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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
2002 1
2003 5
2004 6
2005 3
2006 1
2007 2
2008 1
2009 2
2010 2
2011 2
2012 3
2013 1
2014 1
2015 1
2016 2
2017 3
2018 5
2019 1
2020 2
2021 1
2022 6
2023 3
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49 results
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Page 1
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
Van de Vondel L, De Winter J, Beijer D, Coarelli G, Wayand M, Palvadeau R, Pauly MG, Klein K, Rautenberg M, Guillot-Noël L, Deconinck T, Vural A, Ertan S, Dogu O, Uysal H, Brankovic V, Herzog R, Brice A, Durr A, Klebe S, Stock F, Bischoff AT, Rattay TW, Sobrido MJ, De Michele G, De Jonghe P, Klopstock T, Lohmann K, Zanni G, Santorelli FM, Timmerman V, Haack TB, Züchner S; PREPARE Consortium; Schüle R, Stevanin G, Synofzik M, Basak AN, Baets J. Van de Vondel L, et al. Among authors: dogu o. Mov Disord. 2022 Jun;37(6):1175-1186. doi: 10.1002/mds.28959. Epub 2022 Feb 12. Mov Disord. 2022. PMID: 35150594
Future Prospects in Parkinson's Disease Diagnosis and Treatment.
Öksüz N, Öztürk Ş, Doğu O. Öksüz N, et al. Among authors: dogu o. Noro Psikiyatr Ars. 2022 Dec 16;59(Suppl 1):S36-S41. doi: 10.29399/npa.28169. eCollection 2022. Noro Psikiyatr Ars. 2022. PMID: 36578989 Free PMC article. Review.
Patients with Lately Diagnosed Cerebrotendinous Xanthomatosis.
Yunisova G, Tufekcioglu Z, Dogu O, Bilgic B, Kaleagasi H, Akca Kalem S, Lohmann E, Gurvit HI, Emre M, Hanagasi HA. Yunisova G, et al. Among authors: dogu o. Neurodegener Dis. 2019;19(5-6):218-224. doi: 10.1159/000506770. Epub 2020 Apr 29. Neurodegener Dis. 2019. PMID: 32349000
LRRK2 mutations are uncommon in Turkey.
Hanagasi HA, Lohmann E, Dursun B, Honoré A, Lesage S, Dogu O, Kaleagasi H, Aydın O, Gürvit H, Erginel-Unaltuna N, Brice A, Emre M. Hanagasi HA, et al. Among authors: dogu o. Eur J Neurol. 2011 Oct;18(10):e137. doi: 10.1111/j.1468-1331.2011.03471.x. Eur J Neurol. 2011. PMID: 21914047 No abstract available.
49 results