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Human Molecular Genetics|September 16, 1998
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonismC Dumanchin, A Camuzat, D Campion, et al.The New England Journal of Medicine|May 29, 2000
Association between early-onset Parkinson's disease and mutations in the parkin geneC B Lücking, A Dürr, V Bonifati, et al.Neurology|November 7, 2008
A multidisciplinary study of patients with early-onset PD with and without parkin mutationsE Lohmann, S Thobois, S Lesage, et al.Neurology|July 1, 1996
Consequence of nigrostriatal denervation and L-dopa therapy on the expression of glutamic acid decarboxylase messenger RNA in the pallidumM T Herrero, R Levy, M Ruberg, et al.Journal of Medical Genetics|August 1, 1996
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study GroupD Campion, A Brice, D Hannequin, et al.Neurology|March 1, 1996
Consequences of nigrostriatal denervation on the gamma-aminobutyric acidic neurons of substantia nigra pars reticulata and superior colliculus in parkinsonian syndromesM Vila, M T Herrero, R Levy, et al.Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 2, 2001
Idazoxan, an alpha-2 antagonist, and L-DOPA-induced dyskinesias in patients with Parkinson's diseaseO Rascol, I Arnulf, H Peyro-Saint Paul, et al.Annals of Neurology|December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brainI Gourfinkel-An, G Cancel, Y Trottier, et al.Pageof 56