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

Year Number of Results
2003 1
2005 1
2007 2
2009 1
2012 1
2013 1
2014 4
2015 3
2016 4
2017 8
2018 3
2020 4
2021 2
2022 6
2023 3
2024 0

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36 results

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Page 1
ADCY5 gene mutation: a case report.
Tezen D, Gunduz A, Erdemir Kiziltan M, Yalcinkaya C, Kiziltan G. Tezen D, et al. Among authors: kiziltan g. Neurol Sci. 2022 Dec;43(12):6947-6950. doi: 10.1007/s10072-022-06394-0. Epub 2022 Sep 16. Neurol Sci. 2022. PMID: 36112278
Stiff Person Syndrome with Pyramidal Signs.
Nalbantoğlu M, Battal H, Kiziltan ME, Akalin MA, Kiziltan G. Nalbantoğlu M, et al. Among authors: kiziltan g. Noro Psikiyatr Ars. 2016 Jun;53(2):188-190. doi: 10.5152/npa.2015.11310. Epub 2016 Jun 1. Noro Psikiyatr Ars. 2016. PMID: 28360797 Free PMC article. No abstract available.
Recurrent Catatonia in Parkinson Disease.
Poyraz BÇ, Aksoy Poyraz C, Yassa A, Arikan MK, Gündüz A, Kiziltan G. Poyraz BÇ, et al. Among authors: kiziltan g. J Clin Psychopharmacol. 2016 Feb;36(1):104-6. doi: 10.1097/JCP.0000000000000443. J Clin Psychopharmacol. 2016. PMID: 26658081 No abstract available.
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. Among authors: kiziltan g. 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.
36 results