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ARVO Annual Meeting Abstract June 2024

Chorioretinal atrophy after treatment with Voretigene Neparvovec in clinical practice

Michele Della Corte; Paolo Melillo; Clemente Maria Iodice; Valentina Di Iorio; Danila Pisani; Amelia Citro; Settimio Rossi; Marianthi Karali; Francesco Testa; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):910.

ARVO Annual Meeting Abstract June 2023

Chromatic pupillometry as an objective outcome to evaluate effects of Voretigene Neparvovec treatment in patients with RPE65 -related inherited retinal dystrophies

Francesco Testa; Paolo Melillo; Valentina Di Iorio; Amelia Citro; Settimio Rossi; MIchele Della Corte; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5445.

Special Issue September 2021

Voretigene Neparvovec Gene Therapy in Clinical Practice: Treatment of the First Two Italian Pediatric Patients

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Francesco Testa; Paolo Melillo; Michele Della Corte; Valentina Di Iorio; Raffaella Brunetti-Pierri; Amelia Citro; Maurizio Ferrara; Marianthi Karali; Rosa Annibale; Sandro Banfi; Settimio Rossi; Francesca Simonelli

Trans. Vis. Sci. Tech.. 2021; 10(10):11. https://doi.org/10.1167/tvst.10.10.11

ARVO Annual Meeting Abstract June 2017

Correlation between visual cortex activation and macular parameters in patients with Stargardt disease.

Francesco Maria D'Alterio; Paolo Melillo; Michele Della Corte; Gaia Olivo; Sirio Cocozza; Anna Prinster; Arturo Brunetti; Mario Quarantelli; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4645.

ARVO Annual Meeting Abstract June 2017

A natural history study to explore genotype / phenotype correlations in Stargardt disease

Valentina Di lorio; Ada Orrico; Paolo Melillo; Francesco Testa; Michele Della Corte; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4646.

ARVO Annual Meeting Abstract June 2017

The effects of oral carbonic anhydrase inhibitors in patients affected by X-linked Retinoschisis

Francesco Testa; Beatrice Gallo; Mario Marchese; Valentina Di lorio; Anna Nesti; Michele Della Corte; Paolo Melillo; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4643.

ARVO Annual Meeting Abstract September 2016

Clinical presentation and disease course in Choroideremia patients

Raffaella Colucci; Rosa Boccia; Valentina Di Iorio; Ada Orrico; Paolo Melillo; Settimio Rossi; Michele Della Corte; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):159.

ARVO Annual Meeting Abstract September 2016

Clinical and genetic study of late onset Stargardt disease

Ada Orrico; Paolo Melillo; Valentina Di Iorio; Settimio Rossi; Michele Della Corte; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2684.

ARVO Annual Meeting Abstract September 2016

Comparison of en-face Optical Coherence Tomography and Fundus Autofluorescence for assessment of macular lesion area in Stargardt disease

Paolo Melillo; Ada Orrico; Valentina Di Iorio; Anna Nesti; Settimio Rossi; Michele Della Corte; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2690.

ARVO Annual Meeting Abstract September 2016

Functional and morphological assessment of patients with idiopatic epiretinal membrane after surgical treatment

Giancarlo Dell'Aversana Orabona; Beatrice Gallo; Ada Orrico; Paolo Melillo; Settimio Rossi; Francesco Testa; Michele Della Corte; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4067.

ARVO Annual Meeting Abstract September 2016

Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome

Beatrice Gallo; Raffaella Colucci; Antonella De Benedictis; Raffaella Brunetti-Pierri; Paolo Melillo; Settimio Rossi; Francesco Testa; Claudio Azzolini; Michele Della Corte; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4071.

ARVO Annual Meeting Abstract June 2013

Rule of multifocal electroretinogram in follow-up of ABCA4-related Stardgardt’s disease

Ada Orrico; Francesco Testa; Settimio Rossi; Paolo Melillo; Antonella de Benedictis; Michele Della Corte; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1371.

ARVO Annual Meeting Abstract June 2013

Macular function in patients with macular pucker treated with 23 gauge vitrectomy

Giancarlo Dell'Aversana Orabona; Angelo Rampone; Luigi Di Perna; Francesco Testa; Settimio Rossi; Michele Della Corte; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3337.

Retina July 2012

Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy

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Francesco Testa; Settimio Rossi; Andrea Sodi; Ilaria Passerini; Valentina Di Iorio; Michele Della Corte; Sandro Banfi; Enrico Maria Surace; Ugo Menchini; Alberto Auricchio; Francesca Simonelli
TAGS: electroretinography, gene therapy, personal integrity, photoreceptors, stargardt's disease, vision, fundus autofluorescence imaging, mutation
Invest. Ophthalmol. Vis. Sci.. 2012; 53(8):4409-4415. https://doi.org/10.1167/iovs.11-8201

Retina July 2011

Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy

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Francesco Testa; Enrico Maria Surace; Settimio Rossi; Elena Marrocco; Annagiusi Gargiulo; Valentina Di Iorio; Carmela Ziviello; Anna Nesti; Simona Fecarotta; Maria Laura Bacci; Massimo Giunti; Michele della Corte; Sandro Banfi; Alberto Auricchio; Francesca Simonelli
TAGS: gene therapy, italian, leber's amaurosis, mice, mutation, spatial vectors, suidae, retina, photoreceptors
Invest. Ophthalmol. Vis. Sci.. 2011; 52(8):5618-5624. https://doi.org/10.1167/iovs.10-6543

ARVO Annual Meeting Abstract April 2011

Macular Morphological and Functional Evaluation in Italian Patients with Stargardt Disease

Michele Della Corte; Settimio Rossi; Francesco Testa; Andrea Sodi; Enrico Maria Surace; Ilaria Passerini; Valentina Di Iorio; Ugo Menchini; Alberto Auricchio; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5016.

ARVO Annual Meeting Abstract April 2011

Characterization of Italian Bietti Crystalline Dystrophy Patients with CYP4V2 Mutations

Settimio Rossi; Francesco Testa; Michele Della Corte; Anren Li; Valentina Di Iorio; Carlo Gesualdo; J. Fielding Hejtmancik; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):1833.

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Chorioretinal atrophy after treatment with Voretigene Neparvovec in clinical practice

Chromatic pupillometry as an objective outcome to evaluate effects of Voretigene Neparvovec treatment in patients with RPE65 -related inherited retinal dystrophies

Voretigene Neparvovec Gene Therapy in Clinical Practice: Treatment of the First Two Italian Pediatric Patients

Correlation between visual cortex activation and macular parameters in patients with Stargardt disease.

A natural history study to explore genotype / phenotype correlations in Stargardt disease

The effects of oral carbonic anhydrase inhibitors in patients affected by X-linked Retinoschisis

Clinical presentation and disease course in Choroideremia patients

Clinical and genetic study of late onset Stargardt disease

Comparison of en-face Optical Coherence Tomography and Fundus Autofluorescence for assessment of macular lesion area in Stargardt disease

Functional and morphological assessment of patients with idiopatic epiretinal membrane after surgical treatment

Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome

Rule of multifocal electroretinogram in follow-up of ABCA4-related Stardgardt’s disease

Macular function in patients with macular pucker treated with 23 gauge vitrectomy

Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy

Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy

Macular Morphological and Functional Evaluation in Italian Patients with Stargardt Disease

Characterization of Italian Bietti Crystalline Dystrophy Patients with CYP4V2 Mutations

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