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Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency.
Rosain J, Kiykim A, Michev A, Kendir-Demirkol Y, Rinchai D, Peel JN, Li H, Ocak S, Ozdemir PG, Le Voyer T, Philippot Q, Khan T, Neehus AL, Migaud M, Soudée C, Boisson-Dupuis S, Marr N, Borghesi A, Casanova JL, Bustamante J. Rosain J, et al. Among authors: ocak s. J Clin Immunol. 2024 Feb 16;44(3):62. doi: 10.1007/s10875-024-01661-5. J Clin Immunol. 2024. PMID: 38363432 Free PMC article.
Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic.
Aydemir S, Ocak S, Saygılı S, Hopurcuoğlu D, Haşlak F, Kıykım E, Aktuğlu Zeybek Ç, Celkan T, Demirgan EB, Kasapçopur Ö, Çokuğraş H, Kıykım A, Canpolat N. Aydemir S, et al. Among authors: ocak s. Telemed J E Health. 2021 Oct;27(10):1180-1187. doi: 10.1089/tmj.2020.0381. Epub 2020 Dec 9. Telemed J E Health. 2021. PMID: 33301373
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations.
Thalhammer J, Kindle G, Nieters A, Rusch S, Seppänen MRJ, Fischer A, Grimbacher B, Edgar D, Buckland M, Mahlaoui N, Ehl S; European Society for Immunodeficiencies Registry Working Party. Thalhammer J, et al. J Allergy Clin Immunol. 2021 Nov;148(5):1332-1341.e5. doi: 10.1016/j.jaci.2021.04.015. Epub 2021 Apr 23. J Allergy Clin Immunol. 2021. PMID: 33895260 Free article.
Neurofibromatosis Type 1 in Children: A Single-Center Experience.
Gonca Kaçar A, Kılınc Oktay B, Çınar Özel S, Ocak S, Güneş N, Uludağ Alkaya D, Tüysüz B, Apak H, Tiraje Celkan T. Gonca Kaçar A, et al. Among authors: ocak s. Turk Arch Pediatr. 2021 Jul 1;56(4):339-343. doi: 10.5152/TurkArchPediatr.2021.20165. eCollection 2021 Jul. Turk Arch Pediatr. 2021. PMID: 35005728 Free PMC article.
134 results