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

Year Number of Results
1996 1
2003 1
2004 1
2005 8
2006 4
2007 3
2008 2
2009 2
2010 1
2011 1
2012 2
2013 2
2014 6
2015 4
2016 5
2017 8
2018 3
2019 3
2020 8
2021 4
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59 results
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Page 1
Is training for informal caregivers and their older persons helpful? A systematic review.
Aksoydan E, Aytar A, Blazeviciene A, van Bruchem-Visser RL, Vaskelyte A, Mattace-Raso F, Acar S, Altintas A, Akgun-Citak E, Attepe-Ozden S, Baskici C, Kav S, Kiziltan G. Aksoydan E, et al. Among authors: kiziltan g. Arch Gerontol Geriatr. 2019 Jul-Aug;83:66-74. doi: 10.1016/j.archger.2019.02.006. Epub 2019 Mar 25. Arch Gerontol Geriatr. 2019. PMID: 30953963
Challenges and needs of informal caregivers in elderly care: Qualitative research in four European countries, the TRACE project.
Akgun-Citak E, Attepe-Ozden S, Vaskelyte A, van Bruchem-Visser RL, Pompili S, Kav S, Acar S, Aksoydan E, Altintas A, Aytar A, Baskici C, Blazeviciene A, Scarpa AR, Kiziltan G, Mattace-Raso FUS. Akgun-Citak E, et al. Among authors: kiziltan g. Arch Gerontol Geriatr. 2020 Mar-Apr;87:103971. doi: 10.1016/j.archger.2019.103971. Epub 2019 Nov 5. Arch Gerontol Geriatr. 2020. PMID: 31756568
Genetic variants of vitamin D metabolism-related DHCR7/NADSYN1 locus and CYP2R1 gene are associated with clinical features of Parkinson's disease.
Alaylıoğlu M, Dursun E, Genç G, Şengül B, Bilgiç B, Gündüz A, Apaydın H, Kızıltan G, Gürvit H, Hanağası H, Öztop Çakmak Ö, Ertan S, Yılmazer S, Gezen-Ak D. Alaylıoğlu M, et al. Among authors: kiziltan g. Int J Neurosci. 2020 Sep 16:1-11. doi: 10.1080/00207454.2020.1820502. Online ahead of print. Int J Neurosci. 2020. PMID: 32938288
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.
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.
59 results
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