Spinocerebellar ataxia

14 papers, ranked 1 hour ago

Efficacy and Safety of DL-3-n-Butylphthalide in Spinocerebellar Ataxia Type 3

Shen et al. · Movement disorders : official journal of the Movement Disorder Society · 15 Sep 2026

6 days old
key journal in field

score 74

Selectivity Filter KCND3 Variant Causes Spinocerebellar Ataxia 19/22 and K(V)4.3 Functional Loss

Lee et al. · Movement disorders : official journal of the Movement Disorder Society · 9 Sep 2026

2 weeks old
key journal in field

score 72

Transcranial alternating current stimulation for treatment of multiple system atrophy cerebellar type: A randomized controlled trial

Chen et al. · Brain stimulation · 9 Sep 2026

2 weeks old
key journal in field

score 72

Myeloid cell replacement induces intercellular mitochondrial transfer and restores metabolism in a mouse model of mitochondrial disease

Cho et al. · Nature communications · 15 Aug 2026

5 weeks old
flagship journal in field

score 71

Characterising the motif composition and allele length distribution of ZFHX3 GGC repeat expansions in amyotrophic lateral sclerosis

Zussa et al. · Journal of human genetics · 15 Sep 2026

6 days old

score 67

Convergent validity, responsiveness, and meaningful within-subject change of the PROM-Ataxia in spinocerebellar ataxias

Leeuwenberg et al. · Journal of neurology · 9 Sep 2026

2 weeks old

score 65

Digital Balance Biomarkers and Interpretable Evaluation of Disease Severity in Spinocerebellar Ataxia Type 3

Zhang et al. · Annals of the New York Academy of Sciences · 1 Sep 2026

3 weeks old

score 63

PolyQ-expanded ataxin-3 is associated with mitochondrial alterations in Machado-Joseph disease

Simó et al. · Disease models & mechanisms · 1 Sep 2026

3 weeks old

score 63

Orbital lymphoma presenting as preseptal cellulitis in a child with ataxia-telangiectasia

AlNasser et al. · BMJ case reports · 17 Sep 2026

4 days old
case report

score 38

Expanding the phenotypic spectrum of spinocerebellar ataxia type 7: angioid streaks and intrafamilial phenotypic variability

Cao et al. · Journal of neurology · 11 Sep 2026

1 weeks old
letter

score 36

Ataxia with oculomotor apraxia type 2 due to the new compound heterozygous variants c.5825T>C (inherited) and c.6106+1G>T (de novo) in SETX

Fiorini et al. · Clinics (Sao Paulo, Brazil) · 8 Sep 2026

2 weeks old
letter

score 35

Downbeat nystagmus without ataxia as an early manifestation of spinocerebellar ataxia, autosomal recessive type 10 (SCAR10): a case report

Stearns et al. · Neurogenetics · 6 Sep 2026

2 weeks old
case report

score 34

FGF14 (GAA) repeat expansion-associated Ataxia (SCA27B): Expanding the clinical and diagnostic spectrum from the first genetically confirmed case in Argentina

Gatto et al. · Parkinsonism & related disorders · 1 Sep 2026

3 weeks old
letter

score 33

Continuous subcutaneous foscarbidopa/foslevodopa infusion as a therapeutic option in spinocerebellar ataxia type 8 presenting with early-onset parkinsonism

Onorati et al. · Clinical parkinsonism & related disorders · 1 Jan 2026

9 months old
case report

score 20

The query

("Spinocerebellar Ataxias"[MeSH Terms] OR "Spinocerebellar Degenerations"[MeSH Terms] OR "Machado-Joseph Disease"[MeSH Terms] OR "spinocerebellar ataxia"[Title/Abstract] OR "ataxin"[Title/Abstract])