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Plos One|August 15, 2009
Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathyMargot Fournier, Jérémie Vitte, Jérôme Garrigue, et al.
Journal of Neuroinflammation|May 26, 2016
Inflammatory profile in LRRK2-associated prodromal and clinical PDKathrin Brockmann, Anja Apel, Claudia Schulte, et al.
Brain : a Journal of Neurology|November 9, 2022
Association between the LRP1B and APOE loci and the development of Parkinson's disease dementiaRaquel Real, Alejandro Martinez-Carrasco, Regina H Reynolds, et al.
Neurology. Genetics|March 27, 2018
ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegiaChristian G Bouwkamp, Zaid Afawi, Aviva Fattal-Valevski, et al.
Archives of Neurology|March 14, 2007
LRRK2 exon 41 mutations in sporadic Parkinson disease in EuropeansSuzanne Lesage, Sabine Janin, Ebba Lohmann, et al.
Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2019
Examining the Reserve Hypothesis in Parkinson's Disease: A Longitudinal StudyPei-Chen Lee, Fanny Artaud, Florence Cormier-Dequaire, et al.
Journal of the Neurological Sciences|December 17, 2008
Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: further mutations and relative frequency in ZFYVE26/SPG15 in the Italian populationPaola S Denora, Maria Muglia, Carlo Casali, et al.
Neurology|June 22, 2018
Longitudinal analysis of impulse control disorders in Parkinson diseaseJean-Christophe Corvol, Fanny Artaud, Florence Cormier-Dequaire, et al.
Human Molecular Genetics|March 19, 2026
Association of rare apolipoprotein E ε4 homozygosity with an earlier age at onset in spinocerebellar ataxia type 3Charlotte Clara Meyer, Eduardo Preusser de Mattos, Rahel Maria Burger, et al.
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