Spinocerebellar ataxia
Top View
- Phenotypes of Spinocerebellar Ataxia Type 6 and Familial Hemiplegic Migraine Caused by a Unique CACNA1A Missense Mutation in Patients from a Large Family
- Sleep Disorders in Hereditary Ataxias
- Recent Advances in the Treatment of Cerebellar Disorders
- Identifying Therapeutic Targets for Spinocerebellar Ataxia Type 3/Machado–Joseph Disease Through Integration of Pathological Biomarkers and Therapeutic Strategies
- Two Distinct Phenotypes, Hemiplegic Migraine and Episodic Ataxia Type 2, Caused by a Novel Common CACNA1A Variant
- Molecular Mechanism(S) Underlying Neurodegeneration in SCA7 Disease
- Vestibulo-Ocular Arreflexia in Families with Spinocerebellar Ataxia Type 3 (Machado-Joseph Disease) C R Gordon, V Joffe, G Vainstein, N Gadoth
- Mechanisms of the CAG Repeat Mutation in Spinocerebellar Ataxia Type 1 Cara Kraus-Perrotta1 and Sarita Lagalwar2*
- Muscle Excitability Abnormalities in Machado-Joseph Disease
- A Longitudinal DTI Study
- Trends in the Epidemiology of Spinocerebellar Ataxia Type 3/ Machado-Joseph Disease in the Azores Islands, Portugal
- Dementia and Delirium in 4 Patients with Machado-Joseph Disease
- Autosomal Dominant Spinocerebellar Ataxias
- Redalyc.Cognitive Dysfunction in Spinocerebellar Ataxias
- Hereditary Ataxias: Overview
- Spinocerebellar Ataxia Type 2 with Glial Cell Cytoplasmic Inclusions S Probst-Cousin, T Acker, J T Epplen, M Bergmann, K H Plate, B Neundo¨Rfer, D Heuss
- Spinocerebellar Ataxia: Making an Informed Choice About Genetic Testing
- Next-Generation Sequencing Approach to Hyperckemia: a 2-Year Cohort Study E352