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Year Number of Results
2016 3
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2018 10
2019 13
2020 12
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2022 4
2023 2
2024 1

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53 results

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Page 1
Choroidal Caverns in Stargardt Disease.
Mucciolo DP, Giorgio D, Lippera M, Dattilo V, Passerini I, Pelo E, Sodi A, Virgili G, Giansanti F, Murro V. Mucciolo DP, et al. Invest Ophthalmol Vis Sci. 2022 Feb 1;63(2):25. doi: 10.1167/iovs.63.2.25. Invest Ophthalmol Vis Sci. 2022. PMID: 35156991 Free PMC article.
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice.
Murro V, Banfi S, Testa F, Iarossi G, Falsini B, Sodi A, Signorini S, Iolascon A, Russo R, Mucciolo DP, Caputo R, Bacci GM, Bargiacchi S, Turco S, Fortini S, Simonelli F. Murro V, et al. Among authors: mucciolo dp. Orphanet J Rare Dis. 2023 Jul 31;18(1):223. doi: 10.1186/s13023-023-02798-z. Orphanet J Rare Dis. 2023. PMID: 37525225 Free PMC article. Review.
Optic nerve involvement in CACNA1F-related disease: observations from a multicentric case series.
Marziali E, Van Den Broeck F, Bargiacchi S, Fortunato P, Caputo R, Sodi A, De Zaeytijd J, Murro V, Mucciolo DP, Giorgio D, Passerini I, Palazzo V, Peluso F, de Baere E, Zeitz C, Leroy BP, Secci J, Bacci GM. Marziali E, et al. Among authors: mucciolo dp. Ophthalmic Genet. 2023 Apr;44(2):152-162. doi: 10.1080/13816810.2022.2132514. Epub 2022 Dec 5. Ophthalmic Genet. 2023. PMID: 36469668
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: mucciolo dp. Ophthalmic Genet. 2019 Dec;40(6):514-520. doi: 10.1080/13816810.2019.1711429. Epub 2020 Jan 13. Ophthalmic Genet. 2019. PMID: 31928275
CHOROIDAL VASCULARITY INDEX IN YOUNG CHOROIDEREMIA PATIENTS.
Murro V, Mucciolo DP, Giorgio D, Passerini I, Cipollini F, Virgili G, Giansanti F, Sodi A. Murro V, et al. Among authors: mucciolo dp. Retina. 2021 May 1;41(5):1018-1025. doi: 10.1097/IAE.0000000000002960. Retina. 2021. PMID: 32826791
Near-infrared autofluorescence in young choroideremia patients.
Mucciolo DP, Murro V, Giorgio D, Sodi A, Passerini I, Virgili G, Rizzo S. Mucciolo DP, et al. Ophthalmic Genet. 2019 Oct;40(5):421-427. doi: 10.1080/13816810.2019.1666881. Epub 2019 Sep 21. Ophthalmic Genet. 2019. PMID: 31544579
Long-term follow-up of a CRB1-associated maculopathy.
Mucciolo DP, Murro V, Giorgio D, Passerini I, Sodi A, Virgili G, Rizzo S. Mucciolo DP, et al. Ophthalmic Genet. 2018 Aug;39(4):522-525. doi: 10.1080/13816810.2018.1479431. Epub 2018 Jun 5. Ophthalmic Genet. 2018. PMID: 29869924
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
Clinical and molecular findings in patients with pattern dystrophy.
Sodi A, Mucciolo DP, Giorgio D, Passerini I, Pacini B, Bruschi M, Verdina T, Virgili G, Giansanti F, Murro V. Sodi A, et al. Among authors: mucciolo dp. Ophthalmic Genet. 2021 Oct;42(5):577-587. doi: 10.1080/13816810.2021.1938140. Epub 2021 Jul 9. Ophthalmic Genet. 2021. PMID: 34240658
53 results