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Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.
Karali M, Testa F, Di Iorio V, Torella A, Zeuli R, Scarpato M, Romano F, Onore ME, Pizzo M, Melillo P, Brunetti-Pierri R, Passerini I, Pelo E, Cremers FPM, Esposito G, Nigro V, Simonelli F, Banfi S. Karali M, et al. Among authors: passerini i. Sci Rep. 2022 Dec 2;12(1):20815. doi: 10.1038/s41598-022-24636-1. Sci Rep. 2022. PMID: 36460718 Free PMC article.
A novel GRK1 mutation in an Italian patient with Oguchi disease.
Mucciolo DP, Sodi A, Murro V, Passerini I, Palchetti S, Pelo E, Virgili G, Rizzo S. Mucciolo DP, et al. Among authors: passerini i. Ophthalmic Genet. 2018 Jan-Feb;39(1):137-138. doi: 10.1080/13816810.2017.1323341. Epub 2017 May 16. Ophthalmic Genet. 2018. PMID: 28511019 No abstract available.
Fundus phenotype in retinitis pigmentosa associated with EYS mutations.
Mucciolo DP, Sodi A, Passerini I, Murro V, Cipollini F, Borg I, Pelo E, Contini E, Virgili G, Rizzo S. Mucciolo DP, et al. Among authors: passerini i. Ophthalmic Genet. 2018 Oct;39(5):589-602. doi: 10.1080/13816810.2018.1509351. Epub 2018 Aug 28. Ophthalmic Genet. 2018. PMID: 30153090
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease.
Sodi A, Passerini I, Bacherini D, Boni L, Palchetti S, Murro V, Caporossi O, Mucciolo DP, Franco F, Vannozzi L, Torricelli F, Pelo E, Rizzo S, Virgili G. Sodi A, et al. Among authors: passerini i. Ophthalmic Genet. 2018 Dec;39(6):699-705. doi: 10.1080/13816810.2018.1525753. Epub 2018 Oct 4. Ophthalmic Genet. 2018. PMID: 30285522
En face OCT in choroideremia.
Murro V, Mucciolo DP, Sodi A, Giorgio D, Passerini I, Pelo E, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Ophthalmic Genet. 2019 Dec;40(6):514-520. doi: 10.1080/13816810.2019.1711429. Epub 2020 Jan 13. Ophthalmic Genet. 2019. PMID: 31928275
58 results