Harding Ataxia Latest Advances
Find the Latest Research About Harding Ataxia
Last Updated: 02/24/2026
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Found 52 publications
Overexpression of bank vole PrP(I109) in mice induces a spontaneous atypical prion disease with sex-dependent onset, early NfL elevation, and universal prion strain permissiveness.
Journal: Acta neuropathologica communications
Published: August 26, 2025
No evidence for association between GAA-FGF14 expansion and early onset cerebellar ataxia: a study on 85 undiagnosed patients.
Journal: Journal of neurology
Published: October 09, 2024
Early onset ataxia with comorbid myoclonus and epilepsy: A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 20, 2022
Responsiveness of the Scale for the Assessment and Rating of Ataxia and Natural History in 884 Recessive and Early Onset Ataxia Patients.
Journal: Annals of neurology
Published: October 04, 2022
ATP1A3-related early childhood onset developmental and epileptic encephalopathy responding to corpus callosotomy: A case report.
Journal: Brain & development
Published: February 20, 2022
Editorial commentary on "Instrumented classification of patients with early onset ataxia or developmental coordination disorder and healthy control children".
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: September 23, 2021
Nystagmus may be the first neurological sign in early stages of spinocerebellar ataxia type 3.
Journal: Arquivos de neuro-psiquiatria
Published: November 04, 2020
Instrumented classification of patients with early onset ataxia or developmental coordination disorder and healthy control children combining information from three upper limb SARA tests.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: November 03, 2020
Anti-glutamic acid decarboxylase antibody (GAD) syndromes may have more aggressive disease course in African Americans and early onset of presentation compare to Caucasians group.
Journal: eNeurologicalSci
Published: August 29, 2019
Last Updated: 02/24/2026