Results 171 to 180 of about 71,064 (224)

Oligodendrocyte dysfunction contributes to motor deficits and Purkinje cell axonopathy in spinocerebellar ataxia type 1. [PDF]

open access: yesJ Clin Invest
Lee C   +9 more
europepmc   +1 more source

Spinocerebellar ataxia

open access: yesNeurobiology of Disease, 2018
van der Stijl, Rogier   +2 more
openaire   +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]

open access: yesInt J Mol Sci
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]

open access: yesPLoS Genet
Brown BN   +13 more
europepmc   +1 more source

Incorporating Patient Perspectives into a Composite Score for Measuring Disease Progression in Spinocerebellar Ataxia (SCA). [PDF]

open access: yesNeurol Ther
Potashman MH   +14 more
europepmc   +1 more source

Sex-specific disruptions in PKCγ signaling in a mouse model of spinocerebellar ataxia type 14. [PDF]

open access: yesJCI Insight
Wolfe SA   +14 more
europepmc   +1 more source

Targeting Cognitive Dysfunction in Spinocerebellar Ataxia Type 2 Through Digital Cognitive Training. [PDF]

open access: yesCerebellum
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]

open access: yesCurr Neuropharmacol
Ding S   +9 more
europepmc   +1 more source

Embryonic spinocerebellar ataxia type 37-associated AUUUC repeat RNA causes neurodevelopmental defects. [PDF]

open access: yesDis Model Mech
Castro AF   +7 more
europepmc   +1 more source

FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B? [PDF]

open access: yesBrain
Laß J   +17 more
europepmc   +1 more source

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