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Membership type: full

Deniz N. Cagdas Ayvaz

Country of origin: Republic of Türkiye Currently in: Republic of Türkiye, Ankara General field of specialization: Medical and Health Sciences incl Neurosciences
Academic Background

Degrees

1998 Undergraduate Medical and Health Sciences incl Neurosciences
2004 Master Medical and Health Sciences incl Neurosciences
2017 Doctorate Medical and Health Sciences incl Neurosciences
Research and Profession

Current Research Activities

Medical and Health Sciences incl Neurosciences

After graduating from Hacettepe University Faculty of Medicine, Dr. Cagdas Ayvaz have taken specialty education at the Department of Pediatrics of Hacettepe University Faculty of Medicine between 1999 and 2004. She studied for four years on congenital and acquired heart diseases of childhood at Pediatric Cardiology Clinic of Ankara Yuksek Ihtisas Education and Training Hospital and she did researches on heart diseases of childhood, childhood obesity and treatment. She started the subspecialty education at the Department of Pediatrics of Hacettepe University of Faculty of Medicine in 2009. She started the doctorate program on Immunology in 2012. She became academic member and assistant professor doctor in 2012, and became associate professor of Pediatrics at the same department in 2012. Her professional interests include primary immunodeficiencies and their molecular basis, hematopoietic stem cell transplantation in primary immunodeficiencies, the systemic and immunologic effects of infections on immune system, disorders of immunodysregulation and lymphoproliferation.


Publications resulting from Research: 


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Süleyman M, Serin O, Koçali B, Orhan D, Yalçın EE, Özçelik U, Ceyhan M, Kiper N, Tezcan İ, Dogru D, Çağdaş D. High Inborn Errors of Immunity Risk in Patients with Granuloma. J Clin Immunol. 2022 Aug 18;. doi: 10.1007/s10875-022-01342-1. [Epub ahead of print] PubMed PMID: 35980494.

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Sener S, Basaran O, Batu ED, Atalay E, Esenboga S, Cagdas D, Kuskonmaz BB, Bilginer Y, Ozaltin F, Oguz B, Duzova A, Tezcan I, Ozen S. Childhood-onset Takayasu arteritis and immunodeficiency: case-based review. Clin Rheumatol. 2022 Jul 20;. doi: 10.1007/s10067-022-06295-9. [Epub ahead of print] Review. PubMed PMID: 35854168.

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Ayan G, Yagiz B, Cinar OE, Cagdas D, Ozbek DA, Tuncer A, Oguz KK, Ozen S, Alikasifoglu M, Karadag O. A novel variant in severe disease of DADA2: involving vasculitic and haematologic features. Scand J Rheumatol. 2022 Jul 19;:1-3. doi: 10.1080/03009742.2022.2095724. [Epub ahead of print] PubMed PMID: 35852217.

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Bildik HN, Cagdas D, Ozturk Kura A, Oskay Halacli S, Sanal O, Tezcan I. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study. Immunol Invest. 2022 Jul;51(5):1272-1283. doi: 10.1080/08820139.2021.1933516. Epub 2021 Jun 7. PubMed PMID: 34098853.

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Acar B, Gümüş E, Özcan-Bulut S, Özşin-Özler C, Boyraz MS, Tan Ç, Yaz I, Özbek B, Cagdas D, Saltık-Temizel İN, Demir H, Özen H, Karabulut E, Tezcan İ, Yüce A, Berker E. Cytokine profile in serum and gingival crevicular fluid of children with inflammatory bowel disease: A case-control study. J Periodontol. 2022 Jul;93(7):1048-1059. doi: 10.1002/JPER.21-0514. Epub 2021 Dec 22. PubMed PMID: 34730850.

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Kuskonmaz B, Ayvaz D, Okur FV, Aydın B, Tezcan I, Uckan Cetinkaya D. First allogeneic hematopoietic stem cell transplantation in RASGRP1 deficiency: long-term follow-up. Bone Marrow Transplant. 2022 Jul;57(7):1210-1212. doi: 10.1038/s41409-022-01704-8. Epub 2022 May 14. PubMed PMID: 35568755; PubMed Central PMCID: PMC9106979.

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Ozsezen B, Yalçın E, Ademhan Tural D, Sunman B, Nayır Buyuksahin H, Guzelkas İ, Alboga D, Aytekin ES, Esenboga S, Emiralioglu N, Cagdas D, Doğru D, Özçelik U, Tezcan I, Kiper N. Antimycobacterial prophylaxis regarding Bacillus Calmette-Guérin -associated complications in children with primary immunodeficiency. Respir Med. 2022 Jun 16;200:106919. doi: 10.1016/j.rmed.2022.106919. [Epub ahead of print] PubMed PMID: 35779416.

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Yao Y, Du Jiang P, Chao BN, Cagdas D, Kubo S, Balasubramaniyam A, Zhang Y, Shadur B, NaserEddin A, Folio LR, Schwarz B, Bohrnsen E, Zheng L, Lynberg M, Gottlieb S, Leney-Greene MA, Park AY, Tezcan I, Akdogan A, Gocmen R, Onder S, Rosenberg A, Soilleux EJ, Johnson E, Jackson PK, Demeter J, Chauvin SD, Paul F, Selbach M, Bulut H, Clatworthy MR, Tuong ZK, Zhang H, Stewart BJ, Bosio CM, Stepensky P, Clare S, Ganesan S, Pascall JC, Daumke O, Butcher GW, McMichael AJ, Simon AK, Lenardo MJ. GIMAP6 regulates autophagy, immune competence, and inflammation in mice and humans. J Exp Med. 2022 Jun 6;219(6). doi: 10.1084/jem.20201405. Epub 2022 May 13. PubMed PMID: 35551368; PubMed Central PMCID: PMC9111091.

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Demirtas D, Cagdas D, Turul Ozgur T, Kuskonmaz B, Uckan Cetinkaya D, Sanal O, Tezcan I. Long Term Follow-Up of the Patients with Severe Combined Immunodeficiency After Hematopoietic Stem Cell Transplantation: A Single-Center Study. Immunol Invest. 2022 May;51(4):739-747. doi: 10.1080/08820139.2020.1869776. Epub 2021 Jan 21. PubMed PMID: 33472463.

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Esenboga S, Cagdas D, Alkanat NE, Güler Tezel G, Ersoy Evans S, Boztug K, Tezcan I. TMC8 mutation in a Turkish family with epidermodysplasia verruciformis including laryngeal papilloma and recurrent skin carcinoma. J Cosmet Dermatol. 2022 May;21(5):2263-2267. doi: 10.1111/jocd.14393. Epub 2021 Aug 20. PubMed PMID: 34416085.

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Süleyman M, Tan Ç, Uner A, İnkaya Ç, Aytaç S, Büyükaşık Y, Boztug K, Tezcan İ, Cagdas D. Adenosine Deaminase Type II Deficiency: Severe Chronic Neutropenia, Lymphoid Infiltration in Bone Marrow, and Inflammatory Features. Immunol Invest. 2022 Apr;51(3):558-566. doi: 10.1080/08820139.2020.1853153. Epub 2020 Dec 2. PubMed PMID: 33705245.

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Torun B, Bilgin A, Orhan D, Gocmen R, Kılıc SS, Kuskonmaz B, Cetinkaya D, Tezcan I, Cagdas D. Combined immunodeficiency due to purine nucleoside phosphorylase deficiency: Outcome of three patients. Eur J Med Genet. 2022 Mar;65(3):104428. doi: 10.1016/j.ejmg.2022.104428. Epub 2022 Jan 19. PubMed PMID: 35063692.

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Saglam A, Cagdas D, Aydin B, Keles S, Reisli I, Arslankoz S, Katipoglu K, Uner A. STK4 deficiency and EBV-associated lymphoproliferative disorders, emphasis on histomorphology, and review of literature. Virchows Arch. 2022 Feb;480(2):393-401. doi: 10.1007/s00428-021-03147-w. Epub 2021 Oct 4. Review. PubMed PMID: 34604912.

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Çalık Başaran N, Tan Ç, Özışık L, Özbek B, İnkaya AÇ, Alp Ş, Ersoy EO, Ayvaz DÇ, Tezcan İ. Evaluation of the peripheral blood T and B cell subsets and IRF-7 variants in adult patients with severe influenza virus infection. Health Sci Rep. 2022 Jan;5(1):e492. doi: 10.1002/hsr2.492. eCollection 2022 Jan. PubMed PMID: 35229048; PubMed Central PMCID: PMC8865064.

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Karhan AN, Esenboğa S, Gümüş E, Karaatmaca B, Cagdas D, Demir H, Saltik Temizel İN, Özen H, Yüce A, Tezcan İ. Nutritional status of children with primary immunodeficiency: A single center experience. Pediatr Int. 2022 Jan;64(1):e14996. doi: 10.1111/ped.14996. Epub 2021 Nov 23. PubMed PMID: 34533857.

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Aydin Goker ET, Cagdas D, Bajin IY, Kukul MG, Aytekin ES, Orhan D, Alp A, Uzar S, Sarac F, Kara A, Kutluk MT. Multicentric Castleman disease in a DOCK8-deficient patient with Orf virus infection. Pediatr Allergy Immunol. 2022 Jan;33(1):e13666. doi: 10.1111/pai.13666. Epub 2021 Nov 18. PubMed PMID: 34792227.

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Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, de Boer M, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Garcia-Morato MB, Shephard JLV, Cagdas D, Tezcan I, Sherkat R, Mortaz E, Fayezi A, Shahrooei M, Wolach B, Blancas-Galicia L, Kanegane H, Kawai T, Condino-Neto A, Vihinen M, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update). Blood Cells Mol Dis. 2021 Dec;92:102596. doi: 10.1016/j.bcmd.2021.102596. Epub 2021 Jul 28. PubMed PMID: 34547651.

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Esenboga S, Oguz B, Cagdas D, Karaatmaca B, Emiralioglu N, Yalcin E, Dogru D, Ozcelik U, Kiper N, Tezcan İ. Respiratory system findings in pediatric patients with primary immunodeficiency. Pediatr Pulmonol. 2021 Dec;56(12):4011-4019. doi: 10.1002/ppul.25657. Epub 2021 Sep 9. PubMed PMID: 34499824.

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Gülseren D, Tan Ç, Yaz İ, Özbek B, Çağdaş D, Tezcan İ. Expression of HLA class I and class II genes in patients with multiple skin warts. Exp Dermatol. 2021 Nov;30(11):1642-1649. doi: 10.1111/exd.14362. Epub 2021 May 5. PubMed PMID: 33896076.

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Cagdas D. Maternofetal Transfusion, Maternal Chimerism, and Maternal Engraftment: A Mystery in Health and Disease. J Allergy Clin Immunol Pract. 2021 Nov;9(11):4154-4155. doi: 10.1016/j.jaip.2021.08.022. PubMed PMID: 34749950.

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Yaz I, Ozbek B, Bildik HN, Tan C, Oskay Halacli S, Soyak Aytekin E, Esenboga S, Cekic S, Kilic SS, Keskin O, van Leeuwen K, Roos D, Cagdas D, Tezcan I. Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey. Clin Exp Immunol. 2021 Oct;206(1):47-55. doi: 10.1111/cei.13645. Epub 2021 Aug 5. PubMed PMID: 34310689; PubMed Central PMCID: PMC8446394.

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Esenboga S, Ocak M, Akarsu A, Bildik HN, Cagdas D, Iskit AT, Tezcan I. COVID-19 in Patients with Primary Immunodeficiency. J Clin Immunol. 2021 Oct;41(7):1515-1522. doi: 10.1007/s10875-021-01065-9. Epub 2021 Jul 6. PubMed PMID: 34231093; PubMed Central PMCID: PMC8260154.

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Cagdas D, Halacli SO, Tan C, Esenboga S, Karaatmaca B, Cetinkaya PG, Balcı-Hayta B, Ayhan A, Uner A, Orhan D, Boztug K, Ozen S, Topaloglu R, Sanal O, Tezcan I. Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature. J Allergy Clin Immunol Pract. 2021 Oct;9(10):3752-3766.e4. doi: 10.1016/j.jaip.2021.05.032. Epub 2021 Jun 17. Review. PubMed PMID: 34146746.

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Soyak Aytekin E, Keskin A, Tan C, Yalçın E, Dogru D, Ozcelik U, Kiper N, Tezcan I, Cagdas D. Differential diagnosis of primary immunodeficiency in patients with BCGitis and BCGosis: A single-centre study. Scand J Immunol. 2021 Oct;94(4):e13084. doi: 10.1111/sji.13084. Epub 2021 Jul 28. PubMed PMID: 34780073.

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Ogishi M, Yang R, Aytekin C, Langlais D, Bourgey M, Khan T, Ali FA, Rahman M, Delmonte OM, Chrabieh M, Zhang P, Gruber C, Pelham SJ, Spaan AN, Rosain J, Lei WT, Drutman S, Hellmann MD, Callahan MK, Adamow M, Wong P, Wolchok JD, Rao G, Ma CS, Nakajima Y, Yaguchi T, Chamoto K, Williams SC, Emile JF, Rozenberg F, Glickman MS, Rapaport F, Kerner G, Allington G, Tezcan I, Cagdas D, Hosnut FO, Dogu F, Ikinciogullari A, Rao VK, Kainulainen L, Béziat V, Bustamante J, Vilarinho S, Lifton RP, Boisson B, Abel L, Bogunovic D, Marr N, Notarangelo LD, Tangye SG, Honjo T, Gros P, Boisson-Dupuis S, Casanova JL. Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child. Nat Med. 2021 Sep;27(9):1646-1654. doi: 10.1038/s41591-021-01388-5. Epub 2021 Jun 28. PubMed PMID: 34183838; PubMed Central PMCID: PMC8446316.

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Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Stasia MJ, Bakri FG, Köker N, Köker MY, Madkaika M, de Boer M, Garcia-Morato MB, Shephard JLV, Roesler J, Kanegane H, Kawai T, Di Matteo G, Shahrooei M, Bustamante J, Rawat A, Vignesh P, Mortaz E, Fayezi A, Cagdas D, Tezcan I, Kitcharoensakkul M, Dinauer MC, Meyts I, Wolach B, Condino-Neto A, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update). Blood Cells Mol Dis. 2021 Sep;90:102587. doi: 10.1016/j.bcmd.2021.102587. Epub 2021 Jun 2. Review. PubMed PMID: 34175765.

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Caka C, Cimen O, Kahyaoğlu P, Tezcan İ, Cagdas D. Selective IgM deficiency: Follow-up and outcome. Pediatr Allergy Immunol. 2021 Aug;32(6):1327-1334. doi: 10.1111/pai.13497. Epub 2021 Mar 29. PubMed PMID: 33706406.

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Cagdas D, Mayr D, Baris S, Worley L, Langley DB, Metin A, Aytekin ES, Atan R, Kasap N, Bal SK, Dmytrus J, Heredia RJ, Karasu G, Torun SH, Toyran M, Karakoc-Aydiner E, Christ D, Kuskonmaz B, Uçkan-Çetinkaya D, Uner A, Oberndorfer F, Schiefer AI, Uzel G, Deenick EK, Keller B, Warnatz K, Neven B, Durandy A, Sanal O, Ma CS, Özen A, Stepensky P, Tezcan I, Boztug K, Tangye SG. Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency. J Clin Immunol. 2021 Aug;41(6):1272-1290. doi: 10.1007/s10875-021-01031-5. Epub 2021 Apr 30. PubMed PMID: 33929673; PubMed Central PMCID: PMC8086229.

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Akar HT, Esenboga S, Cagdas D, Halacli SO, Ozbek B, van Leeuwen K, de Boer M, Tan CS, Köker Y, Roos D, Tezcan I. Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience. J Clin Immunol. 2021 Jul;41(5):992-1003. doi: 10.1007/s10875-021-01002-w. Epub 2021 Feb 24. PubMed PMID: 33629196.

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Ozbek B, Tan C, Yaz I, Kosukcu C, Esenboga S, Cetinkaya PG, Cagdas D, Tezcan I. Frequency of HLA Class I and Class II Alleles in Patients with CVID from Turkey. Immunol Invest. 2021 May;50(4):363-371. doi: 10.1080/08820139.2020.1759622. Epub 2020 May 5. PubMed PMID: 32370566.

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Acar B, Cagdas D, Tan Ç, Özbek B, Yaz İ, Yıldırım YD, Özşin-Özler C, Karaatmaca B, Gür-Çetinkaya P, Soyak E, Karabulut E, Tezcan İ, Berker E. Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia. Odontology. 2021 Apr;109(2):474-482. doi: 10.1007/s10266-020-00565-1. Epub 2020 Nov 7. PubMed PMID: 33159599.

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Acar B, Cagdas D, Tan Ç, Özbek B, Yaz İ, Yıldırım YD, Özşin-Özler C, Karaatmaca B, Gür-Çetinkaya P, Soyak E, Karabulut E, Tezcan İ, Berker E. Correction to: Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia. Odontology. 2021 Apr;109(2):483. doi: 10.1007/s10266-020-00574-0. PubMed PMID: 33377171.

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Cagdas D. Convalescent plasma and hyperimmune globulin therapy in COVID-19. Expert Rev Clin Immunol. 2021 Apr;17(4):309-316. doi: 10.1080/1744666X.2021.1894927. Epub 2021 Mar 12. Review. PubMed PMID: 33620014.

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Soyak Aytekin E, Çağdaş D, Tan C, Tezcan İ. Characteristics of patients with C1 esterase inhibitor deficiency: a single center study. Eur Ann Allergy Clin Immunol. 2021 Mar;53(2):75-79. doi: 10.23822/EurAnnACI.1764-1489.146. Epub 2021 Mar 1. PubMed PMID: 32351099.

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Çağdaş D. Living the SARS-CoV-2 pandemic in Turkey. Nat Immunol. 2021 Mar;22(3):260. doi: 10.1038/s41590-021-00887-4. PubMed PMID: 33627882.

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Soyak Aytekin E, Serin O, Cagdas D, Tan C, Aksu T, Unsal Y, Yeni S, Orhan D, Ozon ZA, Tezcan I. A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess. Pediatr Infect Dis J. 2021 Jan;40(1):66-69. doi: 10.1097/INF.0000000000002887. PubMed PMID: 33284251.

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Aytekin ES, Çağdaş D, Tan Ç, Çavdarlı B, Bilgiç I, Tezcan İ. Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency. Turk J Pediatr. 2021;63(6):1072-1077. doi: 10.24953/turkjped.2021.06.016. PubMed PMID: 35023658.

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Firtina S, Yin Ng Y, Hatirnaz Ng O, Kiykim A, Aydiner E, Nepesov S, Camcioglu Y, Sayar EH, Reisli I, Torun SH, Cogurlu T, Uygun D, Simsek IE, Kaya A, Cipe F, Cagdas D, Yucel E, Cekic S, Uygun V, Baris S, Ozen A, Ozbek U, Sayitoglu M. Mutational landscape of severe combined immunodeficiency patients from Turkey. Int J Immunogenet. 2020 Dec;47(6):529-538. doi: 10.1111/iji.12496. Epub 2020 May 22. PubMed PMID: 32445296.

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Çağdaş D, Pehlivantürk Kizılkan M, Tagiyev A, Emiralioğlu N, Keleş A, Yalçın E, Doğru D, Özçelik U, Kiper N, Tezcan İ. Primary Immunodeficiency Disorders in children with Non-Cystic Fibrosis Bronchiectasis. Eur Ann Allergy Clin Immunol. 2020 Nov;52(6):271-276. doi: 10.23822/EurAnnACI.1764-1489.151. Epub 2020 Nov 3. PubMed PMID: 32372587.

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Cetinkaya PG, Cagdas D, Gumruk F, Tezcan I. Hemophagocytic Lymphohistiocytosis in Patients With Primary Immunodeficiency. J Pediatr Hematol Oncol. 2020 Aug;42(6):e434-e439. doi: 10.1097/MPH.0000000000001803. PubMed PMID: 32324696.

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Cetinkaya PG, Cagdas D, Arikoglu T, Gumruk F, Tezcan I. Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency. J Pediatr Endocrinol Metab. 2020 Jul 28;33(7):957-961. doi: 10.1515/jpem-2019-0541. PubMed PMID: 32623377.

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Altintas B, Cagdas D, van Leeuwen K, de Boer M, Roos D, Tezcan İ. Recurrent skin abscesses in a female X-linked chronic granulomatous disease carrier. J Cosmet Dermatol. 2020 Jul;19(7):1810-1812. doi: 10.1111/jocd.13351. Epub 2020 Mar 10. PubMed PMID: 32154974.

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Solmaz I, Aytekin ES, Çağdaş D, Tan C, Tezcan I, Gocmen R, Haliloglu G, Anlar B. Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency. Neuropediatrics. 2020 Jun;51(3):206-210. doi: 10.1055/s-0039-3399583. Epub 2019 Nov 21. PubMed PMID: 31752029.

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Çağdaş D, Sürücü N, Tan Ç, Kayaoğlu B, Özgül RK, Akkaya-Ulum YZ, Aydınoğlu AT, Aytaç S, Gümrük F, Balci-Hayta B, Balci-Peynircioğlu B, Özen S, Gürsel M, Tezcan İ. Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect. Mol Immunol. 2020 May;121:28-37. doi: 10.1016/j.molimm.2020.02.014. Epub 2020 Mar 6. PubMed PMID: 32151906.

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Dogru D, Polat SE, Tan Ç, Tezcan İ, Yalçın SS, Utine E, Oğuz B, Yaz İ, Emiralioğlu N, Hızal M, Yalçın E, Özçelik U, Çağdaş D, Kiper N. Impact of mannose-binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children. Pediatr Pulmonol. 2020 May;55(5):1190-1198. doi: 10.1002/ppul.24711. Epub 2020 Mar 2. PubMed PMID: 32119194.

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Karaatmaca B, Cagdas D, Tan Ç, Aytaç S, Özbek B, Üner A, Gümrük F, Tezcan İ. A rare form of congenital neutropenia: VPS45 deficiency. Scand J Immunol. 2020 May;91(5):e12871. doi: 10.1111/sji.12871. Epub 2020 Feb 27. PubMed PMID: 32037586.

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Yaz I, Ozbek B, Ng YY, Cetinkaya PG, Halacli SO, Tan C, Kasikci M, Kosukcu C, Tezcan I, Cagdas D. Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study. J Clin Immunol. 2020 Apr;40(3):494-502. doi: 10.1007/s10875-020-00761-2. Epub 2020 Feb 14. PubMed PMID: 32056073.

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Sönmez HE, Karaaslan C, de Jesus AA, Batu ED, Anlar B, Sözeri B, Bilginer Y, Karaguzel D, Cagdas Ayvaz D, Tezcan I, Goldbach-Mansky R, Ozen S. A clinical score to guide in decision making for monogenic type I IFNopathies. Pediatr Res. 2020 Mar;87(4):745-752. doi: 10.1038/s41390-019-0614-2. Epub 2019 Oct 22. PubMed PMID: 31641281; PubMed Central PMCID: PMC8425764.

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Özen S, Batu ED, Taşkıran EZ, Özkara HA, Ünal Ş, Güleray N, Erden A, Karadağ Ö, Gümrük F, Çetin M, Sönmez HE, Bilginer Y, Ayvaz DÇ, Tezcan I. A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2. J Rheumatol. 2020 Jan;47(1):117-125. doi: 10.3899/jrheum.181384. Epub 2019 May 1. PubMed PMID: 31043544.

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Ozbek B, Ayvaz DÇ, Esenboga S, Halaçlι SO, Aytekin ES, Yaz I, Tan Ç, Tezcan I. In case of recurrent wheezing and bronchiolitis: Think again, it may be a primary immunodeficiency. Asian Pac J Allergy Immunol. 2019 Dec 14;. doi: 10.12932/AP-260719-0610. [Epub ahead of print] PubMed PMID: 31837214.



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