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Year Number of Results
2015 1
2018 3
2019 1
2020 3
2021 5
2022 2
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Page 1
Vestibulo-ocular reflex impairment in SPG7 hereditary spastic paraplegia.
Akdal G, Koçoğlu K, Koçoğlu C, Bora E, Nazlı Başak A, Michael Halmágyi G. Akdal G, et al. Among authors: kocoglu c. Clin Neurophysiol. 2021 Jan;132(1):77-79. doi: 10.1016/j.clinph.2020.10.012. Epub 2020 Nov 4. Clin Neurophysiol. 2021. PMID: 33248435 No abstract available.
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers.
Koçoğlu C, Gossye H, Dillen L, Van Mossevelde S, De Bleecker JL, Vandenberghe R, De Deyn PP, Sleegers K, Cras P, Engelborghs S, Van Broeckhoven C, van der Zee J; BELNEU Consortium. Koçoğlu C, et al. Neurobiol Aging. 2021 Jan;97:145.e1-145.e4. doi: 10.1016/j.neurobiolaging.2020.07.021. Epub 2020 Aug 15. Neurobiol Aging. 2021. PMID: 32921502 Free article.
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
Vural A, Şimşir G, Tekgül Ş, Koçoğlu C, Akçimen F, Kartal E, Şen NE, Lahut S, Ömür Ö, Saner N, Gül T, Bayraktar E, Palvadeau R, Tunca C, Pirkevi Çetinkaya C, Gündoğdu Eken A, Şahbaz I, Kovancılar Koç M, Öztop Çakmak Ö, Hanağası H, Bilgiç B, Eraksoy M, Gündüz A, Apaydın H, Kızıltan G, Özekmekçi S, Siva A, Altıntaş A, Kaya Güleç ZE, Parman Y, Oflazer P, Deymeer F, Durmuş H, Şahin E, Çakar A, Tüfekçioğlu Z, Tektürk P, Çorbalı MO, 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 SG, Aksoy D, Bora Tokçaer A, Elmas M, Gültekin M, Kumandaş S, Acer H, Kaya Özçora GD, Yayla V, Soysal A, Genç G, Güllüoğlu H, Kotan D, Özözen Ayas Z, Şahin HA, Tan E, Topçu M, Topçuoğlu ES, Akbostancı C, Koç F, Ertan S, Elibol B, Başak AN. Vural A, et al. Among authors: kocoglu c. Mov Disord. 2021 Jul;36(7):1676-1688. doi: 10.1002/mds.28518. Epub 2021 Feb 24. Mov Disord. 2021. PMID: 33624863
Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families.
Kocoglu C, Gundogdu A, Kocaman G, Kahraman-Koytak P, Uluc K, Kiziltan G, Caglayan AO, Bilguvar K, Vural A, Basak AN. Kocoglu C, et al. Neurol Genet. 2018 Jan 18;4(1):e218. doi: 10.1212/NXG.0000000000000218. eCollection 2018 Feb. Neurol Genet. 2018. PMID: 29379883 Free PMC article. No abstract available.
Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis.
van der Zee J, Dillen L, Baradaran-Heravi Y, Gossye H, Koçoğlu C, Cuyt I, Dermaut B, Sieben A, Baets J, De Jonghe P, Vandenberghe R, De Deyn P, Cras P, Engelborghs S, Van Broeckhoven C; BELNEU Consortium. van der Zee J, et al. Among authors: kocoglu c. Neurobiol Dis. 2021 Aug;156:105421. doi: 10.1016/j.nbd.2021.105421. Epub 2021 Jun 9. Neurobiol Dis. 2021. PMID: 34118419 Free article.
Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene.
Benussi L, Longobardi A, Kocoglu C, Carrara M, Bellini S, Ferrari C, Nicsanu R, Saraceno C, Bonvicini C, Fostinelli S, Zanardini R, Catania M, Moisse M, Van Damme P, Di Fede G, Binetti G, Van Broeckhoven C, van der Zee J, Ghidoni R. Benussi L, et al. Among authors: kocoglu c. Int J Mol Sci. 2021 Dec 20;22(24):13633. doi: 10.3390/ijms222413633. Int J Mol Sci. 2021. PMID: 34948429 Free PMC article.
12 results