Search | IOVS | ARVO Journals

Access Provided By:
MIT Libraries

Forgot password?

Create an Account

View

Showing 1 – 7 of 7

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract June 2024

Dysfunction of vitamin A metabolism and phospholipid transport contribute to dominant and recessive RDH12 -retinopathies

Cécile Méjécase; Nicholas Owen; Pablo Soro Barrio; Riccardo Cheloni; Neelima Nair; Hajrah Sarkar; Lyes Toualbi; Mariya Moosajee

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):1580.

ARVO Annual Meeting Abstract June 2024

Identification of a novel gene defect UBAP1L underlying for autosomal recessive rod-cone and cone-rod dystrophy

Isabelle S Audo; julien Navarro; Leila Azizzadeh; Cécile Méjécase; Shahad Albadri; Andrea Amprou; Tasnim Ben Yacoub; Juliette Wohlschlegel; Lorenzo Bianco; Alessio ANTROPOLI; Marco Nassisi; Said El Shameh; Vasily M. Smirnov; Jose Sahel; Filippo Del Bene; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):1518.

ARVO Annual Meeting Abstract June 2023

Characterisation of induced pluripotent stem cell derived retinal organoid models of RDH12 -retinopathies

Cécile Méjécase; Nicholas Owen; Hajrah Sarkar; Lyes Toualbi; Mariya Moosajee

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):3194.

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.

ARVO Annual Meeting Abstract July 2019

A CCDC51 frameshift variant as a candidate gene defect for autosomal recessive rod-cone dystrophy

Christina Zeitz; Cécile Méjécase; Saddek Mohand-Saïd; Lisa Emmengger; Audrey Schalk; Marion Neuillé; Elise Orhan; Frédéric Blond; Camille Prévot; Sandra Sandra Chantot-Bastaraud; Thierry D Leveillard; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):415.

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.

Advertisement