Výsledky vyhledávání - Vincent Huin

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  1. 1
    Cognitive Impairment Is Part of the Phenotype of Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (<scp>CANVAS)</scp>

    Cognitive Impairment Is Part of the Phenotype of Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (<scp>CANVAS)</scp> Autor Kathy Dujardin, Céline Tard, Emily Diglé, Virginie Herlin, Eugénie Mutez, Jean‐Baptiste Davion, Anna Wissocq, Violette Delforge, Grégory Kuchcinski, Vincent Huin

    Vydáno 2024
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  2. 2
    Comparing high and low amyloid producers in Alzheimer's disease: An in-depth analysis

    Comparing high and low amyloid producers in Alzheimer's disease: An in-depth analysis Autor Mélanie Leroy, Anne Laure Aziz, Susanna Schraen, Vincent Deramecourt, Emilie Skrobala, Simon Lecerf, Florence Pasquier, Vincent Huin, Maxime Bertoux, Thibaud Lebouvier

    Vydáno 2025
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  3. 3
    A geographical cluster of progressive supranuclear palsy in northern France

    A geographical cluster of progressive supranuclear palsy in northern France Autor D Caparros-Lefèbvre, Lawrence I. Golbe, Vincent Deramecourt, Claude‐Alain Maurage, Vincent Huin, Valérie Buée‐Scherrer, Hélène Obriot, Bernard Sablonnière, François Caparros, Luc Buée, Andrew J. Lees

    Vydáno 2015
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  4. 4
    TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment

    TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment Autor Jérôme Delplanque, David Devos, Vincent Huin, Alexandre Genet, Olivier Sand, Caroline Moreau, Cyril Goizet, Perrine Charles, Mathieu Anheim, Marie Lorraine Monin, Luc Buée, A. Destée, Guillaume Grolez, Christine Delmaire, Kathy Dujardin, Delphine Dellacherie, Alexis Brice, Giovanni Stévanin, Isabelle Strubi-Vuillaume, Alexandra Dürr, Bernard Sablonnière

    Vydáno 2014
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  5. 5
    Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms

    Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms Autor Vincent Huin, Mathieu Barbier, Armand Bottani, Johannes Alexander Lobrinus, Fabienne Clot, Foudil Lamari, Laureen Chat, Benoît Rucheton, Frédérique Fluchère, Stéphane Auvin, Peter L. Myers, A. Gélot, Agnès Camuzat, Catherine Caillaud, Ludmila Jornéa, Sylvie Forlani, Dario Saracino, Charles Duyckaerts, Alexis Brice, Alexandra Dürr, Isabelle Le Ber

    Vydáno 2019
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  6. 6
    P2X7-deficiency improves plasticity and cognitive abilities in a mouse model of Tauopathy

    P2X7-deficiency improves plasticity and cognitive abilities in a mouse model of Tauopathy Autor Kévin Carvalho, Elodie Martin, Aurélia Cès, Nadège Sarrazin, Pauline Lagouge-Roussey, Caroline Nous, Leyna Boucherit, Ihsen Youssef, Annick Prigent, Émilie Faivre, Sabiha Eddarkaoui, Thibaut Gauvrit, Didier Vieau, Susana Boluda, Vincent Huin, Bertrand Fontaine, Luc Buée, Benoı̂t Delatour, P. Dutar, Florian Sennlaub, Xavier Guillonneau, David Blum, Cécile Delarasse

    Vydáno 2021
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  7. 7
    Motor neuron pathology in CANVAS due to <i>RFC1</i> expansions

    Motor neuron pathology in CANVAS due to <i>RFC1</i> expansions Autor Vincent Huin, Giulia Coarelli, Clément Guemy, Susana Boluda, Rabab Debs, Fanny Mochel, Tanya Stojkovic, David Grabli, Thierry Maisonobe, Bertrand Gaymard, Timothée Lenglet, Céline Tard, Jean Baptiste Davion, Bernard Sablonnière, Marie Lorraine Monin, Claire Ewenczyk, Karine Viala, Perrine Charles, Isabelle Le Ber, Mary M Reilly, Henry Houlden, Andrea Cortese, Danielle Seilhean, Alexis Brice, Alexandra Dürr

    Vydáno 2021
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  8. 8
    Exacerbation of C1q dysregulation, synaptic loss and memory deficits in tau pathology linked to neuronal adenosine A2A receptor

    Exacerbation of C1q dysregulation, synaptic loss and memory deficits in tau pathology linked to neuronal adenosine A2A receptor Autor Kévin Carvalho, Émilie Faivre, Marie J. Pietrowski, Xavier Marques, Victoria Gómez‐Murcia, Aude Deleau, Vincent Huin, Jan N. Hansen, Stanislav Kozlov, Clément Danis, Mariana Temido‐Ferreira, Joana E. Coelho, Céline Mériaux, Sabiha Eddarkaoui, Stéphanie Le Gras, Mélanie Dumoulin, Lucrezia Cellai, Isabelle Landrieu, Y. F. Chern, Malika Hamdane, Luc Buée, Anne‐Laurence Boutillier, Sabine Lévi, Annett Halle, Luı́sa V. Lopes, David Blum

    Vydáno 2019
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  9. 9
    Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia

    Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia Autor 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

    Vydáno 2021
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  10. 10
    Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease

    Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease Autor Riccardo Currò, Natalia Dominik, Stefano Facchini, Elisa Vegezzi, Roisin Sullivan, Valentina Galassi Deforie, Gorka Fernández‐Eulate, Andreas Traschütz, Salvatore Rossi, Matteo Garibaldi, Mariusz Kwarciany, Franco Taroni, Alfredo Brusco, Jean-Marc Good, Francesca Cavalcanti, Simon Hammans, Gianina Ravenscroft, Richard Roxburgh, Inés Albájar, Catherine Ashton, Nick Beauchamp, Sarah J. Beecroft, Emilia Bellone, José Berciano, Petya Bogdanova‐Mihaylova, Barbara Borroni, Bernard Brais, Enrico Bugiardini, Catarina Falcão de Campos, Aisling Carr, Liam Carroll, Francesca Castellani, Tiziana Cavallaro, Patrick F. Chinnery, Silvia Colnaghi, Giuseppe Cosentino, Joana Damásio, Soma Das, Grazia Devigili, Daniela Di Bella, D J Dick, Alexandra Dürr, Amar El-Saddig, Jennifer Faber, Moreno Ferrarini, Massimiliano Filosto, Geraint Fuller, Salvatore Gallone, Chiara Gemelli, Marina Grandis, John Hardy, Channa Hewamadduma, Rita Horváth, Vincent Huin, Daniele Imperiale, Pablo Iruzubieta, Diego Kaski, Andrew King, Thomas Klockgether, Müge Kovancılar Koç, Kishore R. Kumar, Thierry Küntzer, Nigel G. Laing, Matilde Laurá, Timothy Lavin, Peter Leigh, Lea Leonardis, Michael P. Lunn, Stefania Magri, Francesca Magrinelli, Maria João Malaquias, Michelangelo Mancuso, Hadi Manji, Sara Massucco, John McConville, Renato P. Munhoz, Sara Nagy, Alain Ndayisaba, Andrea H. Németh, Luiz Eduardo Novis, Johanna Palmio, Elena Pegoraro, David Pellerin, Benedetta Perrone, Chiara Pisciotta, James M. Polke, Malcolm J. Proudfoot, Laura Orsi, Aleksandar Radunović, Nilo Riva, Aiko Robert, Riccardo Ronco, Elena Rossini, Alexander M. Rossor, Irmak Şahbaz, Qais Sa’di, Ettore Salsano, Alessandro Salvalaggio, Lucio Santoro, Elisa Sarto

    Vydáno 2024
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