학술논문

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발행년	- (예 : 2010-2015)

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice

Academic Journal

Vural, A.; Öztop Çakmak, Ö.; Altıntaş, A.; Ertan, S.; Şimşir, G.; Tekgül, Ş.; Gül, T.; Bayraktar, E.; Palvadeau, R.; Tunca, C.; Pirkevi Çetinkaya, C.; Şahbaz, I.; Kovancılar Koç, M.; Başak, A.N.; Koçoğlu, C.; Akçimen, F.; Kartal, E.; Şen, N.E.; Lahut, S.; Ömür, Ö.; Saner, N.; Gündoğdu Eken, A.; Hanağası, H.; Bilgiç, B.; Eraksoy, M.; Parman, Y.; Oflazer, P.; Deymeer, F.; Durmuş, H.; Şahin, E.; Çakar, A.; Tüfekçioğlu, Z.; Gündüz, A.; Apaydın, H.; Kızıltan, G.; Özekmekçi, S.; Siva, A.; Kaya Güleç, Z.E.; Tektürk, P.; Çorbalı, M.O.; Tireli, H.; Akdal, G.; Yiş, U.; Hız, S.; Şengün, İ.; Bora, E.; Serdaroğlu, G.; Erer Özbek, S.; Ağan, K.; İnce Günal, D.; Us, Ö.; Kurt, S.G.; Aksoy, D.; Bora Tokçaer, A.; Elmas, M.; Gültekin, M.; Kumandaş, S.; Acer, H.; Kaya Özçora, G.D.; Yayla, V.; Soysal, A.; Genç, G.; Güllüoğlu, H.; Kotan, D.; Özözen Ayas, Z.; Şahin, H.A.; Tan, E.; Topçu, M.; Topçuoğlu, E.S.; Elibol, B.; Akbostancı, C.; Koç, F.

In: Movement Disorders. (Movement Disorders, July 2021, 36(7):1676-1688)

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Phenotypic and genotypic features of patients diagnosed with ALS in the city of Sakarya, Turkey

Academic Journal

Kotan, D.; Özözen Ayas, Z.; Tunca, C.; Başak, A.N.; Gungen, B.D.; Akçimen, F.

In: Acta Neurologica Belgica. (Acta Neurologica Belgica, 1 December 2020, 120(6):1411-1418)

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An unusual recurrence of miller fisher syndrome: Three times in eight years

Academic Journal

Özözen Ayas, Z.; Güzey Aras, Y.; Doğan Güngen, B.

In: Noropsikiyatri Arsivi. (Noropsikiyatri Arsivi, March 2020, 57(1):78-79)

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Serum prolidase enzyme activity level: Not a predictive biomarker for epilepsy

Academic Journal

Ozozen Ayas, Z.; Kotan, D.; Akdogan, M.; Gunel, M.E.

In: Eurasian Journal of Medicine. (Eurasian Journal of Medicine, February 2019, 51(1):27-30)

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A rare cause of headache: Rathke cleft cyst

Academic Journal

Özözen Ayas, Z.; Asil, K.

In: Erciyes Medical Journal. (Erciyes Medical Journal, March 2018, 40(1):39-41)

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Clinical effect of a mutation (p.glu322asp, c.966 g>t) in pank2 gene in a family with atypical pantothenate kinase-associated neurodegeneration

Academic Journal

Ozozen Ayas, Z.; Karkucak, M.; Oncel Ocal, R.; Yakut, T.

In: Genetic Counseling. (Genetic Counseling, 2016, 27(4):489-494)

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Cerebral fat embolism diagnosed by cognitive disorder

Academic Journal

Kotan, D.; Ozozen Ayas, Z.; Sayan, S.; Atilgan Acar, B.; Inanmaz, M.E.

In: Eurasian Journal of Medicine. (Eurasian Journal of Medicine, June 2014, 46(2):135-137)

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Akinetic mutism following bilateral anterior cerebral artery territory infarction due to aneurysm: A case report

Academic Journal

Özözen Ayas, Z.; Asil, K.; Aksoy, Y.E.

In: Turk Beyin Damar Hastaliklar Dergisi. (Turk Beyin Damar Hastaliklar Dergisi, 2014, 20(1):32-35)

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Fabry disease diagnosis in a young stroke patient: A case report

Academic Journal

Aksoy Gündoğdu, A.; Kotan, D.; Alemdar, M.; Özözen Ayas, Z.

In: Noropsikiyatri Arsivi. (Noropsikiyatri Arsivi, September 2018, 55(3):291-292)

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