Somatosensory Evoked Potentials in Spinocerebellar Ataxia Type 3 and Type 10. [PDF]
Coutinho L +11 more
europepmc +1 more source
Developing an antisense oligonucleotide treatment for Spinocerebellar Ataxia Type 3
Spinocerebellar ataxia type 3 (SCA3) is a hereditary neurodegenerative disorder caused by a CAG triplet repeat expansion in the ATXN3 gene. This expanded CAG repeat is translated into a toxic polyglutamine repeat in the ataxin-3 protein.
Toonen, L.J.A.
core
IGFBP1 as a metabolic-neurodegenerative biomarker in spinocerebellar ataxia type 3. [PDF]
Chiu C +8 more
europepmc +1 more source
Relationship of subclinical lung injury to chronic airway inflammation in spinocerebellar ataxia type 3. [PDF]
Lv XT +11 more
europepmc +1 more source
Association of spinocerebellar ataxia type 3 and spinocerebellar ataxia type 8 microsatellite expansions: Genetic counseling implications [PDF]
Sabrina Paganoni +3 more
openaire +1 more source
Rad23b exacerbates pathological aggregates through disrupting proteasome functions in Spinocerebellar ataxia type 3. [PDF]
Chen YC +6 more
europepmc +1 more source
Association Between Cerebellar Metabolic Markers and Activities of Daily Living in Patients With Spinocerebellar Ataxia Type 3. [PDF]
Ye M +6 more
europepmc +1 more source
Peripheral and autonomic nervous system involvement in spinocerebellar ataxia type 3: unveiling an invisible burden. [PDF]
Leeuwenberg KE +3 more
europepmc +1 more source
Extracellular vesicles-mediated delivery of SpCas9 RNPs for therapeutic gene editing in Spinocerebellar Ataxia Type 3. [PDF]
Leandro K +15 more
europepmc +1 more source
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichment. [PDF]
Baumeister H +39 more
europepmc +1 more source

