Management of albinism: French guidelines for diagnosis and care von Moreno‐Artero, E., Morice‐Picard, F., Bremond‐Gignac, D., Drumare‐Bouvet, I., Duncombe‐Poulet, C., Leclerc‐Mercier, S., Dufresne, H., Kaplan, J., Jouanne, B., Arveiler, B., Taieb, A., Hadj‐Rabia, S.

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Optic disc drusen in children: Advantages of various imaging modalities von Naoum, S, Bouacha, I, Drumare, I, Marks, C, Defoort-Delemmes, S

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The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands von Rocatcher, Aude, Desquiret-Dumas, Valérie, Charif, Majida, Ferré, Marc, Gohier, Philippe, Mirebeau-Prunier, Delphine, Verny, Christophe, Milea, Dan, Lenaers, Guy, Bonneau, Dominique, Reynier, Pascal, Amati-Bonneau, Patrizia

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Senior-Løken syndrome: About two cases von Grunewald, O., Fajardy, I., Drumare, I., Defoort-Dhellemmes, S., Dhaenens, C.

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Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness von Vincent, Ajoy, Audo, Isabelle, Tavares, Erika, Maynes, Jason T., Tumber, Anupreet, Wright, Thomas, Li, Shuning, Michiels, Christelle, Banin, Eyal, Bocquet, Beatrice, De Baere, Elfride, Casteels, Ingele, Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Friedburg, Christoph, Gottlob, Irene, Jacobson, Samuel G., Kellner, Ulrich, Koenekoop, Robert, Kohl, Susanne, Leroy, Bart P., Lorenz, Birgit, McLean, Rebecca, Meire, Francoise, Meunier, Isabelle, Munier, Francis, de Ravel, Thomy, Reiff, Charlotte M., Mohand-Saïd, Saddek, Sharon, Dror, Schorderet, Daniel, Schwartz, Sharon, Zanlonghi, Xavier, Condroyer, Christel, MacDonald, Heather, Verdet, Robert, Sahel, José-Alain, Hamel, Christian P., Zeitz, Christina, Héon, Elise

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Aicardi syndrome with unilateral ocular involvement von Tabary, A, Vangheluwe, V, Defoort-Dhellemmes, S, Drumare-Bouvet, I

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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, I, Kohl, S, Leroy, B P, Munier, F L, Guillonneau, X, Mohand-Saïd, S, Bujakowska, K, Nandrot, E F, Lorenz, B, Preising, M, Kellner, U, Renner, A B, Bernd, A, Antonio, A, Moskova-Doumanova, V, Lancelot, M E, Poloschek, C M, Drumare, I, Defoort-Dhellemmes, S, Wissinger, B, Léveillard, T, Hamel, C P, Schorderet, D F, De Baere, E, Berger, W, Jacobson, S G, Zrenner, E, Sahel, J A, Bhattacharya, S S, Zeitz, C

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Malformation artérioveineuse rétinienne dans le cadre du syndrome de Bonnet-Dechaume-Blanc von Blin, J., Marks, C., Drumare, I., Smirnov, V.

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Congenital achromatopsia: electroretinogram in early diagnosis von Defoort-Dhellemmes, S, Lebrun, T, Arndt, C F, Bouvet-Drumare, I, Guilbert, F, Puech, B, Hache, J-C

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Atteintes ophtalmologiques unilatérales dans le syndrome d’Aicardi von Tabary, A., Vangheluwe, V., Defoort-Dhellemmes, S., Drumare-Bouvet, I.

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Dietary, environmental, and genetic risk factors of Extensive Macular Atrophy with Pseudodrusen, a severe bilateral macular atrophy of middle-aged patients von Douillard, A, Picot, MC, Delcourt, C, Defoort-Dhellemmes, S, Marzouka, NAD, Lacroux, A, Zanlonghi, X, Drumare, I, Jozefowicz, E, Bocquet, B, Baudoin, C, Perez-Roustit, S, Arsène, S, Gissot, V, Devin, F, Arndt, C, Wolff, B, Mauget-Faÿsse, M, Quaranta, M, Mura, T, Deplanque, D, Oubraham, H, Cohen, SY, Gastaud, P, Zambrowski, O, Creuzot-Garcher, C, Saïd, SM, Sahel, JA, Souied, E, Milazzo, S, Garavito, RB, Kalatzis, V, Puech, B, Hamel, C, Audo, I, Meunier, I

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Druses de la papille de l’enfant : intérêt des différents examens d’imagerie von Naoum, S., Bouacha, I., Drumare, I., Marks, C., Defoort-Delemmes, S.

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A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 gene von Meunier, I, Bocquet, B, Labesse, G, Zeitz, C, Defoort-Dhellemmes, S, Lacroux, A, Mauget-Faysse, M, Drumare, I, Gamez, A-S, Mathieu, C, Marquette, V, Sagot, L, Dhaenens, C-M, Arndt, C, Carroll, P, Remy-Jardin, M, Cohen, SY, Sahel, J-A, Puech, B, Audo, I, Mrejen, S, Hamel, CP

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Improvement of downbeat nystagmus after suboccipital decompression for Chiari I malformation von Denion, Eric, Defoort-Dhellemmes, Sabine, Arndt, Carl-Friedrich, Bouvet-Drumare, Isabelle, Beaussart, Karine, Hache, Jean-Claude, Dhellemmes, Patrick

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Simplified electroretinography protocol and diagnosis of retinal dystrophies in children von Dhellemmes, S D, Vincent, F, Arndt, C, Drumare, I B, Hache, J C

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Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy von Charif, M, Chevrollier, A, Gueguen, N, Bris, C, Goudenège, D, Desquiret-Dumas, V, Leruez, S, Colin, E, Meunier, A, Vignal, C, Smirnov, V, Defoort-Dhellemmes, S, Drumare Bouvet, I, Goizet, C, Votruba, M, Jurkute, N, Yu-Wai-Man, P, Tagliavini, F, Caporali, L, La Morgia, C, Carelli, V, Procaccio, V, Zanlonghi, X, Meunier, I, Reynier, P, Bonneau, D, Amati-Bonneau, P, Lenaers, G

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Achromatopsie congénitale : intérêt de l’électrorétinogramme pour le diagnostic précoce von Defoort-Dhellemmes, S., Lebrun, T., Arndt, C.F., Bouvet-Drumare, I., Guilbert, F., Puech, B., Hache, J.-C.

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Protocole simplifié d'électrorétinographie et diagnostic des dystrophies rétiniennes de l'enfant von DEFOORT DHELLEMMES, S, VINCENT, F, ARNDT, C, BOUVET DRUMARE, I, HACHE, J.-C

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118 Intérêt de l’enquête génétique pour les nystagmus congénitaux von Drumare Bouvet, I., Defoort-Dhellemmes, S.

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Peanut allergens are rapidly transferred in human breast milk and can prevent sensitization in mice von Bernard, H, Ah-Leung, S, Drumare, M-F, Feraudet-Tarisse, C, Verhasselt, V, Wal, J-M, Créminon, C, Adel-Patient, K

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