• <em>SYNE1</em>-related autosomal recessive cerebellar ataxia, congenital cerebellar hypoplasia, and cognitive impairment
• A Case of Two Repeats: Huntington's Disease and Spinocerebellar Ataxia Type 8
• Accelerated replicative senescence of ataxia-telangiectasia skin fibroblasts is retained at physiologic oxygen levels, with unique and common transcriptional patterns
• As Frequent as Polyglutamine Spinocerebellar Ataxias: SCA27B in a Large German Autosomal Dominant Ataxia Cohort
• Autosomal dominant cerebellar ataxias: new genes and progress towards treatments
• Coexistence of multiple sclerosis and spinocerebellar ataxia type-8
• Dexamethasone induces p21^cip1/waf1 expression via FoxO3a independently of the Lamin A/C-HDAC2 interaction in Ataxia Telangiectasia
• Epilepsy in spinocerebellar ataxia type 8: a case report
• Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China
• Genetic Epidemiology and Clinical Characteristics of Patients with Spinocerebellar Ataxias in an Unexplored Brazilian State, Using Strategies for Resource-Limited Settings
• Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report
• Identification of Abnormal 51 CTA/CTG Expansion as Probably the Shortest Pathogenic Allele for Spinocerebellar Ataxia-8 in China
• Implications of specific lysine residues within ataxin-3 for the molecular pathogenesis of Machado-Joseph disease
• Interrater Reliability of the Scale for the Assessment and Rating of Ataxia, Berg Balance Scale, and Functional Independence Measure Motor Domain in Individuals With Hereditary Cerebellar Ataxia
• Mechanisms of repeat-associated non-AUG translation in neurological microsatellite expansion disorders
• Neurocutaneous Syndromes, Perinatal Factors, and the Risk of Childhood Cancer in Sweden
• Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy
• PSP-Phenotype in SCA8: Case Report and Systemic Review
• SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F
• Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects
• Spastic paraplegia is the main manifestation of a spinocerebellar ataxia type 8 lineage in China: a case report and review of literature
• Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain
• Spinocerebellar Ataxia Type 1 Characteristics in Patient-Derived Fibroblast and iPSC-Derived Neuronal Cultures
• Spinocerebellar ataxia type 8 in Russian patients
• Spinocerebellar ataxia type 8 presents as progressive supranuclear palsy
• Spoonbill positively regulates JNK signalling mediated apoptosis in Drosophila melanogaster
• The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins
• The RNA binding KH domain of Spoonbill depletes pathogenic non-coding spinocerebellar ataxia 8 transcripts and suppresses neurodegeneration in Drosophila
• Therapeutic Strategies for Spinocerebellar Ataxia Type 1
• Unstable repeat expansion in major psychiatric disorders: two decades on, is dynamic DNA back on the menu?