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Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

artículo científico publicado en 2004

Analysis of the glucocerebrosidase gene in Parkinson's disease

article

Childhood Onset in Familial Prion Disease With a Novel Mutation in the PRNP Gene

article

Clinical findings in a large family with a parkin ex3delta40 mutation

artículo científico publicado en 2004

Genetic Variability in CHMP2B and Frontotemporal Dementia

article

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

artículo científico publicado en 2004

Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients

scholarly article by Cindy Zadikoff et al published 17 March 2006 in Movement Disorders

NovelSPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia

Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations

artículo científico publicado en 2005

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