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Neurology|January 21, 2009
Autosomal dominant subcortical gliosis presenting as frontotemporal dementiaR H Swerdlow, B B Miller, M B S Lopes, et al.Neurology|March 15, 2006
Optimizing the ongoing search for new treatments for Parkinson disease: using futility designsB C Tilley, Y Y Palesch, K Kieburtz, et al.Journal of Neurochemistry|September 15, 2000
Mitochondrial dysfunction in cybrid lines expressing mitochondrial genes from patients with progressive supranuclear palsyR H Swerdlow, L I Golbe, J K Parks, et al.American Journal of Medical Genetics|April 27, 2002
Segregation analysis of Parkinson disease revealing evidence for a major causative geneN E Maher, L J Currie, A M Lazzarini, et al.Neurology|January 15, 2003
Randomized, double-blind trial of glial cell line-derived neurotrophic factor (GDNF) in PDJ G Nutt, K J Burchiel, C L Comella, et al.Annals of Neurology|December 16, 1998
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease familyR H Swerdlow, J K Parks, J N Davis, et al.Neurology|January 10, 2002
Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD studyN E Maher, L I Golbe, A M Lazzarini, et al.Neurology|September 26, 2001
Genome-wide scan for Parkinson's disease: the GenePD StudyA L DeStefano, L I Golbe, M H Mark, et al.Neurology|December 10, 2003
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD studyS Karamohamed, A L DeStefano, J B Wilk, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2005
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD studySamer Karamohamed, L I Golbe, M H Mark, et al.Pageof 9