Found: 6

Select item for more details and to access through your institution.

  • Choreic syndrome due to Hashimoto's encephalopathy.

    Published in:
    Movement Disorders, 2002, v. 17, n. 5, p. 1091, doi. 10.1002/mds.10230
    By:
    • Taurin, Gregory;
    • Golfier, Véronique;
    • Pinel, Jean-François;
    • Deburghgraeve, Véronique;
    • Poirier, Jean-Yves;
    • Edan, Gilles;
    • Vérin, Marc
    Publication type:
    Article

  • Memantine in Behavioral Variant Frontotemporal Dementia: Negative Results.

    Published in:
    Journal of Alzheimer's Disease, 2011, v. 23, n. 4, p. 749, doi. 10.3233/JAD-2010-101632
    By:
    • Vercelletto, Martine;
    • Boutoleau-Bretonnière, Claire;
    • Volteau, Christelle;
    • Puel, Michèle;
    • Auriacombe, Sophie;
    • Sarazin, Marie;
    • Michel, Bernard-François;
    • Couratier, Philippe;
    • Thomas-Antérion, Catherine;
    • Verpillat, Patrice;
    • Gabelle, Audrey;
    • Golfier, Véronique;
    • Cerato, Evelyne;
    • Lacomblez, Lucette
    Publication type:
    Article

  • FUS Mutations in Frontotemporal Lobar Degeneration with Amyotrophic Lateral Sclerosis.

    Published in:
    Journal of Alzheimer's Disease, 2010, v. 22, n. 3, p. 765, doi. 10.3233/JAD2010100837
    By:
    • Broustal, Oriane;
    • Camuzat, Agnès;
    • Guillot-Noël, Lena;
    • Guy, Nathalie;
    • Millecamps, Stéphanie;
    • Deffond, Didier;
    • Lacomblez, Lucette;
    • Golfier, Véronique;
    • Hannequin, Didier;
    • Salachas, François;
    • Camu, William;
    • Didic, Mira;
    • Dubois, Bruno;
    • Meininger, Vincent;
    • Le Ber, Isabelle;
    • Brice, Alexis
    Publication type:
    Article

  • Progranulin null mutations in both sporadic and familial frontotemporal dementia.

    Published in:
    Human Mutation, 2007, v. 28, n. 9, p. 846, doi. 10.1002/humu.20520
    By:
    • Le Ber, Isabelle;
    • van der Zee, Julie;
    • Hannequin, Didier;
    • Gijselinck, Ilse;
    • Campion, Dominique;
    • Puel, Michèle;
    • Laquerrière, Annie;
    • De Pooter, Tim;
    • Camuzat, Agnès;
    • Van den Broeck, Marleen;
    • Dubois, Bruno;
    • Sellal, François;
    • Lacomblez, Lucette;
    • Vercelletto, Martine;
    • Thomas-Antérion, Catherine;
    • Michel, Bernard-François;
    • Golfier, Véronique;
    • Didic, Mira;
    • Salachas, François;
    • Duyckaerts, Charles
    Publication type:
    Article

  • TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration.

    Published in:
    Annals of Neurology, 2009, v. 65, n. 4, p. 470, doi. 10.1002/ana.21612
    By:
    • Benajiba, Lina;
    • Le Ber, Isabelle;
    • Camuzat, Agnès;
    • Lacoste, Mathieu;
    • Thomas-Anterion, Catherine;
    • Couratier, Philippe;
    • Legallic, Solenn;
    • Salachas, François;
    • Hannequin, Didier;
    • Decousus, Marielle;
    • Lacomblez, Lucette;
    • Guedj, Eric;
    • Golfier, Véronique;
    • Camu, William;
    • Dubois, Bruno;
    • Campion, Dominique;
    • Meininger, Vincent;
    • Brice, Alexis
    Publication type:
    Article

  • Genetic Analysis of Inherited Leukodystrophies Genotype-Phenotype Correlations in the CSF1R Gene.

    Published in:
    JAMA Neurology, 2013, v. 70, n. 7, p. 875, doi. 10.1001/jamaneurol.2013.698
    By:
    • Guerreiro, Rita;
    • Kara, Eleanna;
    • Le Ber, Isabelle;
    • Bras, Jose;
    • Rohrer, Jonathan D.;
    • Taipa, Ricardo;
    • Lashley, Tammaryn;
    • Dupuits, Céline;
    • Gurunlian, Nicole;
    • Mochel, Fanny;
    • Warren, Jason D.;
    • Hannequin, Didier;
    • Sedel, Frédéric;
    • Depienne, Christel;
    • Camuzat, Agnès;
    • Golfier, Véronique;
    • Du Boisguéheneuc, Foucaud;
    • Schottlaender, Lucia;
    • Fox, Nick C.;
    • Beck, Jonathan
    Publication type:
    Article