Risultati della ricerca - François Viallet
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Performance of a bimanual load-lifting task by parkinsonian patients. di François Viallet, J Massion, R Massarino, Rehana Khalil
Pubblicazione 1987Artigo -
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Disease Severity and Progression in Progressive Supranuclear Palsy and Multiple System Atrophy: Validation of the NNIPPS – PARKINSON PLUS SCALE di C. Payán, François Viallet, G. Bernhard Landwehrmeyer, Muriel Bonnet, Michel Borg, Franck Durif, Lucette Lacomblez, Frédéric Bloch, Marc Verny, Jacques Fermanian, Y. Agid, Albert C. Ludolph, Peter Leigh, Gilbert Bensimon
Pubblicazione 2011Artigo -
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Repetitive Behaviours in Patients with Gilles de la Tourette Syndrome: Tics, Compulsions, or Both? di Yulia Worbe, Luc Mallet, Jean-Louis Golmard, Cécile Béhar, Franck Durif, Isabelle Jalenques, Philippe Damier, Pascal Derkinderen, Pierre Pollak, Mathieu Anheim, E. Broussolle, Jing Xie, Valérie Mesnage, Karl Mondon, François Viallet, Pierre Jedynak, Mouna Ben Djebara, Michaël Schüpbach, Antoine Pélissolo, Marie Vidailhet, Y. Agid, Jean Luc Houeto, Andréas Hartmann
Pubblicazione 2010Artigo -
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Do Acoustic Characteristics of Dysarthria in People With Parkinson's Disease Differ Across Languages? di Serge Pinto, Rita Cardoso, Cyril Atkinson‐Clement, Isabel Guimarães, Jasmin Sadat, Helena Santos, Céline Mercier, Joana Carvalho, Marie‐Charlotte Cuartero, Pedro Oliveira, Pauline Welby, Sónia Frota, Émilie Cavazzini, Marina Vigário, Alban Letanneux, Marisa Cruz, Coralie Brulefert, Morgane Desmoulins, Isabel Pavão Martins, Rui Rothe‐Neves, François Viallet, Joaquim J. Ferreira
Pubblicazione 2024Artigo -
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Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort di Suzanne Lesage, Marion Houot, Graziella Mangone, Christelle Tesson, Hélène Bertrand, Sylvie Forlani, Mathieu Anheim, Christine Brefel‐Courbon, Emmanuel Broussolle, Stéphane Thobois, Philippe Damier, Franck Durif, Emmanuel Roze, François Tison, David Grabli, Fabienne Ory‐Magne, Bertrand Degos, François Viallet, Florence Cormier‐Dequaire, Anne-Marie Ouvrard-Hernandez, Marie Vidailhet, Ebba Lohmann, Andrew Singleton, Jean‐Christophe Corvol, Alexis Brice
Pubblicazione 2020Artigo -
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Characterization of Recessive Parkinson Disease in a Large Multicenter Study di Suzanne Lesage, Ariane Lunati, Marion Houot, Sawssan Ben Romdhan, Fabienne Clot, Christelle Tesson, Graziella Mangone, Benjamin Le Toullec, Thomas Courtin, Kathy Larcher, Mustapha Benmahdjoub, Mohamed Arezki, Ahmed Bouhouche, Mathieu Anheim, Emmanuel Roze, François Viallet, François Tison, Emmanuel Broussolle, Murat Emre, Haşmet Hanağası, Başar Bılgıç, Mériem Tazir, Mouna Ben Djebara, Riadh Gouider, Christine Tranchant, Marie Vidailhet, E. Le Guern, Olga Corti, Chokri Mhiri, Ebba Lohmann, Andrew Singleton, Jean‐Christophe Corvol, Alexis Brice
Pubblicazione 2020Artigo -
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Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans di Suzanne Lesage, Étienne Patin, Christel Condroyer, Anne‐Louise Leutenegger, Ebba Lohmann, Nir Giladi, Anat Bar‐Shira, Soraya Belarbi, Nassima Hecham, Pierre Pollak, Anne-Marie Ouvrard-Hernandez, Soraya Bardien, Jonathan Carr, Traki Benhassine, Hiroyuki Tomiyama, Caroline Pirkevi, Tarik Hamadouche, Cécile Cazeneuve, A. Nazlı Başak, Nobutaka Hattori, Alexandra Dürr, Mériem Tazir, Avi Orr‐Urtreger, Lluís Quintana‐Murci, Alexis Brice, Y. Agid, Muriel Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Ph. Damier, A. Destée, Alexandra Dürr, F. Durif, Ebba Lohmann, María Martínez, Clotilde Penet, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, André R. Troiano, Marc Vérin, François Viallet, Marie Vidailhet
Pubblicazione 2010Artigo -
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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population di Mohamad Saad, Suzanne Lesage, Aude Saint-Pierre, Jean‐Christophe Corvol, Diana Zélénika, Jean‐Charles Lambert, Marie Vidailhet, George D. Mellick, Ebba Lohmann, F. Durif, Pierre Pollak, Philippe Damier, François Tison, Peter A. Silburn, Christophe Tzourio, Sylvie Forlani, Marie‐Anne Loriot, Maurice Giroud, Catherine Helmer, Florence Portet, Philippe Amouyel, Mark Lathrop, Alexis Elbaz, Alexandra Dürr, María Martínez, Alexis Brice, Y. Agid, Mathieu Anheim, Muriel Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Jean‐Christophe Corvol, Philippe Damier, A. Destée, Alexandra Dürr, F. Durif, Sonja Klebe, Ebba Lohmann, María Martínez, Christiane Penet, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, Marc Vérin, François Viallet, Marie Vidailhet
Pubblicazione 2010Artigo -
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Clopidogrel Plus Aspirin Versus Warfarin in Patients With Stroke and Aortic Arch Plaques di Pierre Amarenco, Stephen M. Davis, E. Jones, Ariel Cohen, Wolf‐Dieter Heiss, Markku Kaste, Cédric Laouénan, Dennis Young, Malcolm Macleod, Geoffrey A. Donnan, Christopher F. Bladin, Brian R. Chambers, Judith Frayne, Graeme J. Hankey, Christopher Levi, Stephen Read, Philippe Ravaud, Turgut Tatlisumak, Lauri Soinne, Mika Laine, Mikko Syvänne, Pirkka Vikatmaa, Mauri Lepäntalo, France Mentré, Simon Gosset, Leonid Churilov, T. de Broucker, Pascal Favrole, Jérôme Mawet, Yves Mocquard, Michaël Obadia, Olivier Godefroy, Hassan Hosseini, Fernando Pico, Pierre Garnier, Marcel Malbec, Jean‐François Pinel, Olivier Ille, Xavier Vadamme, Francisco Macian-Montoro, Jérôme Servan, François Viallet, Thierry Rosolacci, Patrick Lecoz, Pierre Clavelou, Olivier Detante, Tae‐Hee Cho, D. Saudeau, Patrik Michel, Suzette D’Ombrogio, David J. Serisier, Jonathon Sturm, Thomas Kimber, Romesh Marcus, Ray Schwartz, Rob Helme, David Blacker, Jonathan Wood
Pubblicazione 2014Artigo -
11
Levodopa-carbidopa intestinal gel in advanced Parkinson's: Final results of the GLORIA registry di Angelo Antonini, Werner Poewe, К. Ray Chaudhuri, Robert Jech, Barbara Pickut, Zvezdan Pirtošek, József Attila Szász, Francesc Valldeoriola, Christian Winkler, Lars Bergmann, Ashley Yegin, Koray Onuk, David Barch, Per Odin, Ene Amalia, G. Arnold, Ovidiu Băjenaru, Bruno Bergmans, Kari Anne Bjørnarå, Jeff Blackie, Matthias Bode, Paul Bourgeois, Stephan Bohlhalter, Ioan Buraga, Pierre R. Burkhard, Philippe Busson, Matilde Calopa, Jesper O. Clausen, Erik Hvid Danielsen, Luc Defebvre, Valérie Delvaux, Sophie Dethy, Espen Dietrichs, Oriol de Fábregues, Ransmayr Gerhard, Graziano Gusmaroli, Kirsten Hahn, Björn Hauptmann, Tove Henriksen, Jorge Hernández‐Vara, Anne Jeanjean, Michaela Kaiserová, Jan Kassubek, Thomas Kimber, Spyridon Konitsiotis, Rejko Krüger, Jaime Kulisevsky, Jo Leenders, Christofer Lundqvist, Frédéric Magné, Pietro Marano, Ivan Milanov, Nicola Modugno, Anjum Misbahuddin, Martin Nevrlý, Zikos Panayiotis, Kenn Freddy Pedersen, Stephen Wørlich Pedersen, Lăcrămioara Perju‐Dumbravă, Mirthe M. Ponsen, Bogdan Ovidiu Popescu, Michel Rijntjes, Vıctor Puente, Christoph Redecker, Christoph Schrader, Mariachiara Sensi, Mihaela Simu, Cleanthe Spanaki, Alexander Storch, Anette Storstein, Volker Tomantschger, Chris van der Linden, Teus van Laar, François Viallet, Tatiana Witjas, Martin Wolz, Maurizio Zibetti, Michel Van Zandijcke
Pubblicazione 2017Artigo -
12
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy di Suzanne Lesage, Valérie Drouet, Elisa Majounie, Vincent Deramecourt, Maxime Jacoupy, Aude Nicolas, Florence Cormier‐Dequaire, Sidi Mohamed Hassoun, Claire Pujol, Sorana Ciura, Zoi Erpapazoglou, Tatiana Usenko, Claude‐Alain Maurage, Mourad Sahbatou, Stefan Liebau, Joshua Shulman, Başar Bılgıç, Murat Emre, Nihan Erginel‐Ünaltuna, Gamze Güven, François Tison, Christine Tranchant, Marie Vidailhet, Jean‐Christophe Corvol, Paul Krack, Anne‐Louise Leutenegger, Michael A. Nalls, Dena G. Hernandez, Peter Heutink, J. Raphael Gibbs, John Hardy, Nicholas Wood, Thomas Gasser, Alexandra Dürr, Jean‐François Deleuze, Mériem Tazir, A. Destée, Ebba Lohmann, Edor Kabashi, Andrew Singleton, Olga Corti, Alexis Brice, Suzanne Lesage, François Tison, Marie Vidailhet, Jean‐Christophe Corvol, Y. Agid, Mathieu Anheim, Anne-Marie Bonnet, Michel Borg, Emmanuel Broussolle, Philippe Damier, A. Destée, Alexandra Dürr, Franck Durif, Paul Krack, Stephan Klebe, Ebba Lohmann, María Martínez, Pierre Pollak, Olivier Rascol, Christine Tranchant, Marc Vérin, François Viallet, Alexis Brice, Suzanne Lesage, Elisa Majounie, François Tison, Marie Vidailhet, Jean‐Christophe Corvol, Michael A. Nalls, Dena G. Hernandez, J. Raphael Gibbs, Alexandra Dürr, Sampath Arepalli, Roger A. Barker, Yoav Ben‐Shlomo, Daniela Berg, Francesco Bettella, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, Bastiaan R. Bloem, Zoltán Bochdanovits, Michael Bonin, Suzanne Lesage, François Tison, Marie Vidailhet, Jean‐Christophe Corvol, Y. Agid, Mathieu Anheim, Anne-Marie Bonnet, Michel Borg, Emmanuel Broussolle, Philippe Damier, A. Destée, Alexandra Dürr, Franck Durif, Paul Krack, Stephan Klebe
Pubblicazione 2016Artigo -
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Large-scale replication and heterogeneity in Parkinson disease genetic loci di Manu Sharma, John P. A. Ioannidis, Jan Aasly, Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Lars Bertram, Maria Bozi, David Crosiers, Carl E Clarke, Maurizio Facheris, Matthew J. Farrer, Gaëtan Garraux, Suzana Gispert, Georg Auburger, Carles Vilariño‐Güell, Georgios M. Hadjigeorgiou, Andrew A. Hicks, Nobutaka Hattori, Beom S. Jeon, Suzanne Lesage, Christina M. Lill, Juei-Jueng Lin, Timothy Lynch, Peter Lichtner, Anthony E. Lang, Vincent Mok, Barbara Jasińska‐Myga, George D. Mellick, Karen Morrison, Grzegorz Opala, Peter P. Pramstaller, Irene Pichler, Sung Sup Park, Aldo Quattrone, Ekaterina Rogaeva, Owen A. Ross, Leonidas Stefanis, Joanne Stockton, Wataru Satake, Peter A. Silburn, Jessie Theuns, Eng-King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Ryan J. Uitti, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Kuo-Chu Yueh, Yi Zhao, Thomas Gasser, Demetrius M. Maraganore, Rejko Krüger, R.S Boyle, A Sellbach, John D. O’Sullivan, Greg T. Sutherland, G. Siebert, N. Dissanayaka, Christine Van Broeckhoven, Jessie Theuns, David Crosiers, Barbara Pickut, Sebastiaan Engelborghs, Bram Meeus, Peter Paul De Deyn, Patrick Cras, Ekaterina Rogaeva, Anthony E. Lang, Y. Agid, Mathieu Anheim, A-M Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Jean‐Christophe Corvol, Philippe Damier, A. Destée, Alexandra Dürr, F. Durif, Suzanne Lesage, Ebba Lohmann, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, François Viallet, Marie Vidailhet, Christophe Tzourio, Philippe Amouyel, Marie‐Anne Loriot, Eugénie Mutez, Aurélie Duflot, Jean-Philippe Legendre, Nawal Waucquier, Thomas Gasser, Olaf Rieß, Daniela Berg, Claudia Schulte
Pubblicazione 2012Artigo -
14
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism di Sonja Klebe, Jean Louis Golmard, Michael A. Nalls, Mohamad Saad, Andrew B. Singleton, José Brás, John Hardy, Javier Simón‐Sánchez, Peter Heutink, Gregor Kuhlenbäumer, Rim Charfi, Christine Klein, J. Hagenah, Thomas Gasser, Isabel Wurster, Suzanne Lesage, D. Lorenz, Günther Deuschl, F. Durif, Pierre Pollak, Philippe Damier, François Tison, A. Dürr, Philippe Amouyel, Jean‐Charles Lambert, Christophe Tzourio, C. Maubaret, Fanny Charbonnier‐Beaupel, Khadija Tahiri, Marie Vidailhet, María Martínez, Alexis Brice, Jean‐Christophe Corvol, Y. Agid, Mathieu Anheim, Muriel Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Jean‐Christophe Corvol, Philippe Damier, A. Destée, A. Dürr, Franck Durif, Sonja Klebe, Ebba Lohmann, María Martínez, Christiane Penet, Pierre Pollak, Paul Krack, Olivier Rascol, François Tison, Christine Tranchant, Marc Vérin, François Viallet, Vincent Plagnol, José Brás, D. G. Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Philippe Amouyel, Sampath Arepalli, Guido P. H. Band, Roger A. Barker, C. Bellinguez, Yoav Ben‐Shlomo, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, B.R. Bloem, Zoltán Bochdanovits, Marina de Nadai Bonin Gomes, Kathrin Brockmann, Janet Brooks, David J. Burn, Gavin Charlesworth, Honglei Chen, Patrick F. Chinnery, S. A. Chong, C. E. Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, J.-F. Dartigues, P. Deloukas, David T. Dexter, Karin D. van Dijk, Allissa Dillman, Franck Durif, Sarah Edkins, Jonathan Evans
Pubblicazione 2013Artigo
Strumenti per la ricerca:
Soggetti correlati
Medicine
Biology
Gene
Genetics
Internal medicine
Disease
Parkinson's disease
Psychology
Phenotype
Allele
Genotype
Parkinsonism
Psychiatry
Cohort
Computer science
Developmental psychology
Gastroenterology
Genetic association
Genome-wide association study
LRRK2
Mutation
Neuroscience
Physical medicine and rehabilitation
Physical therapy
Population
Single-nucleotide polymorphism
Allele frequency
Anatomy
Aorta
Aortic arch