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Showing articles 0 to 3 of 3 Filter Applied: Parkinson disease,familial (Click to remove) The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2 Arch Neurol 61:35-38, Lu,C.,et al, 2004 Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease Lancet 365:410-412, Nichols, W.C., et al, 2005 Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism Neurol 35:227-234, Jankovic,J.,et al, 1985 Showing articles 0 to 3 of 3