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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Evaluation of children with chronic cough including obstructive sleep apnea: a single-center experience von Ilarslan, Nisa Eda Cullas, Gunay, Fatih, Haskologlu, Zehra Sule, Bal, Sevgi Kostel, Tezcaner, Zahide Ciler, Kirsaclioglu, Ceyda Tuna, Firat, Selma, Altuntas, Cansu, Ciftci, Bulent, Ozgursoy, Ozan Bagis, Cobanoglu, Nazan

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Allogeneic hematopoietic stem cell and liver transplantation in a young girl with dedicator of cytokinesis 8 protein deficiency von Kuloglu, Zarife, Balcı, Deniz, Haskoloğlu, Zehra Şule, Kendirli, Tanıl, Bingöl‐Koloğlu, Meltem, Tuna‐Kırsaçlıoğlu, Ceyda, Bal, Sevgi, Selbuz, Suna, Kırımker, Onur, Savaş, Berna, Altuntaş, Cansu, Güner, Şükrü Nail, Can, Özlem Selvi, Karayalçın, Kaan, Doğu, Figen, Kansu Tanca, Aydan, İkincioğulları, Aydan

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Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention von Kotlarz, Daniel, Egritas Gurkan, Odul, Haskologlu, Zehra Sule, Ekinci, Ozgur, Aksu Unlusoy, Aysel, Gürcan Kaya, Neslihan, Puchalka, Jacek, Klein, Cristoph, Dalgic, Buket

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Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency von Taghizade, Nigar, Babayeva, Royala, Kara, Altan, Karakus, Ibrahim Serhat, Catak, Mehmet Cihangir, Bulutoglu, Alper, Haskologlu, Zehra Sule, Akay Haci, Idil, Tunakan Dalgic, Ceyda, Karabiber, Esra, Bilgic Eltan, Sevgi, Yorgun Altunbas, Melek, Sefer, Asena Pinar, Sezer, Ahmet, Kokcu Karadag, Sefika Ilknur, Arik, Elif, Karali, Zuhal, Ozhan Kont, Aylin, Tuzer, Can, Karaman, Sait, Mersin, Selver Seda, Kasap, Nurhan, Celik, Enes, Kocacik Uygun, Dilara Fatma, Aydemir, Sezin, Kiykim, Ayca, Aydogmus, Cigdem, Ozek Yucel, Esra, Celmeli, Fatih, Karatay, Emrah, Bozkurtlar, Emine, Demir, Semra, Metin, Ayse, Karaca, Neslihan Edeer, Kutukculer, Necil, Aksu, Guzide, Guner, Sukru Nail, Keles, Sevgi, Reisli, Ismail, Kendir Demirkol, Yasemin, Arikoglu, Tugba, Gulez, Nesrin, Genel, Ferah, Kilic, Sara Sebnem, Aytekin, Caner, Keskin, Ozlem, Yildiran, Alisan, Ozcan, Dilek, Altintas, Derya Ufuk, Ardeniz, Fatma Omur, Dogu, Esin Figen, Ikinciogullari, Kamile Aydan, Karakoc-Aydiner, Elif, Ozen, Ahmet, Baris, Safa

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DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans von Azizoglu, Zehra Busra, Babayeva, Royala, Haskologlu, Zehra Sule, Acar, Mustafa Burak, Ayaz-Guner, Serife, Okus, Fatma Zehra, Alsavaf, Mohammad Bilal, Can, Salim, Basaran, Kemal Erdem, Canatan, Mehmed Fatih, Ozcan, Alper, Erkmen, Hasret, Leblebici, Can Berk, Yilmaz, Ebru, Karakukcu, Musa, Kose, Mehmet, Canoz, Ozlem, Özen, Ahmet, Karakoc-Aydiner, Elif, Ceylaner, Serdar, Gümüş, Gülsüm, Per, Huseyin, Gumus, Hakan, Canatan, Halit, Ozcan, Servet, Dogu, Figen, Ikinciogullari, Aydan, Unal, Ekrem, Baris, Safa, Eken, Ahmet

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Correction to: DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans von Azizoglu, Zehra Busra, Babayeva, Royala, Haskologlu, Zehra Sule, Acar, Mustafa Burak, Ayaz-Guner, Serife, Okus, Fatma Zehra, Alsavaf, Mohammad Bilal, Can, Salim, Basaran, Kemal Erdem, Canatan, Mehmed Fatih, Ozcan, Alper, Erkmen, Hasret, Leblebici, Can Berk, Yilmaz, Ebru, Karakukcu, Musa, Kose, Mehmet, Canoz, Ozlem, Özen, Ahmet, Karakoc-Aydiner, Elif, Ceylaner, Serdar, Gümüş, Gülsüm, Per, Huseyin, Gumus, Hakan, Canatan, Halit, Ozcan, Servet, Dogu, Figen, Ikinciogullari, Aydan, Unal, Ekrem, Baris, Safa, Eken, Ahmet

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Mycobacterium bovis Bacillus Calmette-Guérin (BCG)-Related Sternal Osteomyelitis von Inceli, Belkis Hatice, Penezoglu, Döndü Nilay, Özdemir, Halil, Arga, Gül, Kaynak Sahap, Seda, Fitoz, Ömer Suat, Ceyhan, Koray, Kayi Cangir, Ayten, Haskologlu, Zehra Sule, Çiftçi, Ergin

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Endocrinopathy In Primary Immunodeficiency Patients: A Single Center Retrospective Study von BAYRAK DURMAZ, Makbule Seda, UNUTMAZ, Done Gulcin, ERKOC, Merve, HASKOLOGLU, Zehra Sule, DOGU, Esin Figen, IKINCIOGULLARI, Kamile Aydan, KESKIN, Goksal, ALTINER, Seda

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Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases von Dönger, Utku, Warasnhe, Khaled, Özçay, Figen, Şule Haskoloğlu, Zehra, İbrahim Aydın, Halil, Ceylaner, Serdar

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Does the Hyper IgM Phenotype Affect Prognosis in Ataxia Telangiectasia? von HASKOLOĞLU, Zehra Şule, Aytekin, Caner, Köstel Bal, Sevgi, İslamoğlu, Candan, Baskın, Kübra, Yavuz, Zeynep, Altun, Demet, Ceylaner, Serdar, Doğu, Figen, İkincioğulları, Aydan

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Immunoglobulin Isotype Deficiency Together with Allergic Diseases von Altun, Demet, Akpınar, Melis, Haskoloğlu, Zehra Şule, Köste Bal, Sevgi, Kavgacı, Akif, Doğu, Esin Figen, İkincioğulları, Kamile Aydan

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T Regulatory Cells in Children with Atopic Dermatitis von Çiftçi, Ömer, Haskoloğlu, Zehra Şule, Güloğlu, Deniz, Çipe, Funda, Çiftçi, Aylin, Köse, Kenan, Doğu, Figen, İkincioğulları, Aydan

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Is There a Relationship between Clinical Symptoms of Asthmatic Children and Serum Levels of Vitamin D and Zinc? von Haskoloğlu, Zehra Şule, Altun, Demet

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Serum Chitotriosidase Activity in Bronchopulmonary Dysplasia: A Cross-Sectional Study von Eminoğlu, Fatma Tuba, Keleştemur, Elif, Doğan, Özlem, Köse, Engin, Haskoloğlu, Zehra Şule, Çobanoğlu, Nazan

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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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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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Astımlı Çocukların Serum D Vitamini ve Çinko Düzeyleri ile Klinik Bulguları Arasında Bir İlişki Var mı? von Zehra Şule Haskoloğlu, Demet Altun

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Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention von Kotlarz, Daniel, Egritas Gurkan, Odul, Haskologlu, Zehra Sule, Ekinci, Ozgur, Aksu Unlusoy, Aysel, Gürcan Kaya, Neslihan, Puchalka, Jacek, Klein, Cristoph, Dalgic, Buket

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Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases von Dönger, Utku, Warasnhe, Khaled, Özçay, Figen, Şule Haskoloğlu, Zehra, İbrahim Aydın, Halil, Ceylaner, Serdar

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