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Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies.
Krüger J, Schubert J, Kegele J, Labalme A, Mao M, Heighway J, Seebohm G, Yan P, Koko M, Aslan-Kara K, Caglayan H, Steinhoff BJ, Weber YG, Keo-Kosal P, Berkovic SF, Hildebrand MS, Petrou S, Krause R, May P, Lesca G, Maljevic S, Lerche H. Krüger J, et al. Among authors: aslan kara k. EBioMedicine. 2022 Oct;84:104244. doi: 10.1016/j.ebiom.2022.104244. Epub 2022 Sep 9. EBioMedicine. 2022. PMID: 36088682 Free PMC 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. Epilepsia. 2022 Jun;63(6):1516-1529. doi: 10.1111/epi.17205. Epub 2022 Apr 6. Epilepsia. 2022. PMID: 35188224
Diagnosis of comorbid migraine without aura in patients with idiopathic/genetic epilepsy based on the gray zone approach to the International Classification of Headache Disorders 3 criteria.
Atalar AÇ, Özge A, Türk BG, Ekizoğlu E, Kurt Gök D, Baykan B, Ayta S, Erdoğan FF, Yeni SN, Taşdelen B; IDEM Study Group; Velioğlu SK. Atalar AÇ, et al. Front Neurol. 2023 Jan 10;13:1103541. doi: 10.3389/fneur.2022.1103541. eCollection 2022. Front Neurol. 2023. PMID: 36703639 Free PMC article.
14 results