Spinocerebellar Ataxia Type 31 Latest Advances

Long-Term Effects of Annual Intensive Rehabilitation in Patients with Hereditary Pure Cerebellar Ataxia: A 7-year Follow-up Study.

Journal: Cerebellum (London, England)

Published: May 09, 2025

Naphthyridine carbamate dimer ligand induces formation of Z-RNA-like fold of disease-related RNA and exhibits a molecular glue characteristics in crystal lattice formation.

Journal: Nucleic acids research

Published: April 17, 2025

[18F]THK5351 uptake in multiple system atrophy compared with other parkinsonian disorders.

Journal: Journal of neurology

Published: March 14, 2025

A Review of Spinocerebellar Ataxias in Taiwan.

Journal: Acta neurologica Taiwanica

Published: August 26, 2024

Changes in Standing Postural Control Ability in a Case of Spinocerebellar Ataxia Type 31 With Physical Therapy Focusing on the Center of Gravity Sway Variables and Lower Leg Muscle Activity.

Journal: Cureus

Published: December 24, 2023

Incidence of different pressure patterns of spinal cerebellar ataxia and analysis of imaging and genetic diagnosis.

Journal: Open life sciences

Published: August 20, 2023

Prevalence of repeat expansions causing autosomal dominant spinocerebellar ataxias in Hokkaido, the northernmost island of Japan.

Journal: Journal of human genetics

Published: July 14, 2023

Temporal Relationship between Impairment of Cerebellar Motor Learning and Deterioration of Ataxia in Patients with Cerebellar Degeneration.

Journal: Cerebellum (London, England)

Published: March 10, 2023

Abnormal saccade profiles in hereditary spinocerebellar degeneration reveal cerebellar contribution to visually guided saccades.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: January 31, 2023

Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping task.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: January 11, 2023

Synthesis and cloning of long repeat sequences using single-stranded circular DNA.

Journal: Frontiers in bioengineering and biotechnology

Published: December 03, 2022

A small molecule binding to TGGAA pentanucleotide repeats that cause spinocerebellar ataxia type 31.

Journal: Bioorganic & medicinal chemistry letters

Published: October 02, 2022

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Long-Term Effects of Annual Intensive Rehabilitation in Patients with Hereditary Pure Cerebellar Ataxia: A 7-year Follow-up Study.

Long-Term Effects of Annual Intensive Rehabilitation in Patients with Hereditary Pure Cerebellar Ataxia: A 7-year Follow-up Study.

Naphthyridine carbamate dimer ligand induces formation of Z-RNA-like fold of disease-related RNA and exhibits a molecular glue characteristics in crystal lattice formation.

Naphthyridine carbamate dimer ligand induces formation of Z-RNA-like fold of disease-related RNA and exhibits a molecular glue characteristics in crystal lattice formation.

[18F]THK5351 uptake in multiple system atrophy compared with other parkinsonian disorders.

[18F]THK5351 uptake in multiple system atrophy compared with other parkinsonian disorders.

A Review of Spinocerebellar Ataxias in Taiwan.

A Review of Spinocerebellar Ataxias in Taiwan.

Changes in Standing Postural Control Ability in a Case of Spinocerebellar Ataxia Type 31 With Physical Therapy Focusing on the Center of Gravity Sway Variables and Lower Leg Muscle Activity.

Changes in Standing Postural Control Ability in a Case of Spinocerebellar Ataxia Type 31 With Physical Therapy Focusing on the Center of Gravity Sway Variables and Lower Leg Muscle Activity.

Incidence of different pressure patterns of spinal cerebellar ataxia and analysis of imaging and genetic diagnosis.

Incidence of different pressure patterns of spinal cerebellar ataxia and analysis of imaging and genetic diagnosis.

Prevalence of repeat expansions causing autosomal dominant spinocerebellar ataxias in Hokkaido, the northernmost island of Japan.

Prevalence of repeat expansions causing autosomal dominant spinocerebellar ataxias in Hokkaido, the northernmost island of Japan.

Temporal Relationship between Impairment of Cerebellar Motor Learning and Deterioration of Ataxia in Patients with Cerebellar Degeneration.

Temporal Relationship between Impairment of Cerebellar Motor Learning and Deterioration of Ataxia in Patients with Cerebellar Degeneration.

Abnormal saccade profiles in hereditary spinocerebellar degeneration reveal cerebellar contribution to visually guided saccades.

Abnormal saccade profiles in hereditary spinocerebellar degeneration reveal cerebellar contribution to visually guided saccades.

Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping task.

Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping task.

Synthesis and cloning of long repeat sequences using single-stranded circular DNA.

Synthesis and cloning of long repeat sequences using single-stranded circular DNA.

A small molecule binding to TGGAA pentanucleotide repeats that cause spinocerebellar ataxia type 31.

A small molecule binding to TGGAA pentanucleotide repeats that cause spinocerebellar ataxia type 31.