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

Year Number of Results
2005 1
2006 2
2010 1
2012 3
2014 1
2015 1
2016 1
2017 1
2018 2
2022 0
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Page 1
Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.
Hamilton EMC, Tekturk P, Cialdella F, van Rappard DF, Wolf NI, Yalcinkaya C, Çetinçelik Ü, Rajaee A, Kariminejad A, Paprocka J, Yapici Z, Bošnjak VM, van der Knaap MS; MLC Research Group. Hamilton EMC, et al. Among authors: cetincelik u. Neurology. 2018 Apr 17;90(16):e1395-e1403. doi: 10.1212/WNL.0000000000005334. Epub 2018 Mar 21. Neurology. 2018. PMID: 29661901 Free PMC article.
A case of hereditary hypotrichosis simplex.
Koslu A, Ekmekci TR, Cetincelik U. Koslu A, et al. Among authors: cetincelik u. J Eur Acad Dermatol Venereol. 2006 Oct;20(9):1150-1. doi: 10.1111/j.1468-3083.2006.01646.x. J Eur Acad Dermatol Venereol. 2006. PMID: 16987285 No abstract available.
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Malone AF, Phelan PJ, Hall G, Cetincelik U, Homstad A, Alonso AS, Jiang R, Lindsey TB, Wu G, Sparks MA, Smith SR, Webb NJ, Kalra PA, Adeyemo AA, Shaw AS, Conlon PJ, Jennette JC, Howell DN, Winn MP, Gbadegesin RA. Malone AF, et al. Among authors: cetincelik u. Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17. Kidney Int. 2014. PMID: 25229338 Free PMC article.
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations.
Colombo EA, Bazan JF, Negri G, Gervasini C, Elcioglu NH, Yucelten D, Altunay I, Cetincelik U, Teti A, Del Fattore A, Luciani M, Sullivan SK, Yan AC, Volpi L, Larizza L. Colombo EA, et al. Among authors: cetincelik u. Orphanet J Rare Dis. 2012 Jan 23;7:7. doi: 10.1186/1750-1172-7-7. Orphanet J Rare Dis. 2012. PMID: 22269211 Free PMC article.
12 results