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Page 1
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. Ophthalmic Genet. 2018 Oct;39(5):589-602. doi: 10.1080/13816810.2018.1509351. Epub 2018 Aug 28. Ophthalmic Genet. 2018. PMID: 30153090
En face OCT in Stargardt disease.
Sodi A, Mucciolo DP, Cipollini F, Murro V, Caporossi O, Virgili G, Rizzo S. Sodi A, et al. Among authors: mucciolo dp. Graefes Arch Clin Exp Ophthalmol. 2016 Sep;254(9):1669-79. doi: 10.1007/s00417-015-3254-1. Epub 2016 Jan 7. Graefes Arch Clin Exp Ophthalmol. 2016. PMID: 26743751
Retinal capillaritis in a CRB1-associated retinal dystrophy.
Murro V, Mucciolo DP, Sodi A, Vannozzi L, De Libero C, Simonini G, Rizzo S. Murro V, et al. Among authors: mucciolo dp. Ophthalmic Genet. 2017 Dec;38(6):555-558. doi: 10.1080/13816810.2017.1281966. Epub 2017 Jan 27. Ophthalmic Genet. 2017. PMID: 28129017
Reading Ability and Quality of Life in Stargardt Disease.
Murro V, Sodi A, Giacomelli G, Mucciolo DP, Pennino M, Virgili G, Rizzo S. Murro V, et al. Among authors: mucciolo dp. Eur J Ophthalmol. 2017 Nov 8;27(6):740-745. doi: 10.5301/ejo.5000972. Eur J Ophthalmol. 2017. PMID: 28430335
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. 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.
55 results