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

Year Number of Results
1989 3
1990 1
1995 1
1997 1
1999 2
2000 5
2001 1
2002 2
2003 4
2004 3
2005 4
2006 1
2007 1
2008 3
2009 4
2010 7
2011 7
2012 6
2013 7
2014 7
2015 6
2016 9
2017 4
2018 4
2019 3
2020 7
2021 6
2022 8
2023 7
2024 8

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113 results

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Page 1
Trial of Fingolimod versus Interferon Beta-1a in Pediatric Multiple Sclerosis.
Chitnis T, Arnold DL, Banwell B, Brück W, Ghezzi A, Giovannoni G, Greenberg B, Krupp L, Rostásy K, Tardieu M, Waubant E, Wolinsky JS, Bar-Or A, Stites T, Chen Y, Putzki N, Merschhemke M, Gärtner J; PARADIGMS Study Group. Chitnis T, et al. N Engl J Med. 2018 Sep 13;379(11):1017-1027. doi: 10.1056/NEJMoa1800149. N Engl J Med. 2018. PMID: 30207920 Free article. Clinical Trial.
Ocrelizumab in pediatric multiple sclerosis.
Bibinoğlu Amirov C, Saltık S, Yalçınkaya C, Tütüncü M, Saip S, Siva A, Uygunoğlu U. Bibinoğlu Amirov C, et al. Among authors: yalcinkaya c. Eur J Paediatr Neurol. 2023 Mar;43:1-5. doi: 10.1016/j.ejpn.2023.01.011. Epub 2023 Jan 27. Eur J Paediatr Neurol. 2023. PMID: 36724688
ADCY5 gene mutation: a case report.
Tezen D, Gunduz A, Erdemir Kiziltan M, Yalcinkaya C, Kiziltan G. Tezen D, et al. Among authors: yalcinkaya c. Neurol Sci. 2022 Dec;43(12):6947-6950. doi: 10.1007/s10072-022-06394-0. Epub 2022 Sep 16. Neurol Sci. 2022. PMID: 36112278
MRI and MRS in HMG-CoA lyase deficiency.
Yalçinkaya C, Dinçer A, Gündüz E, Fiçicioğlu C, Koçer N, Aydin A. Yalçinkaya C, et al. Pediatr Neurol. 1999 May;20(5):375-80. doi: 10.1016/s0887-8994(99)00013-2. Pediatr Neurol. 1999. PMID: 10371384 Review.
Hypomyelination and congenital cataract: broadening the clinical phenotype.
Biancheri R, Zara F, Rossi A, Mathot M, Nassogne MC, Yalcinkaya C, Erturk O, Tuysuz B, Di Rocco M, Gazzerro E, Bugiani M, van Spaendonk R, Sistermans EA, Minetti C, van der Knaap MS, Wolf NI. Biancheri R, et al. Among authors: yalcinkaya c. Arch Neurol. 2011 Sep;68(9):1191-4. doi: 10.1001/archneurol.2011.201. Arch Neurol. 2011. PMID: 21911699 Review.
Challenges in diagnosing SSPE.
Erturk O, Karslıgil B, Cokar O, Yapici Z, Demirbilek V, Gurses C, Yalcinkaya C, Gokyigit A, Direskeneli GS, Yentur S, Onal E, Yilmaz G, Dervent A. Erturk O, et al. Among authors: yalcinkaya c. Childs Nerv Syst. 2011 Dec;27(12):2041-4. doi: 10.1007/s00381-011-1603-x. Epub 2011 Oct 15. Childs Nerv Syst. 2011. PMID: 22002104
Progression of myoclonus subtypes in subacute sclerosing panencephalitis.
Ser MH, Gündüz A, Demirbilek V, Yalçınkaya C, Nalbantoğlu M, Coşkun T, Kızıltan M. Ser MH, et al. Among authors: yalcinkaya c. Neurophysiol Clin. 2021 Dec;51(6):533-540. doi: 10.1016/j.neucli.2021.07.001. Epub 2021 Nov 10. Neurophysiol Clin. 2021. PMID: 34772596
Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome.
Caglayan AO, Tuysuz B, Gül E, Alkaya DU, Yalcinkaya C, Gleeson JG, Bilguvar K, Gunel M. Caglayan AO, et al. Among authors: yalcinkaya c. J Hum Genet. 2022 Sep;67(9):553-556. doi: 10.1038/s10038-022-01032-1. Epub 2022 Mar 25. J Hum Genet. 2022. PMID: 35338243 Free PMC article.
113 results