Di Iorio V - Search Results

1

Newman H, Perlman I, Pras E, Rozenberg A, Ben-Yosef T, Iovino C, Simonelli F, Di Iorio V, Rotenstreich Y, Katzburg E, Ehrenberg M, Iglicki M, Zur D. Newman H, et al. Among authors: di iorio v. Retina. 2022 Oct 1;42(10):e49. doi: 10.1097/IAE.0000000000003564. Retina. 2022. PMID: 36129272 No abstract available.

2

The role of optical coherence tomography in an atypical case of oculocutaneous albinism: a case report.

Rossi S, Testa F, Gargiulo A, Di Iorio V, Pierri RB, D'Alterio FM, Corte MD, Surace E, Simonelli F. Rossi S, et al. Among authors: di iorio v. Case Rep Ophthalmol. 2012 Jan;3(1):113-7. doi: 10.1159/000337489. Epub 2012 Mar 27. Case Rep Ophthalmol. 2012. PMID: 22548044 Free PMC article.

3

Macular abnormalities in Italian patients with retinitis pigmentosa.

Testa F, Rossi S, Colucci R, Gallo B, Di Iorio V, della Corte M, Azzolini C, Melillo P, Simonelli F. Testa F, et al. Among authors: di iorio v. Br J Ophthalmol. 2014 Jul;98(7):946-50. doi: 10.1136/bjophthalmol-2013-304082. Epub 2014 Feb 13. Br J Ophthalmol. 2014. PMID: 24532797 Free PMC article.

4

Macular function and morphologic features in juvenile stargardt disease: longitudinal study.

Testa F, Melillo P, Di Iorio V, Orrico A, Attanasio M, Rossi S, Simonelli F. Testa F, et al. Among authors: di iorio v. Ophthalmology. 2014 Dec;121(12):2399-405. doi: 10.1016/j.ophtha.2014.06.032. Epub 2014 Aug 2. Ophthalmology. 2014. PMID: 25097154 Free PMC article.

5

En Face Spectral-Domain Optical Coherence Tomography for the Monitoring of Lesion Area Progression in Stargardt Disease.

Melillo P, Testa F, Rossi S, Di Iorio V, Orrico A, Auricchio A, Simonelli F. Melillo P, et al. Among authors: di iorio v. Invest Ophthalmol Vis Sci. 2016 Jul 1;57(9):OCT247-52. doi: 10.1167/iovs.15-18751. Invest Ophthalmol Vis Sci. 2016. PMID: 27409479 Free PMC article.

6

Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy.

Testa F, Filippelli M, Brunetti-Pierri R, Di Fruscio G, Di Iorio V, Pizzo M, Torella A, Barillari MR, Nigro V, Brunetti-Pierri N, Simonelli F, Banfi S. Testa F, et al. Among authors: di iorio v, di fruscio g. Eur J Hum Genet. 2017 May;25(5):651-655. doi: 10.1038/ejhg.2017.23. Epub 2017 Mar 8. Eur J Hum Genet. 2017. PMID: 28272537 Free PMC article.

7

Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies.

Di Iorio V, Karali M, Brunetti-Pierri R, Filippelli M, Di Fruscio G, Pizzo M, Mutarelli M, Nigro V, Testa F, Banfi S, Simonelli F. Di Iorio V, et al. Among authors: di fruscio g. Genes (Basel). 2017 Oct 20;8(10):280. doi: 10.3390/genes8100280. Genes (Basel). 2017. PMID: 29053603 Free PMC article.

8

The renal lesions in Bardet-Biedl Syndrome: history before and after the discovery of BBS genes.

Viggiano D, Zacchia M, Simonelli F, Di Iorio V, Anastasio P, Capasso G, De Santo NG. Viggiano D, et al. Among authors: di iorio v. G Ital Nefrol. 2018 Feb;35(Suppl 70):95-100. G Ital Nefrol. 2018. PMID: 29482283 Free article. No abstract available.

9

Visual Cortex Activation in Patients With Stargardt Disease.

Melillo P, Prinster A, Di Iorio V, Olivo G, D'Alterio FM, Cocozza S, Orrico A, Quarantelli M, Testa F, Brunetti A, Simonelli F. Melillo P, et al. Among authors: di iorio v. Invest Ophthalmol Vis Sci. 2018 Mar 1;59(3):1503-1511. doi: 10.1167/iovs.17-22900. Invest Ophthalmol Vis Sci. 2018. PMID: 29625472

10

ASSOCIATION BETWEEN GENOTYPE AND DISEASE PROGRESSION IN ITALIAN STARGARDT PATIENTS: A Retrospective Natural History Study.

Di Iorio V, Orrico A, Esposito G, Melillo P, Rossi S, Sbordone S, Auricchio A, Testa F, Simonelli F. Di Iorio V, et al. Retina. 2019 Jul;39(7):1399-1409. doi: 10.1097/IAE.0000000000002151. Retina. 2019. PMID: 29642238

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