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Neurology|September 17, 2017
Analysis of blood-based gene expression in idiopathic Parkinson diseaseRon Shamir, Christine Klein, David Amar, et al.
Archives of Neurology|September 13, 2006
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutationsLianna Ishihara, Liling Warren, Rachel Gibson, et al.
Brain : a Journal of Neurology|January 4, 2022
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegiaJean-Loup Méreaux, Guillaume Banneau, Mélanie Papin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2022
The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4Livia Parodi, Mathieu Barbier, Maxime Jacoupy, et al.
The Lancet. Neurology|January 22, 2022
Safety and efficacy of riluzole in spinocerebellar ataxia type 2 in France (ATRIL): a multicentre, randomised, double-blind, placebo-controlled trialGiulia Coarelli, Anna Heinzmann, Claire Ewenczyk, et al.
Biological Psychiatry|March 13, 2009
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disordersChristel Depienne, Daniel Moreno-De-Luca, Delphine Heron, et al.
Plos One|September 23, 2016
COMT Val158Met Polymorphism Modulates Huntington's Disease ProgressionRuth de Diego-Balaguer, Catherine Schramm, Isabelle Rebeix, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutationsStephan Klebe, Alexander Lossos, Hamid Azzedine, et al.
Science (New York, N.Y.)|November 26, 2002
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismVincenzo Bonifati, Patrizia Rizzu, Marijke J van Baren, et al.
Neurology|August 8, 2014
Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disordersSerena Lattante, Stéphanie Millecamps, Giovanni Stevanin, et al.
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