Cases von Audo, I.

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Clinical characteristics and current therapies for inherited retinal degenerations von Sahel, José-Alain, Marazova, Katia, Audo, Isabelle

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Cases von Audo, I.

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First identification of ITM2B interactome in the human retina von Wohlschlegel, J., Argentini, M., Michiels, C., Letellier, C., Forster, V., Condroyer, C., He, Z., Thuret, G., Zeitz, C., Léger, T., Audo, I.

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Of fluid and tubes von Nassisi, M., Sahel, J.-A., Audo, I.

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CRISPR/Cas9: from research to therapeutic application von Ben Yacoub, T, Wohlschlegel, J, Sahel, J-A, Zeitz, Christina, Audo, I

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Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness von 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.

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A novel nonsense variant in REEP6 is involved in a sporadic rod‐cone dystrophy case von 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.

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Variability of chloroquine and hydroxychloroquine retinopathy among various ethnicities von Giocanti-Aurégan, A, Couturier, A, Girmens, J-F, Le Mer, Y, Massamba, N, Barreau, E, Audo, I

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ARL2BP mutations account for 0.1% of autosomal recessive rod‐cone dystrophies with the report of a novel splice variant von 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.

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Retinal degeneration in mucopolysaccharidose type II von Liang, F., Audo, I., Sahel, J. A., Paques, M.

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Multimodal imaging and functional correlations identify unusual cases of macular retinal pigment epithelium hypopigmentation occurring without functional loss von Boulanger-Scemama, E., Akesbi, J., Tick, S., Mohand-Said, S., Sahel, J.-A., Audo, I.

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Update on recommendations for screening for hydroxychloroquine retinopathy von Couturier, A, Giocanti-Aurégan, A, Dupas, B, Girmens, J-F, Le Mer, Y, Massamba, N, Barreau, E, Audo, I

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Cases von AUDO, I

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Progressive retinal dysfunction in diffuse unilateral subacute neuroretinitis von Audo, I, Webster, A R, Bird, A C, Holder, G E, Kidd, M N

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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, Coho... von 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

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The Negative ERG: Clinical Phenotypes and Disease Mechanisms of Inner Retinal Dysfunction von Audo, Isabelle, MD, PhD, Robson, Anthony G., PhD, Holder, Graham E., PhD, Moore, Anthony T., MA, FRCS, FRCOphth, F MedSci

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Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium von Thompson, Debra A, Ali, Robin R, Banin, Eyal, Branham, Kari E, Flannery, John G, Gamm, David M, Hauswirth, William W, Heckenlively, John R, Iannaccone, Alessandro, Jayasundera, K Thiran, Khan, Naheed W, Molday, Robert S, Pennesi, Mark E, Reh, Thomas A, Weleber, Richard G, Zacks, David N

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PRO131 WHAT DO WE KNOW ABOUT PATIENT'S AND CAREGIVERS' EXPERIENCE WHEN LIVING WITH THE HEREDITARY RETINAL CONDITION RETINITIS PIGMENTOSA? von Banhazi, J., Williamson, N., Bradley, H., Exall, E., Naujoks, C., Spera, C., Green, J., Fischer, M.D., Audo, I., Kay, C., Viriato, D.

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Retinal and cochlear toxicity of drugs: new insights into mechanisms and detection von Audo, Isabelle, Warchol, Mark E

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