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Human Brain Mapping|October 11, 2015
Large-scale brain network abnormalities in Huntington's disease revealed by structural covarianceLora Minkova, Simon B Eickhoff, Ahmed Abdulkadir, et al.Neurology|August 20, 2025
Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar AtaxiasEmilien Petit, Daniel López Domínguez, Cecilia Marelli, et al.Therapie|January 4, 2026
How to differentiate between clinical added value (CAV) V drugs: What are the implications, and what is the access pathway?Clémentine Body, Frédéric Chassagnol, Driss Berdaï, et al.Plos Genetics|January 22, 2010
Altered gene expression and DNA damage in peripheral blood cells from Friedreich's ataxia patients: cellular model of pathologyAstrid C Haugen, Nicholas A Di Prospero, Joel S Parker, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 30, 2010
Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindredsPeter Bauer, Giovanni Stevanin, Christian Beetz, et al.The Lancet. Neurology|June 12, 2017
Neurofilament light protein in blood as a potential biomarker of neurodegeneration in Huntington's disease: a retrospective cohort analysisLauren M Byrne, Filipe B Rodrigues, Kaj Blennow, et al.Human Molecular Genetics|December 24, 2016
Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylationJulie Lavie, Román Serrat, Nadège Bellance, et al.Neurology|January 26, 2018
Neurofilament light protein in blood predicts regional atrophy in Huntington diseaseEileanoir B Johnson, Lauren M Byrne, Sarah Gregory, et al.Annals of Physical and Rehabilitation Medicine|April 7, 2023
Individual perception of environmental factors that influence lower limbs spasticity in inherited spastic paraparesisPauline Lallemant-Dudek, Livia Parodi, Giulia Coarelli, et al.Human Brain Mapping|March 16, 2017
Structural and functional brain network correlates of depressive symptoms in premanifest Huntington's diseasePeter McColgan, Adeel Razi, Sarah Gregory, et al.Pageof 33