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Correction to: A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
Lanz AL, Erdem S, Ozcan A, Ceylaner G, Cansever M, Ceylaner S, Conca R, Magg T, Acuto O, Latour S, Klein C, Patiroglu T, Unal E, Eken A, Hauck F. Lanz AL, et al. Among authors: ceylaner s. J Clin Immunol. 2024 Jan 16;44(1):41. doi: 10.1007/s10875-024-01654-4. J Clin Immunol. 2024. PMID: 38225415 Free PMC article. No abstract available.
Junctional Epidermolysis Bullosa Linked to Homozygous Mutation in LAMC2 Gene: A Case Report With Eosinophil-Rich Inflammatory Infiltrate.
Haskoloğlu Ş, Öztürk G, Deveci Demirbaş N, Akal C, İslamoğlu C, Baskın K, Heper A, Erdeve Ö, Ceylaner S, Doğu F, İkincioğulları A. Haskoloğlu Ş, et al. Among authors: ceylaner s. Am J Dermatopathol. 2024 Apr 23. doi: 10.1097/DAD.0000000000002714. Online ahead of print. Am J Dermatopathol. 2024. PMID: 38648026
Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?
Öztürk G, Haskoloğlu Ş, Deveci N, Erkmen H, Çelik NA, Sucak G, Ceylaner S, İkincioğulları A, Doğu F. Öztürk G, et al. Among authors: ceylaner s. Turk Arch Pediatr. 2023 Sep 22;59(1):106-8. doi: 10.5152/TurkArchPediatr.2023.23157. Online ahead of print. Turk Arch Pediatr. 2023. PMID: 37737227 Free PMC article. No abstract available.
Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study.
Cavusoglu D, Ozturk G, Turkdogan D, Kurul SH, Yis U, Komur M, Incecik F, Kara B, Sahin T, Unver O, Dilber C, Mert GG, Gunay C, Uzan GS, Ersoy O, Oktay Y, Mermer S, Tuncer GO, Gungor O, Ozcora GDK, Gumus U, Sezer O, Cetin GO, Demir F, Yilmaz A, Gurbuz G, Topcu M, Topaloglu H, Ceylan AC, Ceylaner S, Gleeson JG, Icagasioglu DF, Sonmez FM. Cavusoglu D, et al. Among authors: ceylaner s. Cerebellum. 2024 Apr 15. doi: 10.1007/s12311-024-01690-1. Online ahead of print. Cerebellum. 2024. PMID: 38622473
Hb Andrew-Minneapolis Variant in a Turkish Family.
Sümter H, Mızrak S, Ceylaner S, Canatan D. Sümter H, et al. Among authors: ceylaner s. Turk J Haematol. 2023 Aug 31;40(3):234-235. doi: 10.4274/tjh.galenos.2023.2023-0239. Epub 2023 Jul 31. Turk J Haematol. 2023. PMID: 37519109 Free PMC article. No abstract available.
Genetic variants of GBA and GLA in a Turkish cohort of Parkinson's disease: A preliminary report.
Yekedüz MK, Yilmaz R, Kayis G, Doğulu N, Öncül Ü, Abali T, Temizyurek AD, Çelik G, Çöklü H, Gemci E, Yalcin A, Ceylaner S, Akbostancı MC, Eminoğlu FT. Yekedüz MK, et al. Among authors: ceylaner s. Parkinsonism Relat Disord. 2023 May;110:105390. doi: 10.1016/j.parkreldis.2023.105390. Epub 2023 Mar 31. Parkinsonism Relat Disord. 2023. PMID: 37027993 No abstract available.
Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?
Hakan N, Aydin M, Ceylaner S, Dilli D, Zenciroğlu A, Okumuş N. Hakan N, et al. Among authors: ceylaner s. Balkan J Med Genet. 2024 Mar 12;26(2):51-58. doi: 10.2478/bjmg-2023-0021. eCollection 2023 Dec. Balkan J Med Genet. 2024. PMID: 38482260 Free PMC article.
238 results