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Christophe Orssaud

Showing results (31-40 of 42) with videos related to

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Frontiers in Neurology|June 8, 2011
Medio-lateral postural instability in subjects with tinnitusZoi Kapoula, Qing Yang, Thanh-Thuan Lê, et al.
Acta Ophthalmologica Scandinavica|September 13, 2006
Non-penetrating deep sclerectomy for glaucoma associated with Sturge-Weber syndromeFrançois Audren, Olivia Abitbol, Pascal Dureau, et al.
Neuro-Ophthalmology (Aeolus Press)|February 5, 2026
An Apparently Isolated Optic Neuropathy Associated with Biallelic Variants in <i>SLC25A46</i> Gene Encoding the Mitochondrial Ugo1-Like ProteinPascal Reynier, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, et al.
Orphanet Journal of Rare Diseases|February 19, 2018
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathyStéphanie Leruez, Christophe Verny, Dominique Bonneau, et al.
Human Molecular Genetics|January 13, 2021
A plasma metabolomic signature of Leber hereditary optic neuropathy showing taurine and nicotinamide deficienciesCinzia Bocca, Victor Le Paih, Juan Manuel Chao de la Barca, et al.
Survey of Ophthalmology|April 30, 2026
Omics in hereditary optic neuropathies:A systematic review of clinical studies with an integrated point of viewRaoul K Khanna, Xuehao Cui, David Chuen Soong Wong, et al.
Molecular Vision|December 15, 2006
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndromeVeronique Vieira, Gabriel David, Olivier Roche, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 10, 2017
International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic NeuropathyValerio Carelli, Michele Carbonelli, Irenaeus F de Coo, et al.
Plos One|August 11, 2012
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathyAlessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
American Journal of Human Genetics|April 17, 2012
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutationsIsabelle Perrault, Sophie Saunier, Sylvain Hanein, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Frontiers in Neurology|June 8, 2011
Medio-lateral postural instability in subjects with tinnitusZoi Kapoula, Qing Yang, Thanh-Thuan Lê, et al.
Acta Ophthalmologica Scandinavica|September 13, 2006
Non-penetrating deep sclerectomy for glaucoma associated with Sturge-Weber syndromeFrançois Audren, Olivia Abitbol, Pascal Dureau, et al.
Neuro-Ophthalmology (Aeolus Press)|February 5, 2026
An Apparently Isolated Optic Neuropathy Associated with Biallelic Variants in <i>SLC25A46</i> Gene Encoding the Mitochondrial Ugo1-Like ProteinPascal Reynier, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, et al.
Orphanet Journal of Rare Diseases|February 19, 2018
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathyStéphanie Leruez, Christophe Verny, Dominique Bonneau, et al.
Human Molecular Genetics|January 13, 2021
A plasma metabolomic signature of Leber hereditary optic neuropathy showing taurine and nicotinamide deficienciesCinzia Bocca, Victor Le Paih, Juan Manuel Chao de la Barca, et al.
Survey of Ophthalmology|April 30, 2026
Omics in hereditary optic neuropathies:A systematic review of clinical studies with an integrated point of viewRaoul K Khanna, Xuehao Cui, David Chuen Soong Wong, et al.
Molecular Vision|December 15, 2006
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndromeVeronique Vieira, Gabriel David, Olivier Roche, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 10, 2017
International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic NeuropathyValerio Carelli, Michele Carbonelli, Irenaeus F de Coo, et al.
Plos One|August 11, 2012
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathyAlessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
American Journal of Human Genetics|April 17, 2012
Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutationsIsabelle Perrault, Sophie Saunier, Sylvain Hanein, et al.
Pageof 5