Neurodegeneration : the molecular pathology of dementia and movement disorders [Elektronisk resurs] / edited by Dennis W. Dickson, Roy O. Weller.
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Dickson, Dennis W. (redaktör/utgivare)
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Weller, Roy O. (redaktör/utgivare)
- ISBN 9781444341225
- 2nd ed.
- Publicerad: Hoboken : John Wiley & Sons, 2011
- Engelska 1 online resource (497 p.)
Innehållsförteckning
Ämnesord
Stäng
- Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders; Contents; List of Contributors; Preface; List of Abbreviations; Part 1: Introduction: Basic Mechanisms of Neurodegeneration; 1: Introduction to Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders; 2: Cell Death and Neurodegeneration; 3: Oxidative Stress and Balance in Neurodegenerative Diseases; 4: Protein Aggregation in Neurodegeneration; 5: Protein Degradation in Neurodegeneration: The Ubiquitin Pathway; 6: Genetics of Neurodegeneration; 7: Transgenic Animal Models of Proteinopathies.
- Part 2: Alzheimer's Disease and Aging8: Clinical Aspects of Alzheimer's Disease; 9: Genetics of Alzheimer's Disease; 10: Neuropathology of Alzheimer's Disease and its Variants; 11: Amyloid-ß Production; 12: Elimination of Amyloid ß from the Brain, its Failure in Alzheimer's Disease and Implications for Therapy; Part 3: Tauopathies; 13: Introduction to the Tauopathies; 14: Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17; 15: Progressive Supranuclear Palsy and Corticobasal Degeneration; 16: Pick's Disease; 17: Argyrophilic Grain Disease.
- 18: Parkinsonism-Dementia Complex of Guam19: Postencephalitic Parkinsonism; Part 4: Synucleinopathies; 20: Introduction to a-Synucleinopathies; 21: Parkinson's Disease; 22: Dementia with Lewy Bodies and Parkinson's Disease Dementia; 23: Lewy Bodies in Conditions other than Disorders of a-Synuclein; 24: Multiple System Atrophy; Part 5: Trinucleotide Repeat Disorders; 25: Introduction to Trinucleotide Repeat Diseases; 26: Huntington's Disease; 27: Spinocerebellar Ataxias; 28: Friedreich's Ataxia; 29: Dentatorubral- pallidoluysian Atrophy; 30: Spinal and Bulbar Muscular Atrophy.
- Part 6: Prion Disorders31: Introduction to Prion Disorders; 32: Sporadic Creutzfeldt-Jakob Disease; 33: Genetic Creutzfeldt-Jakob Disease; 34: Fatal Familial and Sporadic Insomnia; 35: A New Prion Disease: Protease -Sensitive Prionopathy; 36: Variant Creutzfeldt-Jakob Disease; 37: Gerstmann-Sträussler-Scheinker Disease; 38: Kuru; 39: Iatrogenic Creutzfeldt-Jakob Disease; Part 7: Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis/Motor Neuron Disease; 40: Introduction; 41: Frontotemporal Lobar Degeneration with TDP-43 Pathology.
- 42: Neuronal Intermediate Filament Inclusion Disease43: Frontotemporal Lobar Degeneration with FUS Immunoreactive Inclusions; 44: Amyotrophic Lateral Sclerosis, Primary Lateral Sclerosis and Spinal Muscular Atrophy; Part 8: Other Neurodegenerative Disorders; 45: Introduction: Genetic Analysis as a Lumper and Splitter in Neurodegenerative Disease; 46: Inherited Amyloidoses and Neurodegeneration: Familial British Dementia and Familial Danish Dementia; 47: Neurodegeneration with Brain Iron Accumulation; 48: Familial Encephalopathy with Neuroserpin Inclusion Bodies.
- 49: Hereditary Ferritinopathies.
Ämnesord
- Movement disorders. (MeSH)
- Neurodegenerative diseases (MeSH)
- Dementia -- pathology (MeSH)
- Nervous system -- degeneration (MeSH)
- Dementia -- Pathogenesis.
- Dementia -- pathology.
- Movement Disorders -- pathology.
- Movement disorders.
- Nervous system -- Degeneration.
- Neurodegenerative diseases.
Genre
- Electronic books. (LCSH)
Klassifikation
- RC365 .N4527 2011 (LCC)
- 616.8 (DDC)
- Vef (kssb/8 (machine generated))
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