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Neuropsychologia|December 25, 2012
Is non-recognition of choreic movements in Huntington disease always pathological?Damian Justo, Perrine Charles, Jean Daunizeau, et al.European Journal of Human Genetics : EJHG|October 25, 2007
Mental deficiency in three families with SPG4 spastic paraplegiaPascale Ribaï, Christel Depienne, Estelle Fedirko, et al.Archives of Neurology|June 15, 2007
Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patientsPascale Ribaï, Karine Nguyen, Valérie Hahn-Barma, et al.Journal of Inherited Metabolic Disease|November 13, 2014
Cognitive profile of patients with glycogen storage disease type III: a clinical description of seven casesClaire-Cécile Michon, Marcela Gargiulo, Valérie Hahn-Barma, et al.Brain : a Journal of Neurology|June 28, 2011
Similar amyloid-β burden in posterior cortical atrophy and Alzheimer's diseaseLeonardo Cruz de Souza, Fabian Corlier, Marie-Odile Habert, et al.The Lancet. Neurology|February 17, 2007
Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up studyMarie Vidailhet, Laurent Vercueil, Jean-Luc Houeto, et al.Brain : a Journal of Neurology|February 5, 2008
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic studyIsabelle Le Ber, Agnès Camuzat, Didier Hannequin, et al.Pageof 1