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Retina June 2024

Multicentric Longitudinal Prospective Study in a European Cohort of MYO7A Patients: Disease Course and Implications for Gene Therapy

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Francesco Testa; Ester Carreño; L. Ingeborgh van den Born; Paolo Melillo; Irene Perea-Romero; Valentina Di Iorio; Giulia Risca; Clemente Maria Iodice; Ronald J. E. Pennings; Marianthi Karali; Sandro Banfi; Alberto Auricchio; Stefania Galimberti; Carmen Ayuso; Francesca Simonelli
TAGS: cohort studies, disease progression, european continental ancestry group, gene therapy, prospective studies, usher syndrome, eye
Invest. Ophthalmol. Vis. Sci.. 2024; 65(6):25. https://doi.org/10.1167/iovs.65.6.25

Includes: Supplemental Content

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 2024

Multicentric longitudinal prospective study in Usher Syndrome due to MYO7A mutations: disease course and implications for gene therapy

Clemente Maria Iodice; Ester Carreño; L. Ingeborgh van den Born; Paolo Melillo; Irene Perea-Romero; Valentina Di Iorio; Giulia Risca; Ronald J.E. Pennings; Marianthi Karali; Sandro Banfi; Alberto Auricchio; Stefania Galimberti; Francesco Testa; Carmen Ayuso; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):2136.

ARVO Annual Meeting Abstract June 2024

Cystoid Macular Edema in Patients with Retinitis Pigmentosa and its Genetic Association

Danila Pisani; Marianthi Karali; Valentina Di Iorio; Lorenzo Cantile; Emanuele Madonna; Antonio Niccolò; Raffaella Colucci; Antonella De Benedictis; Paolo Melillo; Francesco Testa; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3116.

ARVO Annual Meeting Abstract June 2024

Early Onset Macular Drusen associated to rare variants in CFH-gene

Luciana Damiano; Marianthi Karali; Clemente Maria Iodice; Danila Pisani; Valentina Di Iorio; Anna Nesti; Paolo Melillo; Francesco Testa; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):4436.

ARVO Annual Meeting Abstract June 2023

Anatomic and functional retinal changes in female carriers of pathogenic variants in RPGR gene

Valentina Di Iorio; Luciana Damiano; Raffaella Colucci; Antonio Del Giudice; Carlo Gesualdo; Paolo Melillo; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4666.

ARVO Annual Meeting Abstract June 2023

Clinical findings in Retinitis Pigmentosa related to CNGB1 variants

Andrea Attilio Rosolia; Valentina Di Iorio; Marianthi Karali; Anna Nesti; Paolo Melillo; Francesco Testa; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4665.

ARVO Annual Meeting Abstract June 2023

Longitudinal natural history study of dominant retinitis pigmentosa due to RHO gene mutations

Clemente Maria Iodice; Valentina Di Iorio; Antonella De Benedictis; Gabriella Esposito; Marianthi Karali; Paolo Melillo; Francesco Testa; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4652.

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.

ARVO Annual Meeting Abstract June 2023

Curcuma Longa and Boswellia Serrata Oral Administration in patients with Treatment-Naïve Diabetic Macular Edema

CLAUDIO IOVINO; Valentina Di Iorio; Andrea Attilio Rosolia; Irene Schiavetti; Michele Lanza; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):2686.

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

Retina July 2021

Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal Study

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Francesco Testa; Andrea Sodi; Sabrina Signorini; Valentina Di Iorio; Vittoria Murro; Raffaella Brunetti-Pierri; Enza Maria Valente; Marianthi Karali; Paolo Melillo; Sandro Banfi; Francesca Simonelli
TAGS: cohort studies, genes, longitudinal studies, mutation, phenotype, severity of illness, pathologic nystagmus, introns, genotype, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2021; 62(9):1. https://doi.org/10.1167/iovs.62.9.1

Retina December 2020

Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations

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Valentina Di Iorio; Marianthi Karali; Paolo Melillo; Francesco Testa; Raffaella Brunetti-Pierri; Francesco Musacchia; Christel Condroyer; John Neidhardt; Isabelle Audo; Christina Zeitz; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2020; 61(14):36. https://doi.org/10.1167/iovs.61.14.36

Includes: Supplemental Content

Articles May 2020

Biofeedback Rehabilitation and Visual Cortex Response in Stargardt's Disease: A Randomized Controlled Trial

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Paolo Melillo; Anna Prinster; Valentina Di Iorio; Gaia Olivo; Francesco Maria D'Alterio; Sirio Cocozza; Mario Quarantelli; Francesco Testa; Arturo Brunetti; Francesca Simonelli
TAGS: biofeedback (psychology), functional magnetic resonance imaging, randomized controlled trial, rehabilitation, stargardt's disease, visual cortex, vision, reading (activity), eye
Trans. Vis. Sci. Tech.. 2020; 9(6):6. https://doi.org/10.1167/tvst.9.6.6

Retina April 2019

CHM/REP1 Transcript Expression and Loss of Visual Function in Patients Affected by Choroideremia

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Valentina Di Iorio; Gabriella Esposito; Francesca De Falco; Rosa Boccia; Tiziana Fioretti; Raffaella Colucci; Giuseppe De Rosa; Paolo Melillo; Francesco Salvatore; Francesca Simonelli; Francesco Testa
TAGS: choroideremia, genotype, phenotype, vision
Invest. Ophthalmol. Vis. Sci.. 2019; 60(5):1547-1555. https://doi.org/10.1167/iovs.18-25501

Visual Neuroscience March 2018

Visual Cortex Activation in Patients With Stargardt Disease

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Paolo Melillo; Anna Prinster; Valentina Di Iorio; Gaia Olivo; Francesco Maria D'Alterio; Sirio Cocozza; Ada Orrico; Mario Quarantelli; Francesco Testa; Arturo Brunetti; Francesca Simonelli
TAGS: electroretinography, functional magnetic resonance imaging, stargardt's disease, visual cortex, primary visual cortex, eye
Invest. Ophthalmol. Vis. Sci.. 2018; 59(3):1503-1511. https://doi.org/10.1167/iovs.17-22900

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

A new syndromic form of retinal degeneration due to mutations in the PCYT1A gene

Mariaelena Filippelli; Rosa Boccia; Raffaella Colucci; Valentina Di Iorio; Anna Nesti; Maria Rosaria Barillari; Nicola Brunetti Pierri; Francesco Testa; Sandro Banfi; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):128.

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

Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial.

Francesco Maria D'Alterio; Paolo Melillo; Valentina Di Iorio; Gaia Olivo; Anna Prinster; Arturo Brunetti; Mario Quarantelli; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2688.

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Multicentric Longitudinal Prospective Study in a European Cohort of MYO7A Patients: Disease Course and Implications for Gene Therapy

Chorioretinal atrophy after treatment with Voretigene Neparvovec in clinical practice

Multicentric longitudinal prospective study in Usher Syndrome due to MYO7A mutations: disease course and implications for gene therapy

Cystoid Macular Edema in Patients with Retinitis Pigmentosa and its Genetic Association

Early Onset Macular Drusen associated to rare variants in CFH-gene

Anatomic and functional retinal changes in female carriers of pathogenic variants in RPGR gene

Clinical findings in Retinitis Pigmentosa related to CNGB1 variants

Longitudinal natural history study of dominant retinitis pigmentosa due to RHO gene mutations

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

Curcuma Longa and Boswellia Serrata Oral Administration in patients with Treatment-Naïve Diabetic Macular Edema

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

Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal Study

Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations

Biofeedback Rehabilitation and Visual Cortex Response in Stargardt's Disease: A Randomized Controlled Trial

CHM/REP1 Transcript Expression and Loss of Visual Function in Patients Affected by Choroideremia

Visual Cortex Activation in Patients With Stargardt Disease

A new syndromic form of retinal degeneration due to mutations in the PCYT1A gene

Clinical presentation and disease course in Choroideremia patients

Clinical and genetic study of late onset Stargardt disease

Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial.

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