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Movement Disorders : Official Journal of the Movement Disorder Society|January 20, 2021
Composite UHDRS Correlates With Progression of Imaging Biomarkers in Huntington's DiseaseCarlos Estevez-Fraga, Rachael I Scahill, Alexandra Durr, et al.Parkinsonism & Related Disorders|March 9, 2019
Combined cerebral atrophy score in Huntington's disease based on atlas-based MRI volumetry: Sample size calculations for clinical trialsHans-Peter Müller, Hans-Jürgen Huppertz, Jens Dreyhaupt, et al.Journal of Neurology|February 19, 2009
SPG11 spastic paraplegia. A new cause of juvenile parkinsonismMathieu Anheim, Clotilde Lagier-Tourenne, Giovanni Stevanin, et al.Archives of Neurology|August 18, 2004
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, et al.Human Brain Mapping|April 24, 2018
Natural biological variation of white matter microstructure is accentuated in Huntington's diseaseSarah Gregory, Helen Crawford, Kiran Seunarine, et al.Plos One|February 14, 2013
Mapping cortico-striatal connectivity onto the cortical surface: a new tractography-based approach to study Huntington diseaseLinda Marrakchi-Kacem, Christine Delmaire, Pamela Guevara, et al.EMBO Molecular Medicine|January 10, 2013
The Huntington disease protein accelerates breast tumour development and metastasis through ErbB2/HER2 signallingCristovão Moreira Sousa, John Russel McGuire, Morgane Sonia Thion, et al.Plos One|February 13, 2016
A Computational Cognitive Biomarker for Early-Stage Huntington's DiseaseThomas V Wiecki, Chrystalina A Antoniades, Alexander Stevenson, et al.Neurology|March 10, 2022
Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 1Carlo Wilke, David Mengel, Ludger Schöls, et al.Cerebellum (London, England)|November 1, 2017
Personality and Neuropsychological Profiles in Friedreich AtaxiaSabrina Sayah, Jean-Yves Rotgé, Hélène Francisque, et al.Pageof 33