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Year | Number of Results |
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Page 1
Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa.
Ophthalmology. 2019 Nov;126(11):1549-1556. doi: 10.1016/j.ophtha.2019.04.038. Epub 2019 May 1.
Ophthalmology. 2019.
PMID: 31054281
Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease.
Gao FJ, Wang DD, Chen F, Sun HX, Hu FY, Xu P, Li J, Liu W, Qi YH, Li W, Wang M, Zhang S, Xu GZ, Chang Q, Wu JH.
Gao FJ, et al.
Br J Ophthalmol. 2021 Jan;105(1):87-92. doi: 10.1136/bjophthalmol-2020-315878. Epub 2020 Mar 18.
Br J Ophthalmol. 2021.
PMID: 32188678
Free PMC article.
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Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.
Zein WM, Falsini B, Tsilou ET, Turriff AE, Schultz JM, Friedman TB, Brewer CC, Zalewski CK, King KA, Muskett JA, Rehman AU, Morell RJ, Griffith AJ, Sieving PA.
Zein WM, et al.
Invest Ophthalmol Vis Sci. 2014 Nov 25;56(1):107-14. doi: 10.1167/iovs.14-15355.
Invest Ophthalmol Vis Sci. 2014.
PMID: 25425308
Free PMC article.
Clinical Trial.
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Comparison of 5-year progression of retinitis pigmentosa involving the posterior pole among siblings by means of SD-OCT: a retrospective study.
Colombo L, Montesano G, Sala B, Patelli F, Maltese P, Abeshi A, Bertelli M, Rossetti L.
Colombo L, et al.
BMC Ophthalmol. 2018 Jun 26;18(1):153. doi: 10.1186/s12886-018-0817-z.
BMC Ophthalmol. 2018.
PMID: 29940899
Free PMC article.
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Spectral-Domain Optical Coherence Tomography Analysis in Syndromic and Nonsyndromic Forms of Retinitis Pigmentosa due to USH2A Genetic Variants.
Colombo L, Maltese PE, Romano D, Fogagnolo P, Castori M, Marceddu G, Cristofoli F, Percio M, Piteková B, Modarelli AM, Bertelli M, Rossetti L.
Colombo L, et al.
Ophthalmic Res. 2022;65(2):180-195. doi: 10.1159/000520329. Epub 2021 Nov 15.
Ophthalmic Res. 2022.
PMID: 34781295
Free article.
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