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Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis 2009
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Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; ... Brice, Alexis 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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SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia Marelli, Cecilia; van de Leemput, Joyce; Johnson, Janel O; Tison, Francois; ... Brice, Alexis 2011
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Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease Lesage, Suzanne; Anheim, Mathieu; Condroyer, Christel; Pollak, Pierre; ... Brice, Alexis 2011
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PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population Méneret, Aurélie; Grabli, David; Depienne, Christel; Gaudebout, Cécile; ... Roze, Emmanuel 2012