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ARVO Annual Meeting Abstract June 2024

Six-year results of a Phase I/IIa gene therapy trial in patients with Usher Syndrome Type-1B (USH1B)

Maria Parker; Paul Yang; Dongseok Choi; Saddek Mohand-Said; Shobana Aravind; Ambar Faridi; Elvira Chegarnov; Charles Butler; Pierre-Olivier Barale; Andreas K Lauer; Tim Stout; David Wilson; Richard Weleber; Mark E Pennesi; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5327.

ARVO Annual Meeting Abstract June 2023

Visual search with natural scenes: validation of a new virtual reality outcome in inherited retinal disease.

Caroline Kurek; Alireza Talebi; Alexis Defer; Saddek Mohand-Said; Philippe Chaumet-Riffaud; Isabelle S Audo; Jose Sahel; Colas Nils Authié

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5526.

ARVO Annual Meeting Abstract June 2023

Development of a real-life mobility test for the performance evaluation of advanced retinitis pigmentosa subjects

Chloé Pagot; Mylène Poujade; Karine Becker; Suzon Ajasse; Cécilia Coen; Caroline De Montleau; Magali Taiel; Saddek Mohand-Said; Jose Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5041.

ARVO Annual Meeting Abstract June 2022

A prospective, multicentre, randomised, double-blind study designed to assess the potential effects of omega-3 fatty acids supplementation in dry age-related macular degeneration or Stargardt disease

Katerina Prokopiou; Panagiotis Kolovos; Haritini Tsangari; Francesco Bandello; Luca M Rossetti; Leonardo Mastropasqua; Saddek Mohand-Said; Tassos Georgiou

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):377 – F0208.

ARVO Annual Meeting Abstract June 2022

Genotype-phenotype correlation and disease modeling in RPGR -related cone and cone-rod dystrophies.

Marco Nassisi; Giuseppe De Bartolo; Saddek Mohand-Said; Christel Condroyer; Aline Antonio; Marie-Elise Lancelot; Kinga Maria Bujakowska; Vasily M. SMIRNOV; Thomas Pugliese; John Neidhardt; Jose Alain Sahel; Christina Zeitz; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):138 – A0318.

ARVO Annual Meeting Abstract June 2022

Development and validation of a mobility test for Inherited Retinal Disease in real and virtual conditions - preliminary results.

Colas Nils Authié; Mylène Poujade; Alireza Talebi; Alexis Defer; Ariel Zenouda; Cecilia Coen; Yihan Zhang; Jose Alain Sahel; Saddek Mohand-Said; Philippe Chaumet-Riffaud; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):715 – F0443.

ARVO Annual Meeting Abstract June 2022

Retrospective natural history of retinitis pigmentosa due to RHO , PDE6A, or PDE6B mutations: the PHENOROD1 study

Alice Le Meur; Daniel C Chung; Léa Thiebault; Pierre-Axel Vinot; Berthe Pom; Thierry D Leveillard; Saddek Mohand-Said; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4497 – F0284.

ARVO Annual Meeting Abstract June 2022

Prospective natural history of retinitis pigmentosa due to RHO , PDE6A , or PDE6B mutations: interim analysis of the PHENOROD2 study

Anne Celle; Alice Le Meur; Daniel C Chung; Saddek Mohand-Said; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4294.

ARVO Annual Meeting Abstract June 2022

The impact of luminance and disease stage on navigation performance in age related macular degeneration (AMD) - a MACUSTAR study report

Ariel Zenouda; Alina Schenk; Amina Abdirahman; Charlotte Behning; José-Alain Sahel; Adnan Tufail; Nadia Zakaria; Nick Tyler; Saddek Mohand-Said; Michel Paques; Ulrich F O Luhmann; Hannah M P Dunbar

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2456 – F0033.

Genetics April 2022

Retinal Phenotype of Patients with CLRN1 -Associated Usher 3A Syndrome in French Light4Deaf Cohort

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Vasily M. Smirnov; Marco Nassisi; Saddek Mohand-Saïd; Crystel Bonnet; Anne Aubois; Céline Devisme; Thilissa Dib; Christina Zeitz; Natalie Loundon; Sandrine Marlin; Christine Petit; Bahram Bodaghi; José-Alain Sahel; Isabelle Audo
TAGS: cohort studies, french, phenotype, syndrome
Invest. Ophthalmol. Vis. Sci.. 2022; 63(4):25. https://doi.org/10.1167/iovs.63.4.25

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2021

Retinal degeneration in abetalipoproteinemia

Vasily M. SMIRNOV; Fanny Mochel; Saddek Mohand-Said; Camille Andrieu; Christel Condroyer; Jose Alain Sahel; Christina Zeitz; Isabelle Audo

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3216.

ARVO Annual Meeting Abstract June 2021

Simultaneous Perception of Prosthetic and Natural Vision in Patients with Geographic Atrophy

Daniel V Palanker; Yannick Le Mer; Ralf Hornig; Guillaume Buc; Saddek Mohand-Said; Jose Alain Sahel

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3556.

ARVO Annual Meeting Abstract June 2021

Correlations between progression markers in rod-cone dystrophy due to mutations in RHO, PDE6A, or PDE6B .

Daniel C Chung; Pierre-Axel VINOT; Myriam Marussig; Léa Thiébault; Berthe Pom; Camille Andrieu; Christina Zeitz; Thierry D Leveillard; Stephane Boissel; Saddek Mohand-Said; Isabelle Audo; Jose-Alain Sahel

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3539.

ARVO Annual Meeting Abstract June 2021

PHENOTYPE-GENOTYPE CORRELATION AND PROGRESSION MODELING APPLIED TO MUTATIONS IN RPGR -RELATED ROD-CONE DYSTROPHY.

Marco Nassisi; Giuseppe De Bartolo; Saddek Mohand-Said; Vasily M. SMIRNOV; Aline Antonio; Christel Condroyer; Jose Alain Sahel; Christina Zeitz; Isabelle Audo

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3238.

ARVO Annual Meeting Abstract June 2020

Natural history of retinitis pigmentosa due to RHO , PDE6A OR PDE6B mutations

Myriam Marussig; Léa Thiebault; Pierre-Axel Vinot; Berthe Pom; Camille Andrieu; Christina Zeitz; Thierry D Leveillard; Florence Allouche; Saddek Mohand-Said; Isabelle S Audo; Jose Alain Sahel

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3035.

ARVO Annual Meeting Abstract June 2020

PRESENTATION AND LONG-TERM CLINICAL COURSE OF ITM2B-RELATED RETINAL DYSTROPHY

Marco Nassisi; Juliette Wohlschlegel; Saddek Mohand-Said; Christophe Habas; Jose Alain Sahel; Christina Zeitz; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3194.

ARVO Annual Meeting Abstract June 2020

Photovoltaic Restoration of Sight in Atrophic Age-Related Macular Degeneration: one-year follow-up

Daniel V Palanker; Yannick Le Mer; Saddek Mohand-Said; Ralf Hornig; Guillaume Buc; Martin Deterre; Jose Alain Sahel

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):4302.

ARVO Annual Meeting Abstract June 2020

Retinal degeneration in CLRN1 -associated Usher type 3A syndrome.

Vasily M. SMIRNOV; Saddek Mohand-Saïd; Chrystel Bonnet; Céline Devisme; Camille Andrieu; Christina Zeitz; Sandrine Marlin; Christine Petit; Bahram Bodaghi; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3033.

Retina December 2019

Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease

PDF

Marco Nassisi; Saddek Mohand-Saïd; Camille Andrieu; Aline Antonio; Christel Condroyer; Cécile Méjécase; Claire-Marie Dhaenens; José-Alain Sahel; Christina Zeitz; Isabelle Audo
TAGS: autofluorescence, stargardt's disease, electroretinography, body tissue
Invest. Ophthalmol. Vis. Sci.. 2019; 60(15):4951-4957. https://doi.org/10.1167/iovs.19-27100

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Mutations in WDR34 is a rare cause of non-syndromic autosomal recessive rod-cone dystrophy

Isabelle S Audo; Maria Solaguren-Beascoa; Kinga Bujakowska; Cécile Méjécase; Lisa Emmengger; Saddek Mohand-Said; Thierry D Leveillard; Eric A Pierce; Helene Dollfus; Jose Alain Sahel; Shomi Bhattacharya; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):381.

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Six-year results of a Phase I/IIa gene therapy trial in patients with Usher Syndrome Type-1B (USH1B)

Visual search with natural scenes: validation of a new virtual reality outcome in inherited retinal disease.

Development of a real-life mobility test for the performance evaluation of advanced retinitis pigmentosa subjects

A prospective, multicentre, randomised, double-blind study designed to assess the potential effects of omega-3 fatty acids supplementation in dry age-related macular degeneration or Stargardt disease

Genotype-phenotype correlation and disease modeling in RPGR -related cone and cone-rod dystrophies.

Development and validation of a mobility test for Inherited Retinal Disease in real and virtual conditions - preliminary results.

Retrospective natural history of retinitis pigmentosa due to RHO , PDE6A, or PDE6B mutations: the PHENOROD1 study

Prospective natural history of retinitis pigmentosa due to RHO , PDE6A , or PDE6B mutations: interim analysis of the PHENOROD2 study

The impact of luminance and disease stage on navigation performance in age related macular degeneration (AMD) - a MACUSTAR study report

Retinal Phenotype of Patients with CLRN1 -Associated Usher 3A Syndrome in French Light4Deaf Cohort

Retinal degeneration in abetalipoproteinemia

Simultaneous Perception of Prosthetic and Natural Vision in Patients with Geographic Atrophy

Correlations between progression markers in rod-cone dystrophy due to mutations in RHO, PDE6A, or PDE6B .

PHENOTYPE-GENOTYPE CORRELATION AND PROGRESSION MODELING APPLIED TO MUTATIONS IN RPGR -RELATED ROD-CONE DYSTROPHY.

Natural history of retinitis pigmentosa due to RHO , PDE6A OR PDE6B mutations

PRESENTATION AND LONG-TERM CLINICAL COURSE OF ITM2B-RELATED RETINAL DYSTROPHY

Photovoltaic Restoration of Sight in Atrophic Age-Related Macular Degeneration: one-year follow-up

Retinal degeneration in CLRN1 -associated Usher type 3A syndrome.

Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease

Mutations in WDR34 is a rare cause of non-syndromic autosomal recessive rod-cone dystrophy

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