Export 184 results:
Filters: Author is Leveille, Etienne [Clear All Filters]
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Mol Genet Genomic Med. 2020;:e1052..
The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal Biorepository. J Parkinsons Dis. 2020;10(1):301-313..
Association study of essential tremor genetic loci in Parkinson's disease. Neurobiol Aging. 2018;66:178.e13-178.e15..
Sequencing of the GBA coactivator, Saposin C, in Parkinson disease. Neurobiol Aging. 2018;..