Clinical characteristics and current therapies for inherited retinal degenerations
Sahel, José-Alain, Marazova, Katia, Audo, Isabelle
Published in Cold Spring Harbor perspectives in medicine (01.02.2015)
Published in Cold Spring Harbor perspectives in medicine (01.02.2015)
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First identification of ITM2B interactome in the human retina
Wohlschlegel, J., Argentini, M., Michiels, C., Letellier, C., Forster, V., Condroyer, C., He, Z., Thuret, G., Zeitz, C., Léger, T., Audo, I.
Published in Scientific reports (26.08.2021)
Published in Scientific reports (26.08.2021)
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CRISPR/Cas9: From research to therapeutic application
Ben Yacoub, T, Wohlschlegel, J, Sahel, J-A, Zeitz, C, Audo, I
Published in Journal francais d'ophtalmologie (01.04.2023)
Published in Journal francais d'ophtalmologie (01.04.2023)
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Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness
Neuillé, M., Malaichamy, S., Vadalà, M., Michiels, C., Condroyer, C., Sachidanandam, R., Srilekha, S., Arokiasamy, T., Letexier, M., Démontant, V., Sahel, J.-A., Sen, P., Audo, I., Soumittra, N., Zeitz, C.
Published in Clinical epigenetics (01.06.2016)
Published in Clinical epigenetics (01.06.2016)
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A novel nonsense variant in REEP6 is involved in a sporadic rod‐cone dystrophy case
Méjécase, C., Mohand‐Saïd, S., El Shamieh, S., Antonio, A., Condroyer, C., Blanchard, S., Letexier, M., Saraiva, J.‐P., Sahel, J.‐A., Audo, I., Zeitz, C.
Published in Clinical genetics (01.03.2018)
Published in Clinical genetics (01.03.2018)
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Variability of chloroquine and hydroxychloroquine retinopathy among various ethnicities
Giocanti-Aurégan, A, Couturier, A, Girmens, J-F, Le Mer, Y, Massamba, N, Barreau, E, Audo, I
Published in Journal francais d'ophtalmologie (01.04.2018)
Published in Journal francais d'ophtalmologie (01.04.2018)
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Journal Article
Retinal degeneration in mucopolysaccharidose type II
Liang, F., Audo, I., Sahel, J. A., Paques, M.
Published in Graefe's archive for clinical and experimental ophthalmology (01.07.2013)
Published in Graefe's archive for clinical and experimental ophthalmology (01.07.2013)
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ARL2BP mutations account for 0.1% of autosomal recessive rod‐cone dystrophies with the report of a novel splice variant
Audo, I., El Shamieh, S., Méjécase, C., Michiels, C., Demontant, V., Antonio, A., Condroyer, C., Boyard, F., Letexier, M., Saraiva, J.‐P., Blanchard, S., Mohand‐Saïd, S., Sahel, J.‐A., Zeitz, C.
Published in Clinical genetics (01.07.2017)
Published in Clinical genetics (01.07.2017)
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Multimodal imaging and functional correlations identify unusual cases of macular retinal pigment epithelium hypopigmentation occurring without functional loss
Boulanger-Scemama, E., Akesbi, J., Tick, S., Mohand-Said, S., Sahel, J.-A., Audo, I.
Published in Documenta ophthalmologica (01.08.2017)
Published in Documenta ophthalmologica (01.08.2017)
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Update on recommendations for screening for hydroxychloroquine retinopathy
Couturier, A, Giocanti-Aurégan, A, Dupas, B, Girmens, J-F, Le Mer, Y, Massamba, N, Barreau, E, Audo, I
Published in Journal francais d'ophtalmologie (01.11.2017)
Published in Journal francais d'ophtalmologie (01.11.2017)
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Journal Article
Progressive retinal dysfunction in diffuse unilateral subacute neuroretinitis
Audo, I, Webster, A R, Bird, A C, Holder, G E, Kidd, M N
Published in British journal of ophthalmology (01.06.2006)
Published in British journal of ophthalmology (01.06.2006)
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Three‐Year Safety Results of SAR422459 (EIAV‐ABCA4) Gene Therapy in Patients With ABCA4‐Associated Stargardt Disease: An Open‐Label Dose‐Escalation Phase I/IIa Clinical Trial, Cohorts 1‐5
Parker, Maria A., Erker, Laura R., Audo, Isabelle, Choi, Dongseok, Mohand-Said, Saddek, Sestakauskas, Kastytis, Benoit, Patrick, Appelqvist, Terence, Krahmer, Melissa, Ségaut-Prévost, Caroline, Lujan, Brandon J., Faridi, Ambar, Chegarnov, Elvira N., Steinkamp, Peter N., Ku, Cristy, da Palma, Mariana Matioli, Barale, Pierre-Olivier, Ayelo-Scheer, Sarah, Lauer, Andreas, Stout, Tim, Wilson, David J., Weleber, Richard G., Pennesi, Mark E., Sahel, José Alain, Yang, Paul
Published in American journal of ophthalmology (01.08.2022)
Published in American journal of ophthalmology (01.08.2022)
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PRO131 WHAT DO WE KNOW ABOUT PATIENT'S AND CAREGIVERS' EXPERIENCE WHEN LIVING WITH THE HEREDITARY RETINAL CONDITION RETINITIS PIGMENTOSA?
Banhazi, J., Williamson, N., Bradley, H., Exall, E., Naujoks, C., Spera, C., Green, J., Fischer, M.D., Audo, I., Kay, C., Viriato, D.
Published in Value in health (01.11.2019)
Published in Value in health (01.11.2019)
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Journal Article
CRISPR/Cas9 : de la recherche à l’application thérapeutique
Ben Yacoub, T., Wohlschlegel, J., Sahel, J.-A., Zeitz, C., Audo, I.
Published in Journal français d'ophtalmologie (01.04.2023)
Published in Journal français d'ophtalmologie (01.04.2023)
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