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Page 1
Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiency.
Gul E, Sayar EH, Gungor B, Eroglu FK, Surucu N, Keles S, Guner SN, Findik S, Alpdundar E, Ayanoglu IC, Kayaoglu B, Geckin BN, Sanli HA, Kahraman T, Yakicier C, Muftuoglu M, Oguz B, Cagdas Ayvaz DN, Gursel I, Ozen S, Reisli I, Gursel M. Gul E, et al. Among authors: oguz b. J Allergy Clin Immunol. 2018 Jul;142(1):246-257. doi: 10.1016/j.jaci.2017.10.030. Epub 2017 Nov 16. J Allergy Clin Immunol. 2018. PMID: 29155101
Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.
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. Sener S, et al. Among authors: oguz b. Clin Rheumatol. 2022 Sep;41(9):2883-2892. doi: 10.1007/s10067-022-06295-9. Epub 2022 Jul 20. Clin Rheumatol. 2022. PMID: 35854168 Review.
The risk of cardiovascular comorbidity in children with Behçet's disease.
Demir S, Duzova A, Karagoz T, Oguz B, Aykan HH, Satirer O, Sag E, Ozen S, Bilginer Y. Demir S, et al. Among authors: oguz b. Rheumatology (Oxford). 2024 Sep 1;63(SI2):SI188-SI194. doi: 10.1093/rheumatology/kead505. Rheumatology (Oxford). 2024. PMID: 37788103 Free PMC article.
A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly.
Esenboga S, Çagdas D, Oguz B, Bajin I, Aydin B, Akyuz C, Tezcan I. Esenboga S, et al. Among authors: oguz b. J Pediatr Hematol Oncol. 2018 Apr;40(3):248-251. doi: 10.1097/MPH.0000000000001101. J Pediatr Hematol Oncol. 2018. PMID: 29432311 No abstract available.
Clinical spectrum of children with interstitial pneumonia with autoimmune features.
Ademhan Tural D, Emiralioglu N, Ozsezen B, Sunman B, Nayir Buyuksahin H, Guzelkas I, Oguz B, Bilginer Y, Orhan D, Yalcin E, Dogru D, Ozcelik U, Ozen S, Kiper N. Ademhan Tural D, et al. Among authors: oguz b. Respir Med. 2021 Oct;187:106566. doi: 10.1016/j.rmed.2021.106566. Epub 2021 Aug 12. Respir Med. 2021. PMID: 34416614 Free article.
155 results