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Neurobiology of Disease|February 26, 2021
Plasma neurofilament light chain predicts cerebellar atrophy and clinical progression in spinocerebellar ataxiaGiulia Coarelli, Frederic Darios, Emilien Petit, et al.NMR in Biomedicine|January 10, 2018
Expanded neurochemical profile in the early stage of Huntington disease using proton magnetic resonance spectroscopyIsaac M Adanyeguh, Marie-Lorraine Monin, Daisy Rinaldi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2018
The genetic nomenclature of recessive cerebellar ataxiasMalco Rossi, Mathieu Anheim, Alexandra Durr, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|August 16, 2019
KIF1C Variants Are Associated with Hypomyelination, Ataxia, Tremor, and Dystonia in Fraternal TwinsEnrica Marchionni, Aurélie Méneret, Boris Keren, et al.Journal of Huntington'S Disease|February 19, 2019
Contemporary Dance Practice Improves Motor Function and Body Representation in Huntington's Disease: A Pilot StudyIris Trinkler, Philippe Chéhère, Julie Salgues, et al.Neuropsychology|September 14, 2018
Executive impairment is associated with unawareness of neuropsychiatric symptoms in premanifest and early Huntington's diseaseSophie C Andrews, David Craufurd, Alexandra Durr, et al.Trials|March 5, 2026
How to improve statistical power in a trial with SCA2 patients using natural history dataMaylis Tran, Pierre-Emmanuel Poulet, Emilien Petit, et al.Journal of Neurology|May 18, 2012
Tremor-spectrum in spinocerebellar ataxia type 3Cecilia Bonnet, Emmanuelle Apartis, Mathieu Anheim, et al.Neuroimage. Clinical|June 21, 2018
Autosomal dominant cerebellar ataxias: Imaging biomarkers with high effect sizesIsaac M Adanyeguh, Vincent Perlbarg, Pierre-Gilles Henry, et al.Journal of Neurology|March 3, 2006
A new phenotype linked to SPG27 and refinement of the critical region on chromosomePascale Ribai, Giovanni Stevanin, Naima Bouslam, et al.Pageof 33