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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 8
2017 4
2018 3
2019 3
2020 7
2021 6
2022 8
2023 7
2024 3

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107 results

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Page 1
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.
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
Rhombencephalosynapsis: clinical findings and neuroimaging in 9 children.
Toelle SP, Yalcinkaya C, Kocer N, Deonna T, Overweg-Plandsoen WC, Bast T, Kalmanchey R, Barsi P, Schneider JF, Capone Mori A, Boltshauser E. Toelle SP, et al. Among authors: yalcinkaya c. Neuropediatrics. 2002 Aug;33(4):209-14. doi: 10.1055/s-2002-34498. Neuropediatrics. 2002. PMID: 12368992 Review.
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
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.
Long-Term Disease Course of Pontocerebellar Hypoplasia Type 10.
Guler S, Aslanger AD, Uygur Sahin T, Alkan A, Yalcinkaya C, Saltik S, Yesil G. Guler S, et al. Among authors: yalcinkaya c. Pediatr Neurol. 2024 Jun 6;158:1-10. doi: 10.1016/j.pediatrneurol.2024.05.017. Online ahead of print. Pediatr Neurol. 2024. PMID: 38925092
Prenatal diagnosis of McKusick-Kaufman/Bardet-Biedl syndrome.
Parlakgumus A, Yalcinkaya C, Kilicdag E. Parlakgumus A, et al. Among authors: yalcinkaya c. BMJ Case Rep. 2011 Mar 24;2011:bcr0220113808. doi: 10.1136/bcr.02.2011.3808. BMJ Case Rep. 2011. PMID: 22699466 Free PMC article.
107 results