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

Year Number of Results
1996 2
1997 1
1998 2
2000 1
2001 1
2002 1
2003 5
2004 3
2005 4
2006 6
2007 8
2008 14
2009 6
2010 8
2011 12
2012 15
2013 10
2014 11
2015 10
2016 8
2017 12
2018 13
2019 16
2020 18
2021 19
2022 15
2023 12
2024 9

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202 results

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Page 1
Phase 1 clinical study of an embryonic stem cell-derived retinal pigment epithelium patch in age-related macular degeneration.
da Cruz L, Fynes K, Georgiadis O, Kerby J, Luo YH, Ahmado A, Vernon A, Daniels JT, Nommiste B, Hasan SM, Gooljar SB, Carr AF, Vugler A, Ramsden CM, Bictash M, Fenster M, Steer J, Harbinson T, Wilbrey A, Tufail A, Feng G, Whitlock M, Robson AG, Holder GE, Sagoo MS, Loudon PT, Whiting P, Coffey PJ. da Cruz L, et al. Among authors: robson ag. Nat Biotechnol. 2018 Apr;36(4):328-337. doi: 10.1038/nbt.4114. Epub 2018 Mar 19. Nat Biotechnol. 2018. PMID: 29553577 Free article. Clinical Trial.
Electrophysiology in neuro-ophthalmology.
Jurkute N, Robson AG. Jurkute N, et al. Among authors: robson ag. Handb Clin Neurol. 2021;178:79-96. doi: 10.1016/B978-0-12-821377-3.00019-2. Handb Clin Neurol. 2021. PMID: 33832688
Unilateral BEST1-Associated Retinopathy.
Arora R, Khan K, Kasilian ML, Strauss RW, Holder GE, Robson AG, Thompson DA, Moore AT, Michaelides M. Arora R, et al. Among authors: robson ag. Am J Ophthalmol. 2016 Sep;169:24-32. doi: 10.1016/j.ajo.2016.05.024. Epub 2016 Jun 7. Am J Ophthalmol. 2016. PMID: 27287821 Free PMC article.
CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History.
Daich Varela M, Georgiou M, Alswaiti Y, Kabbani J, Fujinami K, Fujinami-Yokokawa Y, Khoda S, Mahroo OA, Robson AG, Webster AR, AlTalbishi A, Michaelides M. Daich Varela M, et al. Among authors: robson ag. Am J Ophthalmol. 2023 Feb;246:107-121. doi: 10.1016/j.ajo.2022.09.002. Epub 2022 Sep 12. Am J Ophthalmol. 2023. PMID: 36099972 Free PMC article.
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes.
Georgiou M, Robson AG, Fujinami K, de Guimarães TAC, Fujinami-Yokokawa Y, Daich Varela M, Pontikos N, Kalitzeos A, Mahroo OA, Webster AR, Michaelides M. Georgiou M, et al. Among authors: robson ag. Prog Retin Eye Res. 2024 Jan 24;100:101244. doi: 10.1016/j.preteyeres.2024.101244. Online ahead of print. Prog Retin Eye Res. 2024. PMID: 38278208 Review.
KCNV2-associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3.
de Guimaraes TAC, Georgiou M, Robson AG, Fujinami K, Vincent A, Nasser F, Khateb S, Mahroo OA, Pontikos N, Vargas ME, Thiadens AAHJ, Carvalho ER, Nguyen XT, Arno G, Fujinami-Yokokawa Y, Liu X, Tsunoda K, Hayashi T, Jiménez-Rolando B, Martin-Merida MI, Avila-Fernandez A, Salas EC, Garcia-Sandoval B, Ayuso C, Sharon D, Kohl S, Huckfeldt RM, Banin E, Pennesi ME, Khan AO, Wissinger B, Webster AR, Heon E, Boon CJF, Zrenner E, Michaelides M. de Guimaraes TAC, et al. Among authors: robson ag. Br J Ophthalmol. 2023 Oct 18:bjo-2023-323640. doi: 10.1136/bjo-2023-323640. Online ahead of print. Br J Ophthalmol. 2023. PMID: 37852740 Free article.
202 results