Oligodendrocyte dysfunction contributes to motor deficits and Purkinje cell axonopathy in spinocerebellar ataxia type 1. [PDF]
Lee C +9 more
europepmc +1 more source
Nuclear Lamina Dysfunction and DNA Damage as Drivers of Premature Senescence in a Human Müller Glial Cell Model of Spinocerebellar Ataxia Type 7. [PDF]
Ruiz-Esparza-Palacios V +9 more
europepmc +1 more source
An intronic variant in Ferredoxin Reductase (FDXR) creates a cryptic exon in Quarter Horses with Equine Juvenile Spinocerebellar Ataxia. [PDF]
Brown BN +13 more
europepmc +1 more source
Incorporating Patient Perspectives into a Composite Score for Measuring Disease Progression in Spinocerebellar Ataxia (SCA). [PDF]
Potashman MH +14 more
europepmc +1 more source
Sex-specific disruptions in PKCγ signaling in a mouse model of spinocerebellar ataxia type 14. [PDF]
Wolfe SA +14 more
europepmc +1 more source
Targeting Cognitive Dysfunction in Spinocerebellar Ataxia Type 2 Through Digital Cognitive Training. [PDF]
Vieira AA +7 more
europepmc +1 more source
The Status and Future Directions of Treatments for Polyglutamine Spinocerebellar Ataxia: A Bibliometric and Visual Analysis. [PDF]
Ding S +9 more
europepmc +1 more source
Embryonic spinocerebellar ataxia type 37-associated AUUUC repeat RNA causes neurodevelopmental defects. [PDF]
Castro AF +7 more
europepmc +1 more source
FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B? [PDF]
Laß J +17 more
europepmc +1 more source

