Central Crosstalk for Somatic Tinnitus: Abnormal Vergence Eye Movements

Por Yang, Qing, Vernet, Marine, Orssaud, Christophe, Bonfils, Pierre, Londero, Alain, Kapoula, Zoi
Publicado em 2010

Differential auditory-oculomotor interactions in patients with right vs. left sided subjective tinnitus: a saccade study

Por Lang, Alexandre, Vernet, Marine, Yang, Qing, Orssaud, Christophe, Londero, Alain, Kapoula, Zoï
Publicado em 2013

Saccade-vergence properties remain more stable over short-time repetition under overlap than under gap task: a preliminary study

Por Lang, Alexandre, Gaertner, Chrystal, Ghassemi, Elham, Yang, Qing, Orssaud, Christophe, Kapoula, Zoï
Publicado em 2014

Objective Evaluation of Vergence Disorders and a Research-Based Novel Method for Vergence Rehabilitation

Por Kapoula, Zoï, Morize, Aurélien, Daniel, François, Jonqua, Fabienne, Orssaud, Christophe, Brémond-Gignac, Dominique
Publicado no Transl Vis Sci Technol (2016)

Benefit of Bi-Ocular Visual Stimulation for Postural Control in Children with Strabismus

Por Gaertner, Chrystal, Creux, Charlotte, Espinasse-Berrod, Marie-Andrée, Orssaud, Christophe, Dufier, Jean-Louis, Kapoula, Zoï
Publicado em 2013

Medio-Lateral Postural Instability in Subjects with Tinnitus

Por Kapoula, Zoi, Yang, Qing, Lê, Thanh-Thuan, Vernet, Marine, Berbey, Nolwenn, Orssaud, Christophe, Londero, Alain, Bonfils, Pierre
Publicado em 2011

Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy

Por Achilli, Alessandro, Iommarini, Luisa, Olivieri, Anna, Pala, Maria, Hooshiar Kashani, Baharak, Reynier, Pascal, La Morgia, Chiara, Valentino, Maria Lucia, Liguori, Rocco, Pizza, Fabio, Barboni, Piero, Sadun, Federico, De Negri, Anna Maria, Zeviani, Massimo, Dollfus, Helene, Moulignier, Antoine, Ducos, Ghislaine, Orssaud, Christophe, Bonneau, Dominique, Procaccio, Vincent, Leo-Kottler, Beate, Fauser, Sascha, Wissinger, Bernd, Amati-Bonneau, Patrizia, Torroni, Antonio, Carelli, Valerio
Publicado em 2012

Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations

Por Perrault, Isabelle, Saunier, Sophie, Hanein, Sylvain, Filhol, Emilie, Bizet, Albane A., Collins, Felicity, Salih, Mustafa A.M., Gerber, Sylvie, Delphin, Nathalie, Bigot, Karine, Orssaud, Christophe, Silva, Eduardo, Baudouin, Véronique, Oud, Machteld M., Shannon, Nora, Le Merrer, Martine, Roche, Olivier, Pietrement, Christine, Goumid, Jamal, Baumann, Clarisse, Bole-Feysot, Christine, Nitschke, Patrick, Zahrate, Mohammed, Beales, Philip, Arts, Heleen H., Munnich, Arnold, Kaplan, Josseline, Antignac, Corinne, Cormier-Daire, Valérie, Rozet, Jean-Michel
Publicado em 2012

Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome

Por Gerber, Sylvie, Alzayady, Kamil J., Burglen, Lydie, Brémond-Gignac, Dominique, Marchesin, Valentina, Roche, Olivier, Rio, Marlène, Funalot, Benoit, Calmon, Raphaël, Durr, Alexandra, Gil-da-Silva-Lopes, Vera Lucia, Ribeiro Bittar, Maria Fernanda, Orssaud, Christophe, Héron, Bénédicte, Ayoub, Edward, Berquin, Patrick, Bahi-Buisson, Nadia, Bole, Christine, Masson, Cécile, Munnich, Arnold, Simons, Matias, Delous, Marion, Dollfus, Helene, Boddaert, Nathalie, Lyonnet, Stanislas, Kaplan, Josseline, Calvas, Patrick, Yule, David I., Rozet, Jean-Michel, Fares Taie, Lucas
Publicado no Am J Hum Genet (2016)