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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. doi:

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. doi:

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. doi: https://doi.org/10.1167/iovs.61.14.36

Includes: Supplemental Content

Retina December 2019

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

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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. doi: https://doi.org/10.1167/iovs.19-27100

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2017

CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy

Cécile Méjécase; Saddek Mohand-Said; Camille Andrieux; Aurélie Hummel; Saïd El Shamieh; Aline Antonio; Fiona Boyard; Christel Condroyer; Christelle Michiels; Steven Blanchard; Mélanie Letexier; Jean-Paul Saraiva; Jose Alain Sahel; Christina Zeitz; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):573. doi:

ARVO Annual Meeting Abstract June 2017

Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches

Christina Zeitz; Christelle Michiels; Marion Neuille; Christoph Friedburg; Christel Condroyer; Fiona Boyard; Aline Antonio; Markus N Preising; Vincent Meyer; Anne Boland; Jean-François Deleuze; Lilia Mesrob; Bernhard Jurklies; Birgit Lorenz; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):575. doi:

ARVO Annual Meeting Abstract June 2017

Mutation spectrum of a French cohort with autosomal recessive bestrophynopathy

Isabelle S Audo; Saddek Mohand-Said; Brigitte Ekpe; Aline Antonio; Christel Condroyer; Fiona Boyard; José Alain sahel; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1239. doi:

ARVO Annual Meeting Abstract September 2016

MERTK mutations account for 2% of cases with inherited retinal dystrophy in a large French cohort

Isabelle S Audo; Elise Boulanger-Semama; Saddek Mohand-Said; Vanessa Démontant; Christel Condroyer; Aline Antonio; Fiona Boyard; Said El Shamieh; Jose Sahel; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):660. doi:

ARVO Annual Meeting Abstract September 2016

How multimodal retinal imaging can help with Next Generation Sequencing interpretation: the example of cone and cone-rod dystrophies

Elise Boulanger-Semama; Said El Shamieh; Saddek Mohand-Said; Vanessa Démontant; Christel Condroyer; Aline Antonio; Christelle Michiels; Fiona Boyard; Jose Sahel; Christina Zeitz; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3169. doi:

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