Biblio

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2015

Volk T, Pannicke U, Reisli I, Bulashevska A, Ritter J, Björkman A, Schäffer AA, Fliegauf M, Sayar EH, Salzer U, et al. DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency. Hum Mol Genet. 2015.

2023

Erdem S, Haskoloğlu Ş, Haliloglu Y, Çelikzencir H, Arik E, Keskin O, Eltan SBilgic, Yucel E, Canatan H, Avcilar H, et al. Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1. Clin Immunol. 2023:109691.

Tar I, Szegedi M, Krasuska-Sławińska E, Heropolitańska-Pliszka E, Bernatowska EA, Öncü E, Keles S, Guner SN, Reisli I, Gesheva N, et al. Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome. Cent Eur J Immunol. 2023;48(3):228-236.

Korkmaz SBusra, Karaselek MAli, Aytekin SErol, Tokgoz H, Reisli I, Güner Ş, Keles S. Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20-year single centre experience. Int J Immunogenet. 2023.