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

Year Number of Results
2003 1
2004 1
2005 2
2006 2
2007 2
2008 3
2009 2
2010 6
2011 6
2012 1
2013 3
2014 7
2015 10
2016 3
2017 6
2018 7
2019 6
2020 5
2021 5
2022 3
2023 4
2024 2

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72 results

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Page 1
Vitreomacular interface abnormalities in the Ghanaian African.
Amoaku WM, Cushley L, Silvestri V, Akafo S, Amissah-Arthur KN, Lartey S, Hageman CN, Pappas CM, Hubbard WC, Bernstein PS, Vitale A, Roberts M, Virgili G, Hageman GS, Silvestri G; Ghana AMD Study Group. Amoaku WM, et al. Among authors: silvestri g. Eye (Lond). 2024 Feb;38(3):578-584. doi: 10.1038/s41433-023-02737-z. Epub 2023 Sep 29. Eye (Lond). 2024. PMID: 37773435 Free PMC article.
Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review.
Stephenson KAJ, Whelan L, Zhu J, Dockery A, Wynne NC, Cairns RM, Kirk C, Turner J, Duignan ES, O'Byrne JJ, Silvestri G, Kenna PF, Farrar GJ, Keegan DJ. Stephenson KAJ, et al. Among authors: silvestri g. Invest Ophthalmol Vis Sci. 2023 Jul 3;64(10):23. doi: 10.1167/iovs.64.10.23. Invest Ophthalmol Vis Sci. 2023. PMID: 37466950 Free PMC article.
Characterization of West African Crystalline Macular Dystrophy in the Ghanaian Population.
Amoaku WM, Sampalli A, Silvestri V, Cushley LN, Akafo S, Amissah-Arthur KN, Lartey S, Hageman CN, Hubbard WC, Pappas CM, Zouache MA, Stevenson M, Hageman GS, Silvestri G; Ghana AMD Study Group. Amoaku WM, et al. Among authors: silvestri g. Ophthalmol Retina. 2022 Aug;6(8):723-731. doi: 10.1016/j.oret.2022.03.006. Epub 2022 Mar 18. Ophthalmol Retina. 2022. PMID: 35307605
Target 5000: a standardized all-Ireland pathway for the diagnosis and management of inherited retinal degenerations.
Stephenson KAJ, Zhu J, Wynne N, Dockery A, Cairns RM, Duignan E, Whelan L, Malone CP, Dempsey H, Collins K, Routledge S, Pandey R, Crossan E, Turner J, O'Byrne JJ, Brady L, Silvestri G, Kenna PF, Farrar GJ, Keegan DJ. Stephenson KAJ, et al. Among authors: silvestri g. Orphanet J Rare Dis. 2021 May 5;16(1):200. doi: 10.1186/s13023-021-01841-1. Orphanet J Rare Dis. 2021. PMID: 33952326 Free PMC article.
72 results