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Page 1
Extended optical treatment versus early patching with an intensive patching regimen in children with amblyopia in Europe (EuPatch): a multicentre, randomised controlled trial.
Proudlock FA, Hisaund M, Maconachie G, Papageorgiou E, Manouchehrinia A, Dahlmann-Noor A, Khandelwal P, Self J, Beisse C, Gottlob I; EUPatch study group. Proudlock FA, et al. Among authors: maconachie g. Lancet. 2024 May 4;403(10438):1766-1778. doi: 10.1016/S0140-6736(23)02893-3. Lancet. 2024. PMID: 38704172 Free article. Clinical Trial.
Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.
Lee YR, Thomas MG, Roychaudhury A, Skinner C, Maconachie G, Crosier M, Horak H, Constantinescu CS, Choi TI, Kyung JJ, Wang T, Ku B, Chodirker BN, Hammer MF, Gottlob I, Norton WHJ, Chudley AE, Schwartz CE, Kim CH. Lee YR, et al. Among authors: maconachie g. Res Sq [Preprint]. 2023 Mar 20:rs.3.rs-2683050. doi: 10.21203/rs.3.rs-2683050/v1. Res Sq. 2023. PMID: 36993381 Free PMC article. Preprint.
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Kuht HJ, Maconachie GDE, Han J, Kessel L, van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, Jiao Y, Smirnov V, Choi JH, Tobin MD, Sheth V, Purohit R, Dawar B, Girach A, Strul S, May L, Chen FK, Heath Jeffery RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arveiler B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, Thomas MG. Kuht HJ, et al. Among authors: maconachie gde. Ophthalmology. 2022 Jun;129(6):708-718. doi: 10.1016/j.ophtha.2022.02.010. Epub 2022 Feb 11. Ophthalmology. 2022. PMID: 35157951 Free PMC article.
Albinism Associated With Torsional Nystagmus Masquerading as Spasmus Nutans.
Kuht HJ, McLean RJ, Aamir A, Maconachie GDE, Gottlob I, Thomas MG. Kuht HJ, et al. Among authors: maconachie gde. J Neuroophthalmol. 2023 Dec 1;43(4):e313-e315. doi: 10.1097/WNO.0000000000001417. Epub 2021 Dec 16. J Neuroophthalmol. 2023. PMID: 34924531 No abstract available.
Ocular Manifestations of PNPT1-Related Neuropathy.
Kuht HJ, Thomas KA, Hisaund M, Maconachie GDE, Thomas MG. Kuht HJ, et al. Among authors: maconachie gde. J Neuroophthalmol. 2021 Sep 1;41(3):e293-e296. doi: 10.1097/WNO.0000000000001012. J Neuroophthalmol. 2021. PMID: 34415280 No abstract available.
Clinical utility gene card for FRMD7-related infantile nystagmus.
Dawar B, Kuht HJ, Han J, Maconachie GDE, Thomas MG. Dawar B, et al. Among authors: maconachie gde. Eur J Hum Genet. 2021 Oct;29(10):1584-1588. doi: 10.1038/s41431-021-00826-9. Epub 2021 Feb 25. Eur J Hum Genet. 2021. PMID: 33633368 Free PMC article. No abstract available.
Discordant phenotypes in twins with infantile nystagmus.
Aamir A, Kuht HJ, McLean RJ, Maconachie GDE, Sheth V, Dawar B, Purohit R, Sylvius N, Hisaund M, Zubcov-Iwantscheff A, Proudlock FA, Gottlob I, Thomas MG. Aamir A, et al. Among authors: maconachie gde. Sci Rep. 2021 Feb 2;11(1):2826. doi: 10.1038/s41598-021-82368-0. Sci Rep. 2021. PMID: 33531592 Free PMC article.
Current and emerging treatments for albinism.
Liu S, Kuht HJ, Moon EH, Maconachie GDE, Thomas MG. Liu S, et al. Among authors: maconachie gde. Surv Ophthalmol. 2021 Mar-Apr;66(2):362-377. doi: 10.1016/j.survophthal.2020.10.007. Epub 2020 Oct 29. Surv Ophthalmol. 2021. PMID: 33129801 Review.
33 results