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 TitleAuthors / EditorsDate
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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe 2013
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EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis 2012
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Screening of the THAP1 gene in patients with early-onset dystonia: myoclonic jerks are part of the dystonia 6 phenotype Clot, Fabienne; Grabli, David; Burbaud, Pierre; Aya, Magali; ... Brice, Alexis 2011
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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Saad, Mohamad; Lesage, Suzanne; Saint-Pierre, Aude; Corvol, Jean-Christophe; ... Brice, Alexis 2011
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Repetitive behaviours in patients with Gilles de la Tourette syndrome: tics, compulsions, or both? Worbe, Yulia; Mallet, Luc; Golmard, Jean-Louis; Béhar, Cécile; ... Hartmann, Andreas 2010
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Follow-up study of the GIGYF2 gene in French families with Parkinson's disease Lesage, Suzanne; Condroyer, Christel; Lohman, Ebba; Troiano, André; ... Brice, Alexis 2010
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In vivo evidence for the selective subcortical degeneration in Huntington's disease Douaud, Gwenaëlle; Behrens, Timothy E.; Poupon, Cyril; Cointepas, Yann; ... Remy, Philippe 2009
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Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia Clot, Fabienne; Grabli, David; Cazeneuve, Cecile; Roze, Emmanuel; ... Brice, Alexis 2009
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Neuropsychological changes between "off" and "on" STN or GPi stimulation in Parkinson's disease Pilln, Bernard; Ardouin, Claire; Damier, Philippe; Krack, Paul; ... Agid, Yves 2000