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ARVO Annual Meeting Abstract July 2019

A novel mutation in PEX1 gene causes an Usher-like Syndrome with early onset of Retinitis Pigmentosa and Sensorineural Hearing Loss

Maria Rosaria Barillari; Raffaella Brunetti-Pierri; Valentina Di lorio; Antonella De Benedictis; Anna Nesti; Paolo Melillo; Nicola Angelillo; Gerarda Cappuccio; Nicola Brunetti-Pierri; Umberto Barillari; Sandro Banfi; Francesco Testa; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4492. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Chromatic Pupillometry for Screening and Monitoring of Retinitis Pigmentosa

Paolo Melillo; Antonella De Benedictis; Edoardo Villani; Maria Concetta Ferraro; Ernesto Iadanza; Monica Gherardelli; Francesco Testa; Sandro Banfi; Paolo Nucci; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4513. doi: https://doi.org/

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. doi: https://doi.org/

ARVO Annual Meeting Abstract September 2016

Clinical phenotype and progression of Usher syndrome related to mutations in MYO7A or USH2A

Francesco Testa; Raffaella Colucci; Antonella De Benedictis; Vincenzo Marcelli; Elio Marciano; Alberto Auricchio; Anne Kurtenbach; Christine Petit; Crystel Bonnet; Eberhart Zrenner; Francesca Simonelli

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):151. doi: https://doi.org/

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. doi: https://doi.org/

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