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

Year Number of Results
1994 1
1995 1
1997 2
1998 1
1999 3
2000 7
2001 6
2002 4
2003 12
2004 8
2005 9
2006 15
2007 14
2008 19
2009 15
2010 24
2011 22
2012 13
2013 22
2014 40
2015 36
2016 37
2017 29
2018 47
2019 68
2020 48
2021 58
2022 37
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Search Results

509 results
Results by year
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Page 1
The importance of boron in biological systems.
Uluisik I, Karakaya HC, Koc A. Uluisik I, et al. Among authors: koc a. J Trace Elem Med Biol. 2018 Jan;45:156-162. doi: 10.1016/j.jtemb.2017.10.008. Epub 2017 Oct 26. J Trace Elem Med Biol. 2018. PMID: 29173473 Review.
Spinal brucellosis.
Tali ET, Koc AM, Oner AY. Tali ET, et al. Among authors: koc am. Neuroimaging Clin N Am. 2015 May;25(2):233-45. doi: 10.1016/j.nic.2015.01.004. Neuroimaging Clin N Am. 2015. PMID: 25952175 Review.
Pyogenic spinal infections.
Tali ET, Oner AY, Koc AM. Tali ET, et al. Among authors: koc am. Neuroimaging Clin N Am. 2015 May;25(2):193-208. doi: 10.1016/j.nic.2015.01.003. Neuroimaging Clin N Am. 2015. PMID: 25952173 Review.
A toddler with a novel LEPR mutation.
Armağan C, Yılmaz C, Koç A, Abacı A, Ülgenalp A, Böber E, Erçal D, Demir K. Armağan C, et al. Among authors: koc a. Hormones (Athens). 2019 Jun;18(2):237-240. doi: 10.1007/s42000-019-00097-6. Epub 2019 Feb 18. Hormones (Athens). 2019. PMID: 30778850
Brown Syndrome: Features and Long-term Results of Management.
Koc AA, Aygit ED, Inal A, Ocak B, Gurez C, Ahmet S, Duman B, Gokyigit B. Koc AA, et al. Beyoglu Eye J. 2021 Sep 27;6(3):223-228. doi: 10.14744/bej.2021.35693. eCollection 2021. Beyoglu Eye J. 2021. PMID: 35005520 Free PMC article.
A case with bilateral radio-ulnar synostosis.
Koç A, Kaymak AO, Karaer K, Ergün MA, Aksu T, Perçin EF. Koç A, et al. Genet Couns. 2008;19(2):193-8. Genet Couns. 2008. PMID: 18618994 Review.
Deep iterative reconstruction for phase retrieval.
Işıl Ç, Oktem FS, Koç A. Işıl Ç, et al. Among authors: koc a. Appl Opt. 2019 Jul 10;58(20):5422-5431. doi: 10.1364/AO.58.005422. Appl Opt. 2019. PMID: 31504010
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit S, Tozkir H, Yalcintepe S, Ozkayin N, Kiraz A, Balta B, Gonen GA, Kurt EE, Ceylan GG, Ceylan AC, Erten S, Bozdogan ST, Boga I, Yilmaz M, Silan F, Kocabey M, Koc A, Cankaya T, Bora E, Bozkaya OG, Ercal D, Ergun MA, Ergun SG, Duman YS, Beyazit SB, Uzel VH, Em S, Cevik MO, Eroz R, Demirtas M, Firat CK, Kabayegit ZM, Altan M, Mardan L, Sayar C, Tumer S, Turkgenc B, Karakoyun HK, Tunc B, Kuru S, Zamani A, Geckinli BB, Ates EA, Clark OA, Toylu A, Coskun M, Nur B, Bilge I, Bayramicli OU, Emmungil H, Komesli Z, Zeybel M, Gurakan F, Tasdemir M, Kebudi R, Karabulut HG, Tuncali T, Kutlay NY, Kahraman CY, Onder NB, Beyitler I, Kavukcu S, Tulay P, Tosun O, Tuncel G, Mocan G, Kale H, Uyguner ZO, Acar A, Altinay M, Erdem L; National Genetics Consortium Study. Dundar M, et al. Among authors: koc a. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31. Funct Integr Genomics. 2022. PMID: 35098403
509 results