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Page 1
ATP8A2-related disorders as recessive cerebellar ataxia.
Guissart C, Harrison AN, Benkirane M, Oncel I, Arslan EA, Chassevent AK, Baraῆano K, Larrieu L, Iascone M, Tenconi R, Claustres M, Eroglu-Ertugrul N, Calvas P, Topaloglu H, Molday RS, Koenig M. Guissart C, et al. Among authors: arslan ea. J Neurol. 2020 Jan;267(1):203-213. doi: 10.1007/s00415-019-09579-4. Epub 2019 Oct 14. J Neurol. 2020. PMID: 31612321 Free article.
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.
Bektaş Ö, Gülşen M, Dursun OB, Tekin A, Yüksel D, Demir E, Öztürk G, Saltık S, Hergüler Ö, Özçelik AA, Tan H, Özgör B, Ekici A, Yüksel MF, Şahin S, Duman Ö, Kömür M, Baydan F, Yıldız EP, Kara B, Yiş U, Kanmaz S, Çarman KB, Arslan EA, Canpolat M, Güven AS, Öztuncer G, Ünalp A, Ardıçlı D, Karaduman AA, Zararsız G, Deda G; Turkish SMA Study Group. Bektaş Ö, et al. Among authors: arslan ea. Front Neurol. 2025 Mar 27;16:1541507. doi: 10.3389/fneur.2025.1541507. eCollection 2025. Front Neurol. 2025. PMID: 40212617 Free PMC article.
Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.
Öz Tunçer G, Sanri A, Aydin S, Hergüner ÖM, Özgün N, Kömür M, İçağasioğlu DF, Toker RT, Yilmaz S, Arslan EA, Güngör M, Kutluk G, Erol İ, Mert GG, Polat BG, Aksoy A. Öz Tunçer G, et al. Among authors: arslan ea. J Neuromuscul Dis. 2023;10(5):915-924. doi: 10.3233/JND-230046. J Neuromuscul Dis. 2023. PMID: 37355912 Free PMC article.
HMGB-1, TLR4, IL-1R1, TNF-α, and IL-1β: novel epilepsy markers?
Kamaşak T, Dilber B, Yaman SÖ, Durgut BD, Kurt T, Çoban E, Arslan EA, Şahin S, Karahan SC, Cansu A. Kamaşak T, et al. Among authors: arslan ea. Epileptic Disord. 2020 Apr 1;22(2):183-193. doi: 10.1684/epd.2020.1155. Epileptic Disord. 2020. PMID: 32301731
An investigation of the effects of chronic zonisamide, sultiam, lacosamide, clobazam, and rufinamide anti-seizure medications on foliculogenesis in ovarian tissue in prepubertal non-epileptic rats.
Kart PÖ, Gürgen SG, Esenülkü G, Dilber B, Yıldız N, Yazar U, Sarsmaz HY, Topsakal AS, Kamaşak T, Arslan EA, Şahin S, Cansu A. Kart PÖ, et al. Among authors: arslan ea. Int J Dev Neurosci. 2022 Aug;82(5):436-446. doi: 10.1002/jdn.10200. Epub 2022 Jul 5. Int J Dev Neurosci. 2022. PMID: 35680420
A rare cause of chronic ataxia in childhood: ganglioneuroma.
Arslan EA, Kamaşak T, Turgut BD, Saygın İ, Sarıhan H, Cansu A. Arslan EA, et al. World J Pediatr. 2018 Apr;14(2):204-206. doi: 10.1007/s12519-018-0141-y. Epub 2018 Mar 12. World J Pediatr. 2018. PMID: 29532434 No abstract available.
The effectiveness and tolerability of clobazam in the pediatric population: Adjunctive therapy and monotherapy in a large-cohort multicenter study.
Kamaşak T, Serdaroğlu E, Yılmaz Ö, Kılıç BA, Polat BG, Erdoğan I, Yücel Şen AD, Özen N, Durgut BD, Yıldız N, Özkan Kart P, Dilber B, Arslan EA, Şahin S, Topçu Y, Gencpinar P, Serin HM, Hız SA, Çarman KB, Dündar NO, Okuyaz Ç, Aydın K, Serdaroğlu A, Tekgül H, Cansu A. Kamaşak T, et al. Among authors: arslan ea. Epilepsy Res. 2022 Aug;184:106963. doi: 10.1016/j.eplepsyres.2022.106963. Epub 2022 Jun 6. Epilepsy Res. 2022. PMID: 35749975
27 results