Caterina Mariotti

Scale for the assessment and rating of ataxia

T. Schmitz-Hübsch, Sophie Tézenas du Montcel, L. Baliko et al. · Neurology · 2006 · 1.9K citations

Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28

Daniela Di Bella, Federico Lazzaro, Alfredo Brusco et al. · Nature Genetics · 2010 · 338 citations

Mitochondrial Function, Genetic Disorder, Genetics +4

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

Heike Jacobi, Sophie Tézenas du Montcel, Peter Bauer et al. · The Lancet Neurology · 2015 · 286 citations

Longitudinal Cohort Study, Neurological Disorder, Long-term Disease Progression +4

Dysfunction of the Cholesterol Biosynthetic Pathway in Huntington's Disease

Marta Valenza, Dorotea Rigamonti, Donato Goffredo et al. · Journal of Neuroscience · 2005 · 281 citations · Full text

Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (<scp>MOXIe</scp> Study)

David R. Lynch, Melanie Chin, Martin B. Delatycki et al. · Annals of Neurology · 2020 · 273 citations · Full text