نتائج البحث - Jean‐Philippe Azulay

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  1. 1
    Comparative analysis of gait and speech in Parkinson's disease: hypokinetic or dysrhythmic disorders?

    Comparative analysis of gait and speech in Parkinson's disease: hypokinetic or dysrhythmic disorders? حسب S. Cantiniaux, M. Vaugoyeau, D Robert, C. Horrelou-Pitek, Julien Mancini, Tatiana Witjas, Jean‐Philippe Azulay

    منشور في 2009
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  2. 2
    A prospective single-blind study of Gamma Knife thalamotomy for tremor

    A prospective single-blind study of Gamma Knife thalamotomy for tremor حسب Tatiana Witjas, Romain Carron, Paul Krack, Alexandre Eusébio, Marianne Vaugoyeau, Marwan Hariz, Jean Philippe Azulay, Jean Régis

    منشور في 2015
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  3. 3
    The human subthalamic nucleus encodes the subjective value of reward and the cost of effort during decision-making

    The human subthalamic nucleus encodes the subjective value of reward and the cost of effort during decision-making حسب Alexandre Zénon, Yann Duclos, Romain Carron, Tatiana Witjas, Christelle Baunez, Jean Régis, Jean‐Philippe Azulay, Peter Brown, Alexandre Eusébio

    منشور في 2016
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  4. 4
    Resonance in subthalamo-cortical circuits in Parkinson's disease

    Resonance in subthalamo-cortical circuits in Parkinson's disease حسب Alexandre Eusébio, Alek Pogosyan, Shouyan Wang, Bruno B. Averbeck, Louise Doyle Gaynor, S. Cantiniaux, Tatiana Witjas, Patricia Limousin, Jean‐Philippe Azulay, Peter Brown

    منشور في 2009
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  5. 5
    Neuroendocrine Disturbances in Huntington's Disease

    Neuroendocrine Disturbances in Huntington's Disease حسب Nadine Saleh, Stéphane Moutereau, Alexandra Dürr, Pierre Krystkowiak, Jean‐Philippe Azulay, Christine Tranchant, Emmanuel Broussolle, Françoise Morin, Anne‐Catherine Bachoud‐Lévi, Patrick Maison

    منشور في 2009
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  6. 6
    Economic Burden of Parkinson’s Disease: A Multinational, Real-World, Cost-of-Illness Study

    Economic Burden of Parkinson’s Disease: A Multinational, Real-World, Cost-of-Illness Study حسب К. Ray Chaudhuri, Jean‐Philippe Azulay, Per Odin, Susanna Lindvall, Josefa Domingos, Ali Alobaidi, Prasanna L. Kandukuri, Vivek S. Chaudhari, Juan Carlos Parra, Toru Yamazaki, Julia Oddsdottir, Jack Wright, Pablo Martínez‐Martín

    منشور في 2024
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  7. 7
    Beta burst coupling across the motor circuit in Parkinson's disease

    Beta burst coupling across the motor circuit in Parkinson's disease حسب Gerd Tinkhauser, Flavie Torrecillos, Yann Duclos, Huiling Tan, Alek Pogosyan, Petra Fischer, Romain Carron, Marie‐Laure Welter, Carine Karachi, Wim Vandenberghe, Bart Nuttin, Tatiana Witjas, Jean Régis, Jean‐Philippe Azulay, Alexandre Eusébio, Peter Brown

    منشور في 2018
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  8. 8
    MUSK, a new target for mutations causing congenital myasthenic syndrome

    MUSK, a new target for mutations causing congenital myasthenic syndrome حسب Frédéric Chevessier, Brice Faraut, Aymeric Ravel‐Chapuis, Pascale Richard, Karen Gaudon, Stéphanie Bauché, Cassandra Prioleau, Ruth Herbst, Evelyne Goillot, Christine Ioos, Jean‐Philippe Azulay, Shahram Attarian, Jean‐Paul Leroy, Emmanuel Fournier, Claire Legay, Laurent Schaeffer, Jeanine Koenig, Michel Fardeau, B. Eymard, Jean Pouget, Daniel Hantaı̈

    منشور في 2004
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  9. 9
    CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

    CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5 حسب Cyril Goizet, A. Boukhris, A. Dürr, Christian Beetz, Jérémy Truchetto, Christelle Tesson, Maria K. Tsaousidou, Sylvie Forlani, Lucie Guyant‐Maréchal, B. Fontaine, João Tiago Guimarães, Bertrand Isidor, O. Chazouillères, Dominique Wendum, Djamel Grid, Françoise Chevy, Patrick F. Chinnery, Paula Coutinho, Jean‐Philippe Azulay, Imed Feki, Fanny Mochel, Claude Wolf, Chokri Mhiri, Andrew H. Crosby, Alexis Brice, Giovanni Stévanin

    منشور في 2009
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  10. 10
    Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia

    Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia حسب Jean‐Loup Méreaux, Guillaume Banneau, Mélanie Papin, Giulia Coarelli, Rémi Valter, Laure Raymond, Bophara Kol, Olivier Ariste, Livia Parodi, Laurène Tissier, Mathilde Mairey, Samia Ait Said, Celia Gautier, Marine Guillaud-Bataille, Mathieu Anheim, Jean‐Philippe Azulay, Odile Boesfplug-Tanguy, Perrine Charles, Alexandra Dürr, Cyril Goizet, Didier Hannequin, Vincent Huin, Michel Kœnig, Pierre Labauge, Eric Leguern, Karine Nguyen, Mathilde Renaud, Diana Rodriguez, Christophe Verny, Sylvie Forlani, Pierre de la Grange, Alexis Brice, Giovanni Vazza, Alexandra Dürr, Eric Leguern, Giovanni Stévanin

    منشور في 2021
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  11. 11
    Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson’s disease

    Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson’s disease حسب Caroline Moreau, Sayah Meguig, Jean‐Christophe Corvol, Julien Labreuche, Francis Vasseur, Alain Duhamel, Arnaud Delval, Thomas Bardyn, Jean‐Christophe Devedjian, Nathalie Rouaix, G. Petyt, Christine Brefel‐Courbon, Fabienne Ory‐Magne, Dominique Guehl, Alexandre Eusébio, Valérie Fraix, Pierre‐Jean Saulnier, Ouhaïd Lagha‐Boukbiza, F. Durif, Mirela Faighel, Caroline Giordana, Sophie Drapier, David Maltête, Christine Tranchant, Jean Luc Houeto, Bettina Debû, Jean-Philippe Azulay, François Tison, A. Destée, Marie Vidailhet, Olivier Rascol, Kathy Dujardin, Luc Defebvre, Régis Bordet, Bernard Sablonnière, David Devos

    منشور في 2015
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  12. 12
    Trial of Prasinezumab in Early-Stage Parkinson’s Disease

    Trial of Prasinezumab in Early-Stage Parkinson’s Disease حسب Gennaro Pagano, Kirsten I. Taylor, Judith Anzures‐Cabrera, Maddalena Marchesi, Tanya Simuni, Kenneth Marek, Ronald B. Postuma, Nicola Pavese, Fabrizio Stocchi, Jean‐Philippe Azulay, Brit Mollenhauer, Lydia López Manzanares, David Russell, James T. Boyd, Anthony P. Nicholas, M.R. Luquin, Robert A. Hauser, Thomas Gasser, Werner Poewe, Benedicte Ricci, Anne Boulay, Annamarie Vogt, Frank Boess, Juergen Dukart, Giulia D’Urso, Rebecca Finch, Stefano Zanigni, Annabelle Monnet, Nathalie Pross, Andrea Hahn, Hanno Svoboda, Markus Britschgi, Florian Lipsmeier, Ekaterina Volkova-Volkmar, Michael Lindemann, Sebastian Dziadek, Štefan Holiga, Daria Rukina, Thomas Kustermann, Geoffrey A. Kerchner, Paulo Fontoura, Daniel Umbricht, Rachelle S. Doody, Tania Nikolcheva, Azad Bonni

    منشور في 2022
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  13. 13
    CSF neurofilament light chain and phosphorylated tau 181 predict disease progression in PSP

    CSF neurofilament light chain and phosphorylated tau 181 predict disease progression in PSP حسب Julio C. Rojas, Jee Bang, Iryna Lobach, Richard Tsai, Gil D. Rabinovici, Bruce L. Miller, Adam L. Boxer, David R. Williams, Anne Lafontaine, Connie Marras, Mandar Jog, Michael Panisset, Anthony E. Lang, Lesley H. Parker, Alistair Stewart, Jean‐Christophe Corvol, Jean‐Philippe Azulay, Philippe Couratier, Brit Mollenhauer, Stefan Lorenzl, Albert Ludolph, R. Benecke, Günter U. Höglinger, Axel Lipp, Heinz Reichmann, Dirk Woitalla, Dennis Chan, Adam Zermansky, David J. Burn, Andrew J. Lees, Illana Gozes, Adam L. Boxer, Bruce L. Miller, Iryna Lobach, Erik D. Roberson, Lawrence S. Honig, Edward Zamrini, Rajesh Pahwa, Yvette Bordelon, Erika Driver-Dunkley, Stephanie Lessig, Mark Lew, Kyle Womack, Bradley F. Boeve, Joseph M. Ferrara, Argyle Hillis, Daniel Kaufer, Rajeev Kumar, Tao Xie, Steven A. Gunzler, Theresa Zesiewicz, Praveen Dayalu, Lawrence I. Golbe, Murray Grossman, Joseph Jankovic, Scott McGinnis, Anthony Santiago, Paul Tuite, Stuart Isaacson, Julie Leegwater‐Kim, Irene Litvan, David S. Knopman, Lon S. Schneider, Rachelle S. Doody, Mary Koestler, Clifford R. Jack, Viviana Van Deerlin, Christopher Randolph, Steve Whitaker, Joe Hirman, Michael Gold, Bruce H. Morimoto

    منشور في 2017
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  14. 14
    Progression of brain atrophy in PSP and CBS over 6 months and 1 year

    Progression of brain atrophy in PSP and CBS over 6 months and 1 year حسب Shubir Dutt, Richard J. Binney, Hilary W. Heuer, Phi Luong, Suneth Attygalle, Priyanka Bhatt, Gabe Marx, Jonathan Elofson, Maria Carmela Tartaglia, Irene Litvan, Scott M. McGinnis, Bradford C. Dickerson, John Kornak, Dana Waltzman, Lisa Voltarelli, Norbert Schuff, Gil D. Rabinovici, Joel H. Kramer, Clifford R. Jack, Bruce L. Miller, Howard J. Rosen, Adam L. Boxer, David R. Williams, Anne Lafontaine, Connie Marras, Mandar Jog, Michael Panisset, Anthony E. Lang, Lesley H. Parker, Alistair Stewart, Jean‐Christophe Corvol, Jean‐Philippe Azulay, Philippe Couratier, Brit Mollenhauer, Stefan Lorenzl, Albert Ludolph, R. Benecke, Günter U. Höglinger, Axel Lipp, Heinz Reichmann, Dirk Woitalla, Dennis Chan, Adam Zermansky, David J. Burn, Andrew J. Lees, Illana Gozes, Adam L. Boxer, Bruce L. Miller, Iryna Lobach, Erik D. Roberson, Lawrence S. Honig, Edward Zamrini, Rajesh Pahwa, Yvette Bordelon, Erika Driver-Dunkley, Stephanie Lessig, Mark Lew, Kyle Womack, Bradley F. Boeve, Joseph M. Ferrara, Argyle Hillis, Daniel Kaufer, Rajeev Kumar, Tao Xie, Steven A. Gunzler, Theresa Zesiewicz, Praveen Dayalu, Lawrence I. Golbe, Murray Grossman, Joseph Jankovic, Scott McGinnis, A. Parra Santiago, Paul Tuite, Stuart Isaacson, Julie Leegwater‐Kim, Irene Litvan, David S. Knopman, Lon S. Schneider, Rachelle S. Doody, Mary Koestler, Clifford R. Jack, Viviana Van Deerlin, Christopher Randolph, Steve Whitaker, Joe Hirman, Michael Gold, Bruce H. Morimoto

    منشور في 2016
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  15. 15
    Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype

    Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype حسب Lou Grangeon, David Wallon, Camille Charbonnier, Olivier Quenez, Anne‐Claire Richard, Stéphane Rousseau, Clara Budowski, Thibaud Lebouvier, Anne-Gaëlle Corbillé, Marie Vidailhet, Aurélie Méneret, Emmanuel Roze, Mathieu Anheim, Christine Tranchant, Pascal Favrole, Jean‐Christophe Antoine, Luc Defebvre, Xavier Ayrignac, Pierre Labauge, Jérémie Pariente, Michel Clanet, David Maltête, Anne Rovelet‐Lecrux, Anne Boland, Jean‐François Deleuze, Pascal Favrole, Christophe Verny, Pierre Krystkowiak, Ludivine Chamard, Sébastien Moutton, Cyril Goizet, Claude Férec, Serge Timsit, S. Schaeffer, Nathalie Derache, Gilles Defer, Franck Durif, François Sellal, Olivier Rouaud, Christel Thauvin‐Robinet, Stéphanie Cubizolle, Mathilde Sauvée, Amélie Leblanc, Alexis Demas, Alice Poisson, Elisabeth Tournier‐Lasserve, Dominique Hervé, Hugues Chabriat, Guillaume Grolez, Nicolas Carrière, Luc Defebvre, Thibaud Lebouvier, Tatiana Witjas, Jean‐Philippe Azulay, Frédérique Fluchère, Mira Didic, Karine Nguyen, Mahmoud Charif, Xavier Ayrignac, Pierre Labauge, C. Lionnet, Cécilia Marelli, Simon Gaud, Tiphaine Rouaud, Brice Laurens, Emmanuelle Folgoas, Bertrand Isidor, Jean Chiésa, Maud Pallix-Guyot, Nicolas Gaillard, Nadège Olivier, Snejana Jurici, Isabelle Marey, Perrine Charles, Claire Ewenczyck, Alexandra Dürr, Cécile Hubsch, Aurélie Méneret, Marie Vidailhet, Yann Nadjar, Isabelle Le Ber, David Grabli, Emmanuel Roze, Vincent Navarro, Sylvie Mecharles-Darrigol, Julien Lagarde, Marie Sarazin, Marc Vérin, Romain Lefaucheur, David Maltête, David Wallon, Didier Hannequin, Olivier Martinaud, Lucie Guyant‐Maréchal, Gaël Nicolas, Thierry Frébourg, Anne‐Claire Richard, Dominique Campion, Olivier Guillin, Marion Yger

    منشور في 2019
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  16. 16
    Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

    Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment حسب Thomas Roux, Mathieu Barbier, Mélanie Papin, Claire-Sophie Davoine, Sabrina Sayah, Giulia Coarelli, Perrine Charles, Cécilia Marelli, Livia Parodi, Christine Tranchant, Cyril Goizet, Stephan Klebe, Ebba Lohmann, Lionel Van Maldergem, Christine Van Broeckhoven, Marie Coutelier, Christelle Tesson, Giovanni Stévanin, Charles Duyckaerts, Alexis Brice, Alexandra Dürr, Alexandra Durr, Giovanni Stévanin, Alexis Brice, Frédéric Darios, Sylvie Forlani, Pitié-Salpêtrière Site, Guillaume Banneau, Cécile Cazeneuve, Perrine Charles, Charles Duyckaerts, Bertrand Fontaine, Jean‐Philippe Azulay, Odile Boesfplug-Tanguy, Cyril Goizet, Didier Hannequin, Jamïlé Hazan, Andrea Burgo, Christophe Verny, M. Kœnig, Pierre Labauge, Cécilia Marelli, Karine N’guyen, Diana Rodriguez, Soraya Belarbi, Abdelmadjid Hamri, Mériem Tazir, Sylvia Boesch, Massimo Pandolfo, Jardim Laura, Velina Guergueltcheva, Ivalo Tournev, Olga Lucia Pedraza Linarès, Jørgen E. Nielsen, Kirsten Svenstrup, Maha S. Zaki, Peter Bauer, Lüdger Schöls, Rebecca Schüle, Alexander Lossos, Maria-Teresa Bassi, Manuela Basso, Enrico Bertini, Alfredo Brusco, Carlo Casali, Giorgio Casari, Chiara Criscuolo, Alessandro Filla, Laura Orsi, Filippo M. Santorelli, Enza Maria Valente, Marinela Vavla, Giovanni Vazza, André Mégarbané, Ali Benomar, Berry Kremer, Willeke M. C. van Roon‐Mom, Richard Roxburgh, Anne Kjersti Erichsen, Chantal Tallaksen, Isabel Alonso, Paula Coutinho, José Léal Loureiro, Jorge Sequeiros, Mustapha Salih, Vladimir Kostić, Idoia Rouco Axpe, Liena E. O. Elsayed, Martin Paucar, Samir Roumani, Soong Bing-Wen, Evan Reid, Suran Nethisinghe, Thomas T. Warner, Nicholas Wood

    منشور في 2020
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  17. 17
    Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

    Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment حسب Thomas Roux, Mathieu Barbier, Mélanie Papin, Claire-Sophie Davoine, Sabrina Sayah, Giulia Coarelli, Perrine Charles, Cécilia Marelli, Livia Parodi, Christine Tranchant, Cyril Goizet, Stephan Klebe, Ebba Lohmann, Lionel Van Maldergem, Christine Van Broeckhoven, Marie Coutelier, Christelle Tesson, Giovanni Stévanin, Charles Duyckaerts, Alexis Brice, Alexandra Dürr, Alexandra Dürr, Giovanni Stévanin, Alexis Brice, Frédéric Darios, Sylvie Forlani, Pitié-Salpêtrière Site, Guillaume Banneau, Cécile Cazeneuve, Perrine Charles, Charles Duyckaerts, Bertrand Fontaine, Jean‐Philippe Azulay, Odile Boesfplug-Tanguy, Cyril Goizet, Didier Hannequin, Jamïlé Hazan, Andrea Burgo, Christophe Verny, Michel Kœnig, Pierre Labauge, Cécilia Marelli, Karine Nguyen, Diana Rodriguez, Soraya Belarbi, Abdelmadjid Hamri, Meriem Tazir, Sylvia Boesch, Massimo Pandolfo, Jardim Laura, Velina Guergueltcheva, Ivalo Tournev, Olga Lucia Pedraza Linarès, Jørgen E. Nielsen, Kirsten Svenstrup, Maha S. Zaki, Peter Bauer, Lüdger Schöls, Rebecca Schüle, Alexander Lossos, Maria-Teresa Bassi, Manuela Basso, Enrico Bertini, Alfredo Brusco, Carlo Casali, Giorgio Casari, Chiara Criscuolo, Alessandro Filla, Laura Orsi, Filippo M. Santorelli, Enza Maria Valente, Marinela Vavla, Giovanni Vazza, André Mégarbané, Ali Benomar, Berry Kremer, Willeke M. C. van Roon‐Mom, Richard Roxburgh, Anne Kjersti Erichsen, Chantal Tallaksen, Isabel Alonso, Paula Coutinho, José L. Loureiro, Jorge Sequeiros, Mustapha Salih, Vladimir Kostić, Idoia Rouco Axpe, Liena E. O. Elsayed, Martin Paucar, Samir Roumani, Soong Bing-Wen, Evan Reid, Suran Nethisinghe, Thomas T. Warner, Nicholas Wood

    منشور في 2020
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