Passerini I - Search Results

1

Myopic Macular Hole and Detachment after Gene Therapy in Atypical RPE65 Retinal Dystrophy: A Case Report.

Giansanti F, Nicolosi C, Giorgio D, Sodi A, Mucciolo DP, Pavese L, Pollazzi L, Virgili G, Vicini G, Passerini I, Pelo E, Murro V. Giansanti F, et al. Among authors: passerini i. Genes (Basel). 2024 Jul 4;15(7):879. doi: 10.3390/genes15070879. Genes (Basel). 2024. PMID: 39062658 Free PMC article.

2

Long-Term Results of Photodynamic Therapy for Choroidal Neovascularization in Pediatric Patients with Best Vitelliform Macular Dystrophy.

Sodi A, Murro V, Caporossi O, Passerini I, Bacci GM, Caputo R, Menchini U. Sodi A, et al. Among authors: passerini i. Ophthalmic Genet. 2015 Jun;36(2):168-74. doi: 10.3109/13816810.2015.1009121. Epub 2015 Feb 12. Ophthalmic Genet. 2015. PMID: 25675349

3

Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers.

Murro V, Mucciolo DP, Passerini I, Palchetti S, Sodi A, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Graefes Arch Clin Exp Ophthalmol. 2017 Nov;255(11):2099-2111. doi: 10.1007/s00417-017-3751-5. Epub 2017 Jul 27. Graefes Arch Clin Exp Ophthalmol. 2017. PMID: 28752371

4

Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy.

Murro V, Mucciolo DP, Sodi A, Passerini I, Giorgio D, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Graefes Arch Clin Exp Ophthalmol. 2019 Jan;257(1):9-22. doi: 10.1007/s00417-018-4161-z. Epub 2018 Oct 15. Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 30324420

5

Multimodal imaging of benign yellow dot maculopathy.

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Pacini B, Finocchio L, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Ophthalmic Genet. 2019 Apr;40(2):135-140. doi: 10.1080/13816810.2019.1589529. Epub 2019 Apr 3. Ophthalmic Genet. 2019. PMID: 30942106

6

Optical Coherence Tomography Angiography (OCT-A) in young choroideremia (CHM) patients.

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Ophthalmic Genet. 2019 Jun;40(3):201-206. doi: 10.1080/13816810.2019.1611880. Epub 2019 May 28. Ophthalmic Genet. 2019. PMID: 31135252

7

Peculiar Clinical Findings in Young Choroideremia Patients: A Retrospective Case Review.

Mucciolo DP, Murro V, Sodi A, Passerini I, Giorgio D, Virgili G, Rizzo S. Mucciolo DP, et al. Among authors: passerini i. Ophthalmologica. 2019;242(4):195-207. doi: 10.1159/000501282. Epub 2019 Aug 15. Ophthalmologica. 2019. PMID: 31416074

8

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. Among authors: passerini i. Ophthalmic Genet. 2019 Oct;40(5):421-427. doi: 10.1080/13816810.2019.1666881. Epub 2019 Sep 21. Ophthalmic Genet. 2019. PMID: 31544579

9

Optical coherence tomography (OCT) features of cystoid spaces in choroideremia (CHM).

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Bacci G, Bargiacchi S, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Graefes Arch Clin Exp Ophthalmol. 2019 Dec;257(12):2655-2663. doi: 10.1007/s00417-019-04508-7. Epub 2019 Oct 26. Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 31654189

10

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

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