22 results on '"La Spada, Albert R."'
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2. Contributors
3. Spinocerebellar Ataxia Type 7: From Mechanistic Pathways to Therapeutic Opportunities
4. Chapter 12 - Selective vulnerability in Huntington's disease: From excitotoxicity, mitochondrial dysfunction, and transcription dysregulation to therapeutic opportunity
5. X-Linked Spinal and Bulbar Muscular Atrophy: From Clinical Genetic Features and Molecular Pathology to Mechanisms Underlying Disease Toxicity
6. List of Contributors
7. Senataxin, A Novel Helicase at the Interface of RNA Transcriptome Regulation and Neurobiology: From Normal Function to Pathological Roles in Motor Neuron Disease and Cerebellar Degeneration
8. Huntington’s Disease and Other Polyglutamine Repeat Diseases
9. The CAG–polyglutamine repeat diseases: a clinical, molecular, genetic, and pathophysiologic nosology
10. Motor Neuron Differentiation from Pluripotent Stem Cells: Development of the Technique, Synopsis of Protocols, and Summary of Current Applications
11. Transcription Modulation of Mitochondrial Function and Related Pathways as a Therapeutic Opportunity in Parkinson’s Disease
12. List of Contributors
13. Cellular and Molecular Basis of Neurodegeneration in the CAG–Polyglutamine Repeat Diseases
14. Contributors
15. Spinocerebellar Ataxia Type 7: Clinical Features to Cellular Pathogenesis
16. Spinal and bulbar muscular atrophy (Kennedy's disease): a sex-limited, polyglutamine repeat expansion disorder
17. Trinucleotide Repeat Disorders
18. Kennedy's Disease
19. Chapter 11 - The CAG–polyglutamine repeat diseases: a clinical, molecular, genetic, and pathophysiologic nosology
20. Chapter 7 - Huntington’s Disease and Other Polyglutamine Repeat Diseases: Molecular Mechanisms and Pathogenic Pathways
21. Chapter 27 - Spinocerebellar Ataxia Type 7: Clinical Features to Cellular Pathogenesis
22. Chapter 48 - Cellular and Molecular Basis of Neurodegeneration in the CAG–Polyglutamine Repeat Diseases
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