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

Year Number of Results
2006 2
2007 1
2008 1
2009 3
2010 2
2011 3
2012 1
2013 8
2014 3
2015 4
2016 14
2017 6
2018 4
2019 2
2020 5
2021 2
2022 3
2023 0
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55 results
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Page 1
Availability of Fibrinogen/Albumin ratio in MS attack.
Çiçekli E, Sayan S, Kotan D. Çiçekli E, et al. Among authors: kotan d. Mult Scler Relat Disord. 2022 Apr;60:103674. doi: 10.1016/j.msard.2022.103674. Epub 2022 Feb 6. Mult Scler Relat Disord. 2022. PMID: 35290899
The role of Orexin-A levels in epileptic seizure.
Çikriklar HI, Kotan D, Yücel M, Ceylan M, Çiftçi GG, Bayraktutan ÖF, Çiftçi IH. Çikriklar HI, et al. Among authors: kotan d. Neurosci Lett. 2020 Aug 24;734:135097. doi: 10.1016/j.neulet.2020.135097. Epub 2020 May 30. Neurosci Lett. 2020. PMID: 32485288
The Turkish experience of COVID-19 infection in people with NMOSD and MOGAD: A milder course?
Sen S, Tuncer A, Ozakbas S, Uzunkopru C, Baba C, Demir S, Beckmann Y, Gumus H, Arslan G, Kilic AK, Altintas A, Yuceyar N, Turan OF, Tutuncu M, Terzi M, Acar P, Bunul SD, Balci BP, Bir LS, Koseoglu M, Mungan S, Gunduz T, Dogan IG, Kotan D, Uygunoglu U, Ekmekci O, Demirkiran M, Kamisli O, Kabay SC, Tamam Y, Omerhoca S, Sevim S, Guler S, Kurtuncu M, Efendi H, Karabudak R, Siva A. Sen S, et al. Among authors: kotan d. Mult Scler Relat Disord. 2022 Feb;58:103399. doi: 10.1016/j.msard.2021.103399. Epub 2021 Nov 19. Mult Scler Relat Disord. 2022. PMID: 35216782 Free PMC 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: kotan d. Mov Disord. 2021 Jul;36(7):1676-1688. doi: 10.1002/mds.28518. Epub 2021 Feb 24. Mov Disord. 2021. PMID: 33624863
Osmophobia and olfactory functions in patients with migraine.
Kayabaşoglu G, Altundag A, Kotan D, Dizdar D, Kaymaz R. Kayabaşoglu G, et al. Among authors: kotan d. Eur Arch Otorhinolaryngol. 2017 Feb;274(2):817-821. doi: 10.1007/s00405-016-4283-z. Epub 2016 Aug 30. Eur Arch Otorhinolaryngol. 2017. PMID: 27577041
A Turkish Family with a Familial ALS-positive UBQLN2-S340I Mutation.
Kotan D, Iskender C, Özoğuz Erimiş A, Başak AN. Kotan D, et al. Noro Psikiyatr Ars. 2016 Sep;53(3):283-285. doi: 10.5152/npa.2016.12371. Epub 2016 Sep 1. Noro Psikiyatr Ars. 2016. PMID: 28373810 Free PMC article. No abstract available.
A rare neurologic deficiency in HaNDL syndrome: cranial neuropathy.
Kotan D, Sayan S, Koksal SA. Kotan D, et al. Arch Med Sci Atheroscler Dis. 2016 Jun 22;1(1):e49-e52. doi: 10.5114/amsad.2016.60799. eCollection 2016. Arch Med Sci Atheroscler Dis. 2016. PMID: 28905019 Free PMC article. No abstract available.
55 results