Search Results - "TISON, François"

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    Disease progression and prognostic factors in multiple system atrophy: A prospective cohort study by Foubert-Samier, Alexandra, Pavy-Le Traon, Anne, Guillet, Florian, Le-Goff, Mélanie, Helmer, Catherine, Tison, François, Rascol, Olivier, Proust-Lima, Cécile, Meissner, Wassilios G.

    Published in Neurobiology of disease (01-06-2020)
    “…Multiple system atrophy (MSA) is a rare neurodegenerative disease, with limited understanding of disease progression and prognostic factors. We leveraged the…”
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    Journal Article
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    Multiple System Atrophy: Recent Developments and Future Perspectives by Meissner, Wassilios G., Fernagut, Pierre‐Olivier, Dehay, Benjamin, Péran, Patrice, Traon, Anne Pavy‐Le, Foubert‐Samier, Alexandra, Lopez Cuina, Miguel, Bezard, Erwan, Tison, François, Rascol, Olivier

    Published in Movement disorders (01-11-2019)
    “…Multiple system atrophy (MSA) is a rare and fatal neurodegenerative disorder characterized by a variable combination of parkinsonism, cerebellar impairment,…”
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    Trends in Prevalence of Dementia in French Farmers from Two Epidemiological Cohorts by Pérès, Karine, Brayne, Carol, Matharan, Fanny, Grasset, Leslie, Helmer, Catherine, Letenneur, Luc, Foubert‐Samier, Alexandra, Baldi, Isabelle, Tison, François, Amieva, Hélène, Dartigues, Jean‐François

    “…Objectives To determine the prevalence of dementia and cognitive impairment in older people across generations. Design Two prospective cohort studies…”
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    Journal Article
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    Characterization of Recessive Parkinson Disease in a Large Multicenter Study by Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Romdhan, Sawssan Ben, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Toullec, Benjamin Le, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohamed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Ben Romdhan, Sawssan, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Le Toullec, Benjamin, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Ben Djebara, Mouna, Gouider, Riadh, Tazir, Meriem, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andy, Corvol, Jean‐Christophe, Brice, Alexis

    Published in Annals of neurology (01-10-2020)
    “…Studies of the phenotype and population distribution of rare genetic forms of parkinsonism are required, now that gene‐targeting approaches for Parkinson…”
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    Journal Article
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    Genome sequence analyses identify novel risk loci for multiple system atrophy by Chia, Ruth, Ray, Anindita, Shah, Zalak, Ding, Jinhui, Ruffo, Paola, Fujita, Masashi, Menon, Vilas, Saez-Atienzar, Sara, Reho, Paolo, Kaivola, Karri, Walton, Ronald L, Reynolds, Regina H, Karra, Ramita, Sait, Shaimaa, Akcimen, Fulya, Diez-Fairen, Monica, Alvarez, Ignacio, Fanciulli, Alessandra, Stefanova, Nadia, Seppi, Klaus, Duerr, Susanne, Leys, Fabian, Krismer, Florian, Sidoroff, Victoria, Zimprich, Alexander, Pirker, Walter, Rascol, Olivier, Foubert-Samier, Alexandra, Meissner, Wassilios G, Tison, François, Pavy-Le Traon, Anne, Pellecchia, Maria Teresa, Barone, Paolo, Russillo, Maria Claudia, Marín-Lahoz, Juan, Kulisevsky, Jaime, Torres, Soraya, Mir, Pablo, Periñán, Maria Teresa, Proukakis, Christos, Chelban, Viorica, Wu, Lesley, Goh, Yee Y, Parkkinen, Laura, Hu, Michele T, Kobylecki, Christopher, Saxon, Jennifer A, Rollinson, Sara, Garland, Emily, Biaggioni, Italo, Litvan, Irene, Rubio, Ileana, Alcalay, Roy N, Kwei, Kimberly T, Lubbe, Steven J, Mao, Qinwen, Flanagan, Margaret E, Castellani, Rudolph J, Khurana, Vikram, Ndayisaba, Alain, Calvo, Andrea, Mora, Gabriele, Canosa, Antonio, Floris, Gianluca, Bohannan, Ryan C, Moore, Anni, Norcliffe-Kaufmann, Lucy, Palma, Jose-Alberto, Kaufmann, Horacio, Kim, Changyoun, Iba, Michiyo, Masliah, Eliezer, Dawson, Ted M, Rosenthal, Liana S, Pantelyat, Alexander, Albert, Marilyn S, Pletnikova, Olga, Troncoso, Juan C, Infante, Jon, Lage, Carmen, Sánchez-Juan, Pascual, Serrano, Geidy E, Beach, Thomas G, Pastor, Pau, Morris, Huw R, Albani, Diego, Clarimon, Jordi, Wenning, Gregor K, Hardy, John A, Ryten, Mina, Topol, Eric, Torkamani, Ali, Chiò, Adriano, Bennett, David A, De Jager, Philip L, Low, Philip A, Singer, Wolfgang, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W

    Published in Neuron (Cambridge, Mass.) (03-07-2024)
    “…Multiple system atrophy (MSA) is an adult-onset, sporadic synucleinopathy characterized by parkinsonism, cerebellar ataxia, and dysautonomia. The genetic…”
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    Journal Article
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