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Cerebellum (London, England)|June 23, 2026
Transitional Life Events in Friedreich Ataxia: Differential Age at Onset PerspectivesAudrey Iskandar, Maresa Buchholz, Dorota Sarwinska, et al.Nature Communications|September 3, 2024
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansionsLars Mohren, Friedrich Erdlenbruch, Elsa Leitão, et al.Nature Genetics|April 29, 2024
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagyKarla P Figueroa, Caspar Gross, Elena Buena-Atienza, et al.Acta Neuropathologica Communications|July 19, 2025
Influence of ATXN2 intermediate CAG repeats, 9bp duplication and alternative splicing on SCA3 pathogenesisMarilena Lauerer, Jennifer Faber, Nicolas Casadei, et al.Journal of Neurology|December 12, 2024
Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3Tim Lukas Elter, Daniel Sturm, Magda M Santana, et al.Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Progression of biological markers in spinocerebellar ataxia type 3: analysis of longitudinal data from the ESMI cohortMoritz Berger, Hector Garcia-Moreno, Monica Ferreira, et al.The Lancet Regional Health. Europe|July 18, 2025
Progression of biological markers in spinocerebellar ataxia type 3: longitudinal analysis of prospective data from the ESMI cohortMoritz Berger, Hector Garcia-Moreno, Mónica Ferreira, et al.Pageof 2