman, Özgül, Rıza Köksal, Çağdaş Ayvaz, Deniz, Tezcan, İlhan, Sanal, Özden

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DiGeorge Syndrome: Simultaneously Diagnosis of A Mother-Baby Pair With Great Clinical Variability von Sırma Dokuzboy,Refika, Sarı,Fatma Nur, Beşer Özmen,Esra, Ayvaz,Deniz Çağdaş, Alyamaç Dizdar,Evrim

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Successful treatment of severe myasthenia gravis developed after allogeneic hematopoietic stem cell transplantation with plasma exchange and rituximab von Unal, Sule, Sag, Erdal, Kuskonmaz, Baris, Kesici, Selman, Bayrakci, Benan, Ayvaz, Deniz C., Tezcan, Ilhan, Yalnızoglu, Dilek, Uckan, Duygu

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CVID Associated with Systemic Amyloidosis von Sanal, Ozden, Peynircioglu, Banu, Saglam Ayhan, Arzu, Çagdas Ayvaz, Deniz, Esenboga, Saliha, Tezcan, Ilhan

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Defective pneumococcal antibody response in patients with recurrent respiratory tract infections von Erman, Baran, Demirtaş, Duygu, Bildik, Hacer Neslihan, Çağdaş-Ayvaz, Deniz, Sanal, Özden, Tezcan, İlhan

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Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss von Gür-Çetinkaya, Pınar, Çağdaş-Ayvaz, Deniz Nazire, Öksüz, Ayça Burcu, Ertoy, Ayşe, Hayran, Umut, Özkan, Feride, Erol, Meliha, Tezcan, İlhan

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Additional Diverse Findings Expand the Clinical Presentation of DOCK8 Deficiency von Sanal, Ozden, Jing, Huie, Ozgur, Tuba, Ayvaz, Deniz, Strauss-Albee, Dara M., Ersoy-Evans, Sibel, Tezcan, Ilhan, Turkkani, Gulten, Matthews, Helen F., Haliloglu, Goknur, Yuce, Aysel, Yalcin, Bilgehan, Gokoz, Ozay, Oguz, Kader K., Su, Helen C.

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Coronin-1A Oligomerization Is Critical For Host Defense Against Viral Pathogens von Yee, Christina S.K., MD, PhD, Sanal, Ozden, MD, Chou, Janet S., MD, Geha, Raif S., MD, Ayvaz, Deniz, MD, Aytekin, Caner, MD, Akarsu, A. Nurten, MD, PhD

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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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Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype von Toubiana, Julie, Okada, Satoshi, Hiller, Julia, Oleastro, Matias, Lagos Gomez, Macarena, Aldave Becerra, Juan Carlos, Ouachée-Chardin, Marie, Fouyssac, Fanny, Girisha, Katta Mohan, Etzioni, Amos, Van Montfrans, Joris, Camcioglu, Yildiz, Kerns, Leigh Ann, Belohradsky, Bernd, Blanche, Stéphane, Bousfiha, Aziz, Rodriguez-Gallego, Carlos, Meyts, Isabelle, Kisand, Kai, Reichenbach, Janine, Renner, Ellen D., Rosenzweig, Sergio, Grimbacher, Bodo, van de Veerdonk, Frank L., Traidl-Hoffmann, Claudia, Picard, Capucine, Marodi, Laszlo, Morio, Tomohiro, Kobayashi, Masao, Lilic, Desa, Milner, Joshua D., Holland, Steven, Casanova, Jean-Laurent, Puel, Anne

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First allogeneic hematopoietic stem cell transplantation in RASGRP1 deficiency: long-term follow-up von Kuskonmaz, Baris, Ayvaz, Deniz, Okur, Fatma Visal, Aydın, Burça, Tezcan, Ilhan, Uckan Cetinkaya, Duygu

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STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation von Halacli, Sevil Oskay, Ayvaz, Deniz Cagdas, Sun-Tan, Cagman, Erman, Baran, Uz, Elif, Yilmaz, Didem Yucel, Ozgul, Koksal, Tezcan, İlhan, Sanal, Ozden

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