Výsledky vyhledávání - Catherine Vignal
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Diagnosis and treatment of dural carotid-cavernous fistulas: a consecutive series of 27 patients Autor Marie Théaudin, J-P Saint-Maurice, R Chapot, Kouroche Vahedi, Mikaël Mazighi, Catherine Vignal, Guillaume Saliou, Christian Stapf, Bousser Mg, Emmanuel Houdart
Vydáno 2006Artigo -
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Safety of Intravitreal Gene Therapy for Treatment of Subjects with Leber Hereditary Optic Neuropathy due to Mutations in the Mitochondrial ND4 Gene: The REVEAL Study Autor Catherine Vignal, Jean‐François Girmens, Isabelle Audo, Saddek Mohand Saïd, Marie‐Hélène Errera, Lise Plaine, Denis O’Shaughnessy, Magali Taiel, José‐Alain Sahel
Vydáno 2021Artigo -
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Safety of rAAV2/2-ND4 Gene Therapy for Leber Hereditary Optic Neuropathy Autor Catherine Vignal, Scott Uretsky, Serge Fitoussi, Anne Galy, Laure Blouin, Jean‐François Girmens, Samuel Bidot, Nitza Thomasson, Céline Bouquet, Sonia Valero, Sandrine Meunier, Jean Philippe Combal, Bernard Gilly, Barrett Katz, José‐Alain Sahel
Vydáno 2018Artigo -
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Did the COVID-19 Pandemic Increase the Incidence of Acute Macular Neuroretinopathy? Autor Azar, Georges, Bonnin, Sophie, Vasseur, Vivien, Faure, Céline, Salviat, Flore, Clermont, Catherine Vignal, Titah, Cherif, Farès, Selim, Boulanger, Elise, Derrien, Sabine, Couturier, Aude, Duvilliers, Amélie, Manassero, Anthony, Hage, Rabih, Tadayoni, Ramin, Behar-Cohen, Francine, Mauget-Faÿsse, Martine
Vydáno 2021Text -
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Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel<i>OPA1</i>mutations Autor Marc Ferré, Dominique Bonneau, Dan Miléa, Arnaud Chevrollier, Christophe Verny, Hélène Dollfus, Carmen Ayuso, Sabine Defoort, Catherine Vignal, Xavier Zanlonghi, Jean-François Charlin, Josseline Kaplan, Sylvie Odent, Christian P. Hamel, Vincent Procaccio, Pascal Reynier, Patrizia Amati‐Bonneau
Vydáno 2009Artigo -
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MRI features of demyelinating disease associated with anti-MOG antibodies in adults Autor Marc Denève, Damien Biotti, Sofia Patsoura, M. Ferrier, Zuzana Meluchova, L. Mahieu, Françoise Héran, Catherine Vignal, Romain Deschamps, Olivier Gout, Nicolas Menjot de Champfleur, Xavier Ayrignac, Clarisse Carra‐Dallière, Pierre Labauge, Cécile Dulau, Thomas Tourdias, Hervé Dumas, Christophe Cognard, David Brassat, Fabrice Bonneville
Vydáno 2019Revisão -
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Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study Autor Valérie Biousse, Nancy J. Newman, Patrick Yu‐Wai‐Man, Valério Carelli, Mark L. Moster, Catherine Vignal, Thomas Klopstock, Alfredo A. Sadun, Robert C. Sergott, Rabih Hage, Simona Esposti, Chiara La Morgia, Claudia Priglinger, Rustum Karanja, Laure Blouin, Magali Taiel, José‐Alain Sahel
Vydáno 2020Artigo -
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International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy Autor Valério Carelli, Michele Carbonelli, I.F.M. de Coo, Aki Kawasaki, Thomas Klopstock, Wolf A. Lagrèze, Chiara La Morgia, Nancy J. Newman, Christophe Orssaud, Jan Willem R. Pott, Alfredo A. Sadun, J. van Everdingen, Catherine Vignal, Marcela Votruba, Patrick Yu‐Wai‐Man, Piero Barboni
Vydáno 2017Artigo -
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Pediatric Eye Injuries by Hydroalcoholic Gel in the Context of the Coronavirus Disease 2019 Pandemic Autor Gilles C. Martin, Gaël Le Roux, Damien Guindolet, Etienne Boulanger, Denis Hasle, Émilie Morin, Dominique Vodovar, Catherine Vignal, Éric Gabison, Alexis Descatha, Christine Tournoud, Jérôme Langrand, Hervé Laborde‐Castérot, Nicolas Franchitto, Nicolas Simon, Camille Paradis, Anne-Marie Patat, Patrick Nisse, Ramy Azzouz, Marie Deguigne, Marion Legeay
Vydáno 2021Artigo -
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Natural history of patients with Leber hereditary optic neuropathy—results from the REALITY study Autor Yu-Wai-Man, Patrick, Newman, Nancy J., Carelli, Valerio, La Morgia, Chiara, Biousse, Valérie, Bandello, Francesco M., Clermont, Catherine Vignal, Campillo, Lorena Castillo, Leruez, Stephanie, Moster, Mark L., Cestari, Dean M., Foroozan, Rod, Sadun, Alfredo, Karanjia, Rustum, Jurkute, Neringa, Blouin, Laure, Taiel, Magali, Sahel, José-Alain
Vydáno 2021Text -
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Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison Autor Nancy J. Newman, Patrick Yu‐Wai‐Man, Valério Carelli, Valérie Biousse, Mark L. Moster, Catherine Vignal, Robert C. Sergott, Thomas Klopstock, Alfredo A. Sadun, Jean‐François Girmens, Chiara La Morgia, Adam A. DeBusk, Neringa Jurkutė, Claudia Priglinger, Rustum Karanjia, Constant Josse, Julie Salzmann, François Montestruc, Michel Roux, Magali Taiel, José‐Alain Sahel
Vydáno 2021Artigo -
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Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy Autor Patrick Yu‐Wai‐Man, Nancy J. Newman, Valério Carelli, Mark L. Moster, Valérie Biousse, Alfredo A. Sadun, Thomas Klopstock, Catherine Vignal, Robert C. Sergott, Günther Rudolph, Chiara La Morgia, Rustum Karanjia, Magali Taiel, Laure Blouin, Pierre Burguière, Gerard Smits, Caroline Chevalier, Harvey Masonson, Yordak Salermo, Barrett Katz, Serge Picaud, David J. Calkins, José‐Alain Sahel
Vydáno 2020Artigo -
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Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset Autor Nancy J. Newman, Patrick Yu‐Wai‐Man, Valério Carelli, Mark L. Moster, Valérie Biousse, Catherine Vignal, Robert C. Sergott, Thomas Klopstock, Alfredo A. Sadun, Piero Barboni, Adam A. DeBusk, Jean‐François Girmens, Günther Rudolph, Rustum Karanjia, Magali Taiel, Laure Blouin, Gerard Smits, Barrett Katz, José‐Alain Sahel, Catherine Vignal, Rabih Hage, Claudia B. Catarino, Claudia Priglinger, Siegfried Priglinger, Stephan Thurau, Bettina von Livonius, Daniel Rudolf Muth, Armin Wolf, Jasmina Al-Tamami, Angelika Pressler, Cosima Schertler, Martin Hildebrandt, Michael Neuenhahn, Gad Heilweil, Irena Tsui, G. Baker Hubbard, Andrew Hendrick, Michael Dattilo, Jason H. Peragallo, Eman Hawy, Med Lindreth DuBois, Deborah Gibbs, Alcides Fernandes Filho, Jannah Dobbs, Michele Carbonelli, Lidia Di Vito, Manuela Contin, Susan Mohamed, Chiara La Morgia, Sara Silvestri, James Acheson, Maria Eleftheriadou, Simona Esposti, Maria Gemenetzi, Lauren Leitch-Devlin, William Tucker, Neringa Jurkutė, Melissa SantaMaria, Heather Tollis, Julie A. Haller, Maria Massini
Vydáno 2021Artigo -
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The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands Autor Aude Rocatcher, Valérie Desquiret‐Dumas, Majida Charif, Marc Ferré, Philippe Gohier, Delphine Mirebeau‐Prunier, Christophe Verny, Dan Miléa, Guy Lenaers, Catherine Vignal, Cédric Lamirel, Rabih Hage, Hélène Dollfus, Isabelle Meunier, Xavier Zanlonghi, Valérie Touitou, Pierre Lebranchu, Sylvie Odent, Caroline Froment Tilikete, L. Jeanjean, Sabine Defoort‐Dhellemmes, Isabelle Drumare-Bouvet, Vasily Smirnov, Catherine Vincent-Delorme, Damien Biotti, Fanny Varenne, Patrick Calvas, Nicolas Chassaing, Mikaël Cohen, Christophe Orssaud, Fanny Mochel, Agathe Roubertie, Annick Toutain, Frédéric Pollet-Villard, Marie Noelle Bonnet Dupeyron, Céline Boulicot, Béatrice Cochener, Alice Goldenberg, Marie Line Jacquemont, Christine Francannet, Dominique Bonneau, Pascal Reynier, Patrizia Amati‐Bonneau
Vydáno 2022Artigo -
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Visual Outcomes Following Plasma Exchange for Optic Neuritis: An International Multicenter Retrospective Analysis of 395 Optic Neuritis Attacks Autor John J. Chen, Eoin P. Flanagan, Sean J. Pittock, Nicole Caroline Stern, Nanthaya Tisavipat, Muhammad Tariq Bhatti, Kevin Chodnicki, Deena Tajfirouz, Sepideh Jamali, Amy Kunchok, Eric Eggenberger, Marie A. Di Nome, Elias S. Sotirchos, Eleni S. Vasileiou, Amanda D. Henderson, Anthony C. Arnold, Laura Bonelli, Heather E. Moss, Sylvia Elizabeth Villarreal Navarro, Tanyatuth Padungkiatsagul, Hadas Stiebel‐Kalish, Itay Lotan, Adi Wilf‐Yarkoni, Helen V. Danesh‐Meyer, Stefan Ivanov, Saif Huda, Mirasol Forcadela, David O. Hodge, Pascale Poullin, J. Rode, Caroline Papeix, Samir Saheb, Marine Boudot de la Motte, Catherine Vignal, Yael Hacohen, Julie Pique, Élisabeth Maillart, Romain Deschamps, Bertrand Audoin, Romain Marignier
Vydáno 2023Artigo -
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Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy Autor Sarah L. Stenton, Н Л Шеремет, Claudia B. Catarino, N.A. Andreeva, Zahra Assouline, Piero Barboni, Ortal Barel, Riccardo Berutti, Igor Bychkov, Leonardo Caporali, Mariantonietta Capristo, Michele Carbonelli, Maria Lucia Cascavilla, Peter Charbel Issa, Peter Freisinger, S. Gerber, Daniele Ghezzi, Elisabeth Graf, Juliana Heidler, Maja Hempel, Elise Héon, Y.S. Itkis, Elisheva Javasky, Josseline Kaplan, Robert Kopajtich, Cornelia Kornblum, Réka Kovács-Nagy, Tatiana Krylova, Wolfram S. Kunz, Chiara La Morgia, Costanza Lamperti, Christina Ludwig, Pedro Felipe Malacarne, Alessandra Maresca, Johannes A. Mayr, Jana Meisterknecht, Tatiana A. Nevinitsyna, Flavia Palombo, Ben Pode‐Shakked, M.S. Shmelkova, Tim M. Strom, Francesca Tagliavini, Michal Tzadok, Amelie T. van der Ven, Catherine Vignal, Matias Wagner, Ekaterina Zakharova, N.V. Zhorzholadze, Jean‐Michel Rozet, Valério Carelli, Polina G. Tsygankova, Thomas Klopstock, Ilka Wittig, Holger Prokisch
Vydáno 2021Artigo
Vyhledávací nástroje:
Související témata
Medicine
Ophthalmology
Optic nerve
Optic neuropathy
Leber's hereditary optic neuropathy
Biology
Genetics
Pathology
Gene
Internal medicine
Disease
Genetic enhancement
Visual acuity
Anatomy
Mitochondrial DNA
Multiple sclerosis
Optic neuritis
Optometry
Pediatrics
Retinal
Atrophy
Fundus (uterus)
Immunology
Medical emergency
Mitochondrial disease
Mutation
Neuromyelitis optica
Neuroscience
Papilledema
Pharmacology