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- 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
- Spinocerebellar Ataxia Precision Panel Overview Indications
- Blueprint Genetics Ataxia Panel
- SBMA, Kennedy Disease) Around the World
- Neurology – Differential Diagnosis
- Diagnosis and Management of Ataxia-Telangiectasia in Resource
- Spinocerebellar Ataxia: Patient and Health Professional Perspectives On
- Reviews Spinocerebellar Ataxia 27: a Review and Characterization of an Evolving Phenotype
- Hereditary Ataxia Multigene Panel Testing
- Diseases of the Nervous System G11.0 – G24.02
- (SCA–12): a Tremor Dominant Disease, Typically Seen in India KK Sinha Neurologist, Ranchi, India
- Clinical and Molecular Advances in Autosomal Dominant Cerebellar Ataxias: from Genotype to Phenotype and Physiopathology
- Amyotrophic Lateral Sclerosis and Spinocerebellar Ataxia Type 2 in a Family with Full CAG Repeat Expansions of ATXN2
- A Brief Review on Spinocerebellar Ataxia and Its Treatment Journal of Neurology Research Reviews & Reports
- SMN Deficiency in Severe Models of Spinal Muscular Atrophy Causes
- Hereditary Spastic Paraplegia: from Diagnosis to Emerging Therapeutic Approaches
- Spinocerebellar Ataxia Type 5 (SCA5)
- Spinocerebellar Ataxia Genetic Testing
- Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease
- Migraine, Ataxia and Epilepsy: a Challenging Spectrum of Genetically Determined Calcium Channelopathies
- MRI Findings in Spinocerebellar Ataxias
- Identification of Novel Compound Heterozygous
- Ataxic Disorders
- Spinocerebellar Ataxias
- Machado-Joseph Disease: from First Descriptions to New Perspectives Conceição Bettencourt1,2,3* and Manuela Lima1,2
- (SCA3)/ Machado-Joseph Disease (MJD) What Is Spinocerebellar Ataxia Type 3?
- SCA2 Presenting As an Ataxia-Parkinsonism-Motor Neuron Disease Syndrome
- Machado-Joseph Disease Presenting As Severe Asymmetric Proximal Neuropathy
- Episodic Ataxia
- A Refractory Head Tremor Appearing After Volatile Anesthesia Combined