Disease: Spinocerebellar ataxia 25
- A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in Childhood
- Age-related differences of cerebellar cortex and nuclei: MRI findings in healthy controls and its application to spinocerebellar ataxia (SCA6) patients
- Charge transport properties of ideal and natural DNA segments, as mutation detectors
- Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
- Clinical, neuroimaging and genetic findings in children with hereditary ataxia: single center study
- Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient
- Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in Canada
- Effect of speech therapy on quality of life in patients with spinocerebelar ataxia type 3
- Hepatic fibrosis: a manifestation of the liver disease evolution in patients with Ataxia-telangiectasia
- Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
- High-Resolution Motion-corrected 7.0-T MRI to Derive Morphologic Measures from the Human Cerebellum in Vivo
- Liver Assessment in Patients with Ataxia-Telangiectasia: Transient Elastography Detects Early Stages of Steatosis and Fibrosis
- Spinocerebellar ataxia 13 and 25
- Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain
- Spinocerebellar ataxia type 31: A clinical and radiological literature review
- Spinocerebellar ataxia with sensory neuropathy (SCA25)
- Synthesis and cloning of long repeat sequences using single-stranded circular DNA
- Targeted long-read sequencing captures CRISPR editing and AAV integration outcomes in brain
- Therapeutic effects of engineered exosome-based miR-25 and miR-181a treatment in spinocerebellar ataxia type 3 mice by silencing ATXN3