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Page 1
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study.
Igelman AD, White E, Tayyib A, Everett L, Vincent A, Heon E, Zeitz C, Michaelides M, Mahroo OA, Katta M, Webster A, Preising M, Lorenz B, Khateb S, Banin E, Sharon D, Luski S, Van Den Broeck F, Leroy BP, De Baere E, Walraedt S, Stingl K, Kuehlewein L, Kohl S, Reith M, Fulton A, Raghuram A, Meunier I, Dollfus H, Aleman TS, Bedoukian EC, O'Neil EC, Krauss E, Vincent A, Jordan C, Iannaccone A, Sen P, Sundaramurthy S, Nagasamy S, Balikova I, Casteels I, Borooah S, Yassin S, Nagiel A, Schwartz H, Zanlonghi X, Gottlob I, McLean RJ, Munier FL, Stephenson A, Sisk R, Koenekoop R, Wilson LB, Fredrick D, Choi D, Yang P, Pennesi ME. Igelman AD, et al. Among authors: fulton a. Br J Ophthalmol. 2024 Jul 30:bjo-2023-323747. doi: 10.1136/bjo-2023-323747. Online ahead of print. Br J Ophthalmol. 2024. PMID: 39079892
Evaluating the Utility of Initial Exams in Retinopathy of Prematurity: Proposal of FIRST-ROP Algorithm for a Medium-Risk Cohort.
Altamirano F, Yuan M, Hoyek S, Hu D, Abidi M, Chaaya C, De Bruyn H, Fulton A, Mantagos IS, Wu C, Gise R, Gonzalez E, VanderVeen DK, Patel NA. Altamirano F, et al. Among authors: fulton a. Ophthalmology. 2025 Jan 8:S0161-6420(25)00005-3. doi: 10.1016/j.ophtha.2025.01.004. Online ahead of print. Ophthalmology. 2025. PMID: 39793656
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Refractive errors in patients with Bardet Biedl syndrome.
Yavuz Saricay L, Baldwin G, Moulton EA, Gonzalez E, Rajabi F, Hunter DG, Fulton AB. Yavuz Saricay L, et al. Among authors: fulton ab. Ophthalmic Genet. 2024 Oct;45(5):435-440. doi: 10.1080/13816810.2024.2357296. Epub 2024 Jul 2. Ophthalmic Genet. 2024. PMID: 38953718
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. 2024 May 1;18(3):396-399. doi: 10.1097/ICB.0000000000001397. Retin Cases Brief Rep. 2024. PMID: 36729003
585 results