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Results by year

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

Year Number of Results
1877 2
1905 1
1945 2
1962 3
1968 2
1969 2
1971 1
1973 2
1974 1
1975 2
1976 4
1977 3
1978 9
1979 5
1980 11
1981 9
1982 15
1983 7
1984 18
1985 12
1986 7
1987 13
1988 15
1989 16
1990 3
1991 13
1992 10
1993 8
1994 4
1995 11
1996 7
1997 4
1998 6
1999 9
2000 5
2001 11
2002 7
2003 7
2004 5
2005 11
2006 20
2007 20
2008 17
2009 15
2010 10
2011 12
2012 13
2013 16
2014 13
2015 18
2016 22
2017 18
2018 13
2019 12
2020 14
2021 17
2022 12
2023 4
Text availability
Article attribute
Article type
Publication date

Search Results

520 results
Results by year
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Page 1
Neurobiology of Photophobia.
Burstein R, Noseda R, Fulton AB. Burstein R, et al. Among authors: fulton ab. J Neuroophthalmol. 2019 Mar;39(1):94-102. doi: 10.1097/WNO.0000000000000766. J Neuroophthalmol. 2019. PMID: 30762717 Free PMC article. Review.
ISCEV guide to visual electrodiagnostic procedures.
Robson AG, Nilsson J, Li S, Jalali S, Fulton AB, Tormene AP, Holder GE, Brodie SE. Robson AG, et al. Among authors: fulton ab. Doc Ophthalmol. 2018 Feb;136(1):1-26. doi: 10.1007/s10633-017-9621-y. Epub 2018 Feb 3. Doc Ophthalmol. 2018. PMID: 29397523 Free PMC article.
Kearns-Sayre Syndrome Masquerading as Myasthenia Gravis.
Sokol JT, Hoyek S, Fulton AB, Patel NA. Sokol JT, et al. Among authors: fulton ab. Retin Cases Brief Rep. 2022 Dec 22. doi: 10.1097/ICB.0000000000001397. Online ahead of print. Retin Cases Brief Rep. 2022. PMID: 36729003
Juvenile Macular Degenerations.
Altschwager P, Ambrosio L, Swanson EA, Moskowitz A, Fulton AB. Altschwager P, et al. Among authors: fulton ab. Semin Pediatr Neurol. 2017 May;24(2):104-109. doi: 10.1016/j.spen.2017.05.005. Epub 2017 May 23. Semin Pediatr Neurol. 2017. PMID: 28941524 Free PMC article. Review.
iPSC modeling of young-onset Parkinson's disease reveals a molecular signature of disease and novel therapeutic candidates.
Laperle AH, Sances S, Yucer N, Dardov VJ, Garcia VJ, Ho R, Fulton AN, Jones MR, Roxas KM, Avalos P, West D, Banuelos MG, Shu Z, Murali R, Maidment NT, Van Eyk JE, Tagliati M, Svendsen CN. Laperle AH, et al. Among authors: fulton an. Nat Med. 2020 Feb;26(2):289-299. doi: 10.1038/s41591-019-0739-1. Epub 2020 Jan 27. Nat Med. 2020. PMID: 31988461
Albinism.
McHam ML, Fulton A. McHam ML, et al. Among authors: fulton a. Int Ophthalmol Clin. 1992 Winter;32(1):185-200. doi: 10.1097/00004397-199203210-00015. Int Ophthalmol Clin. 1992. PMID: 1537658 Review. No abstract available.
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing.
Consugar MB, Navarro-Gomez D, Place EM, Bujakowska KM, Sousa ME, Fonseca-Kelly ZD, Taub DG, Janessian M, Wang DY, Au ED, Sims KB, Sweetser DA, Fulton AB, Liu Q, Wiggs JL, Gai X, Pierce EA. Consugar MB, et al. Among authors: fulton ab. Genet Med. 2015 Apr;17(4):253-261. doi: 10.1038/gim.2014.172. Epub 2014 Nov 20. Genet Med. 2015. PMID: 25412400 Free PMC article.
520 results