检索结果 - Agnès Camuzat

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  1. 1
    Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy‐like tauopathy

    Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy‐like tauopathy 由 D Caparros-Lefèbvre, Nicolas Sergeant, Andrew J. Lees, Agnès Camuzat, Susan E. Daniel, Annie Lannuzel, Alexis Brice, Eduardo Tolosa, André Delacourte, Charles Duyckaerts

    出版 2002
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  2. 2
    Mapping of Spinocerebellar Ataxia 13 to Chromosome 19q13.3-q13.4 in a Family with Autosomal Dominant Cerebellar Ataxia and Mental Retardation

    Mapping of Spinocerebellar Ataxia 13 to Chromosome 19q13.3-q13.4 in a Family with Autosomal Dominant Cerebellar Ataxia and Mental Retardation 由 Alexandra Herman-Bert, Giovanni Stévanin, J C Netter, Olivier Rascol, David Brassat, Patrick Calvas, Agnès Camuzat, Qiuping Yuan, Martin Schalling, Alexandra Dürr, Alexis Brice

    出版 2000
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  3. 3
    Homozygous TREM2 mutation in a family with atypical frontotemporal dementia

    Homozygous TREM2 mutation in a family with atypical frontotemporal dementia 由 Isabelle Le Ber, Anne de Septenville, Rita Guerreiro, José Brás, Agnès Camuzat, Paola Caroppo, Serena Lattante, Philippe Couarch, Edor Kabashi, Kawtar Bouya-Ahmed, Bruno Dubois, Alexis Brice

    出版 2014
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  4. 4
    Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis

    Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis 由 Patrice Verpillat, Agnès Camuzat, Didier Hannequin, Catherine Thomas-Antérion, Michèle Puel, Serge Belliard, Bruno Dubois, Mira Didic, Lucette Lacomblez, Olivier Moreaud, Véronique Golfier, Dominique Campion, Alexis Brice, Françoise Clerget‐Darpoux

    出版 2002
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  5. 5
    <i>DCTN1</i>Mutation Analysis in Families With Progressive Supranuclear Palsy–Like Phenotypes

    <i>DCTN1</i>Mutation Analysis in Families With Progressive Supranuclear Palsy–Like Phenotypes 由 Paola Caroppo, Isabelle Le Ber, Fabienne Clot, Sophie Rivaud-Péchoux, Agnès Camuzat, Anne de Septenville, Claire Boutoleau‐Bretonnière, Vanessa Mourlon, Mathilde Sauvée, Thibaud Lebouvier, Anne-Marie Bonnet, Richard Lévy, Martine Vercelletto, Alexis Brice

    出版 2014
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  6. 6
    Association Between the Extended tau Haplotype and Frontotemporal Dementia

    Association Between the Extended tau Haplotype and Frontotemporal Dementia 由 Patrice Verpillat, Agnès Camuzat, Didier Hannequin, Catherine Thomas-Antérion, Michèle Puel, Serge Belliard, Bruno Dubois, Mira Didic, Bernard‐François Michel, Lucette Lacomblez, Olivier Moreaud, François Sellal, Véronique Golfier, Dominique Campion, Françoise Clerget‐Darpoux, Alexis Brice

    出版 2002
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  7. 7
    Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy

    Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy 由 Ammar Al‐Chalabi, Alexandra Dürr, Nicholas Wood, Michael Parkinson, Agnès Camuzat, Jean‐Sébastien Hulot, Karen Morrison, Alan E. Renton, Sigurd D. Sussmuth, G. Bernhard Landwehrmeyer, Albert Ludolph, Y. Agid, Alexis Brice, P. Nigel Leigh, Gilbert Bensimon

    出版 2009
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  8. 8
    <i>SQSTM1</i>Mutations in French Patients With Frontotemporal Dementia or Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

    <i>SQSTM1</i>Mutations in French Patients With Frontotemporal Dementia or Frontotemporal Dementia With Amyotrophic Lateral Sclerosis 由 Isabelle Le Ber, Agnès Camuzat, Rita Guerreiro, Kawtar Bouya-Ahmed, José Brás, Gaël Nicolas, Audrey Gabelle, Mira Didic, Anne de Septenville, Stéphanie Millecamps, Timothée Lenglet, Morwena Latouche, Edor Kabashi, Dominique Campion, Didier Hannequin, John Hardy, Alexis Brice

    出版 2013
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  9. 9
    Presymptomatic spinal cord pathology in <i>c9orf72</i> mutation carriers: A longitudinal neuroimaging study

    Presymptomatic spinal cord pathology in <i>c9orf72</i> mutation carriers: A longitudinal neuroimaging study 由 Giorgia Querin, Peter Bede, Mohamed Mounir El Mendili, Menghan Li, Mélanie Pélégrini‐Issac, Daisy Rinaldi, Martin Catala, Dario Saracino, François Salachas, Agnès Camuzat, Véronique Marchand‐Pauvert, Julien Cohen‐Adad, Olivier Colliot, Isabelle Le Ber, Pierre‐François Pradat

    出版 2019
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  10. 10
    Plasma microRNA signature in presymptomatic and symptomatic subjects with <i>C9orf72</i>-associated frontotemporal dementia and amyotrophic lateral sclerosis

    Plasma microRNA signature in presymptomatic and symptomatic subjects with <i>C9orf72</i>-associated frontotemporal dementia and amyotrophic lateral sclerosis 由 Virgilio Kmetzsch, Vincent Anquetil, Dario Saracino, Daisy Rinaldi, Agnès Camuzat, Thomas Gareau, Ludmila Jornéa, Sylvie Forlani, Philippe Couratier, David Wallon, Florence Pasquier, Noémie Robil, Pierre de la Grange, Ivan Moszer, Isabelle Le Ber, Olivier Colliot, E. Becker

    出版 2020
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  11. 11
    Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

    Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum 由 Dominique Campion, Cécile Dumanchin, Didier Hannequin, Bruno Dubois, Serge Belliard, Michèle Puel, Catherine Thomas-Antérion, Agnès Michon, Cosette Martin, Françoise Charbonnier, Grégory Raux, Agnès Camuzat, Christiane Penet, Valérie Mesnage, María Martínez, Françoise Clerget‐Darpoux, Alexis Brice, Thierry Frébourg

    出版 1999
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  12. 12
    Defining the spectrum of frontotemporal dementias associated with <i>TARDBP</i> mutations

    Defining the spectrum of frontotemporal dementias associated with <i>TARDBP</i> mutations 由 Paola Caroppo, Agnès Camuzat, Léna Guillot‐Noël, Catherine Thomas-Antérion, Philippe Couratier, Tsz Hang Wong, Marc Teichmann, Véronique Golfier, Sophie Auriacombe, Serge Belliard, Bernard Laurent, Serena Lattante, Stéphanie Millecamps, Fabienne Clot, Bruno Dubois, John C. van Swieten, Alexis Brice, Isabelle Le Ber

    出版 2016
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  13. 13
    Early Cognitive, Structural, and Microstructural Changes in Presymptomatic <i>C9orf72</i> Carriers Younger Than 40 Years

    Early Cognitive, Structural, and Microstructural Changes in Presymptomatic <i>C9orf72</i> Carriers Younger Than 40 Years 由 Anne Bertrand, Junhao Wen, Daisy Rinaldi, Marion Houot, Sabrina Sayah, Agnès Camuzat, Clémence Fournier, Sabrina Fontanella, Alexandre Routier, Philippe Couratier, Florence Pasquier, Marie‐Odile Habert, Didier Hannequin, Olivier Martinaud, Paola Caroppo, Richard Lévy, Bruno Dubois, Alexis Brice, Stanley Durrleman, Olivier Colliot, Isabelle Le Ber

    出版 2018
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  14. 14
    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 由 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

    出版 2019
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  15. 15
    Contribution of <i>ATXN2</i> intermediary polyQ expansions in a spectrum of neurodegenerative disorders

    Contribution of <i>ATXN2</i> intermediary polyQ expansions in a spectrum of neurodegenerative disorders 由 Serena Lattante, Stéphanie Millecamps, Giovanni Stévanin, Sophie Rivaud-Péchoux, Carine Moigneu, Agnès Camuzat, Sandra da Barroca, Emeline Mundwiller, Philippe Couarch, François Salachas, Didier Hannequin, Vincent Meininger, Florence Pasquier, Danielle Seilhean, Philippe Couratier, Véronique Danel-Brunaud, Muriel Bonnet, Christine Tranchant, Eric LeGuern, Alexis Brice, Isabelle Le Ber, Edor Kabashi

    出版 2014
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  16. 16
    Genetic Analysis of Inherited Leukodystrophies

    Genetic Analysis of Inherited Leukodystrophies 由 Rita Guerreiro, Eleanna Kara, Isabelle Le Ber, José Brás, Jonathan D. Rohrer, Ricardo Taipa, Tammaryn Lashley, Céline Dupuits, Nicole Gurunlian, Fanny Mochel, Jason D. Warren, Didier Hannequin, Frédéric Sedel, Christel Depienne, Agnès Camuzat, Véronique Golfier, Foucaud Du Boisguéheneuc, Lucía Schottlaender, Nick C. Fox, Jonathan Beck, Simon Mead, Martin N. Rossor, John Hardy, Tamás Révész, Alexis Brice, Henry Houlden

    出版 2013
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  17. 17
    Progranulin null mutations in both sporadic and familial frontotemporal dementia

    Progranulin null mutations in both sporadic and familial frontotemporal dementia 由 Isabelle Le Ber, Julie van der Zee, Didier Hannequin, Ilse Gijselinck, Dominique Campion, Michèle Puel, Annie Laquerrière, Tim De Pooter, Agnès Camuzat, Marleen Van den Broeck, Bruno Dubois, François Sellal, Lucette Lacomblez, Martine Vercelletto, Catherine Thomas-Antérion, Bernard‐François Michel, Véronique Golfier, Mira Didic, François Salachas, Charles Duyckaerts, Marc Cruts, Patrice Verpillat, Christine Van Broeckhoven, Alexis Brice

    出版 2007
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  18. 18
    Plasma NfL levels and longitudinal change rates in <i>C9orf72</i> and <i>GRN</i>-associated diseases: from tailored references to clinical applications

    Plasma NfL levels and longitudinal change rates in <i>C9orf72</i> and <i>GRN</i>-associated diseases: from tailored references to clinical applications 由 Dario Saracino, Karim Dorgham, Agnès Camuzat, Daisy Rinaldi, Armelle Rametti‐Lacroux, Marion Houot, Fabienne Clot, Philippe Martin-Hardy, Ludmila Jornéa, Carole Azuar, Raffaella Migliaccio, Florence Pasquier, Philippe Couratier, Sophie Auriacombe, Mathilde Sauvée, Claire Boutoleau‐Bretonnière, Jérémie Pariente, Mira Didic, Didier Hannequin, David Wallon, Olivier Colliot, Bruno Dubois, Alexis Brice, Richard Lévy, Sylvie Forlani, Isabelle Le Ber

    出版 2021
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  19. 19
    Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia

    Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia 由 Julie van der Zee, Isabelle Le Ber, Sebastian Maurer‐Stroh, Sebastiaan Engelborghs, Ilse Gijselinck, Agnès Camuzat, Nathalie Brouwers, Rik Vandenberghe, Kristel Sleegers, Didier Hannequin, Bart Dermaut, Joost Schymkowitz, Dominique Campion, Patrick Santens, Jean‐Jacques Martin, Lucette Lacomblez, Tim De Pooter, Karin Peeters, Maria Mattheijssens, Martine Vercelletto, Marleen Van den Broeck, Marc Cruts, Peter Paul De Deyn, Frédéric Rousseau, Alexis Brice, Christine Van Broeckhoven

    出版 2007
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  20. 20
    Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experience

    Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experience 由 Leila Sellami, Benoît Rucheton, Imen Ben Younes, Agnès Camuzat, Dario Saracino, Daisy Rinaldi, Stéphane Epelbaum, Carole Azuar, Richard Lévy, Sophie Auriacombe, Didier Hannequin, Jérémie Pariente, Mathieu Barbier, Claire Boutoleau‐Bretonnière, Philippe Couratier, Florence Pasquier, Vincent Deramecourt, Mathilde Sauvée, Marie Sarazin, Julien Lagarde, Carole Roué-Jagot, Sylvie Forlani, Ludmila Jornéa, I. Rodenhiser David, Eric LeGuern, Bruno Dubois, Alexis Brice, Fabienne Clot, Foudil Lamari, Isabelle Le Ber

    出版 2020
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