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Page 1
Exploring shared triggers and potential etiopathogenesis between migraine and idiopathic/genetic epilepsy: Insights from a multicenter tertiary-based study.
Türk BG, Yeni SN, Atalar AÇ, Ekizoğlu E, Gök DK, Baykan B, Özge A, Ayta S, Erdoğan FF, Taşdelen B, Velioğlu SK; IDEM Study Group. Türk BG, et al. Among authors: ayta s. Clin Neurol Neurosurg. 2024 Feb;237:108146. doi: 10.1016/j.clineuro.2024.108146. Epub 2024 Feb 6. Clin Neurol Neurosurg. 2024. PMID: 38367542
An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures.
Yalçin O, Baykan B, Ağan K, Yapici Z, Yalçin D, Dizdarer G, Türkdoğan D, Ozkara C, Unalp A, Uludüz D, Gül G, Kuşcu D, Ayta S, Tutkavul K, Comu S, Tatli B, Meral C, Bebek N, Cağlayan SH. Yalçin O, et al. Among authors: ayta s. Epilepsia. 2011 May;52(5):975-83. doi: 10.1111/j.1528-1167.2010.02970.x. Epub 2011 Feb 14. Epilepsia. 2011. PMID: 21320115 Free article.
Headache in idiopathic/genetic epilepsy: Cluster analysis in a large cohort.
Atalar AÇ, Türk BG, Ekizoglu E, Kurt Gök D, Baykan B, Özge A, Ayta S, Erdoğan FF, Yeni SN, Taşdelen B, Velioglu SK, Yapıcı Z, Midi İ, Saygı S, Çelebi U, Sarıca Darol E, Ağan K, Ayça S, Gazioğlu S, Okudan ZV, Şirin NG, Bebek N, Dericioğlu N, Güçlü Altun İ, Yalçın AD, Sürmeli R, Erdinç OO, Erdal A, İlhan Algın D, Kutlu G, Bek S, Erdal Y, Özön AÖ, Reyhani A, Güldiken B, Baklan B, Genç BO, Aykutlu Altındağ E, Karahan G, Koç G, Mısırlı H, Öztura İ, Aslan-Kara K, Çakar MM, Türkmen N, Bulut O, Karadaş Ö, Kesim Şahin Ö, Ferik S, Peköz MT, Topaloğlu P, Üstün Özek S, Düzgün Ü, Yayla V, Gömceli Y, Ünlüsoy Acar Z. Atalar AÇ, et al. Among authors: ayta s. Epilepsia. 2022 Jun;63(6):1516-1529. doi: 10.1111/epi.17205. Epub 2022 Apr 6. Epilepsia. 2022. PMID: 35188224
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
EPICURE Consortium; Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T. EPICURE Consortium, et al. Epilepsia. 2012 Feb;53(2):308-18. doi: 10.1111/j.1528-1167.2011.03379.x. Epub 2012 Jan 13. Epilepsia. 2012. PMID: 22242659 Free article.
Auditory evoked blink reflex in peripheral facial paresis.
Ayta S, Sohtaoğlu M, Uludüz D, Uygunoğlu U, Tütüncü M, Akalin MA, Kiziltan ME. Ayta S, et al. J Clin Neurophysiol. 2015 Feb;32(1):34-8. doi: 10.1097/WNP.0000000000000121. J Clin Neurophysiol. 2015. PMID: 25159736
Cranial Autonomic Features in Migraine and Migrainous Features in Cluster Headache.
Uluduz D, Ayta S, Özge A, Yalin OÖ; Turkish Headache Database Study Group; Temel GÖ, Taşdelen B. Uluduz D, et al. Among authors: ayta s. Noro Psikiyatr Ars. 2016 Jul 15;55(3):220-224. doi: 10.5152/npa.2016.19183. eCollection 2018 Sep. Noro Psikiyatr Ars. 2016. PMID: 30224867 Free PMC article.
The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.
Haryanyan G, Ozdemir O, Tutkavul K, Dervent A, Ayta S, Ozkara C, Salman B, Yucesan E, Kesim Y, Susgun S, Ozbek U, Baykan B, Ugur Iseri SA, Bebek N. Haryanyan G, et al. Among authors: ayta s. J Hum Genet. 2021 Dec;66(12):1145-1151. doi: 10.1038/s10038-021-00944-8. Epub 2021 Jun 11. J Hum Genet. 2021. PMID: 34117373
16 results