| Document Type
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BL
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| Record Number
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664511
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| Doc. No
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dltt
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| Title & Author
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Neurodegeneration : : the molecular pathology of dementia and movement disorders /\ edited by Dennis W. Dickson, Roy O. Weller
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| Edition Statement
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2nd ed
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| Publication Statement
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Chichester, West Sussex ;Hoboken, NJ :: Wiley-Blackwell,, 2011
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| Page. NO
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xvii, 477 p. :: ill. (some col.) ;; 29 cm
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| ISBN
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9781405196932 (hardcover : alk. paper)
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: 1405196939 (hardcover : alk. paper)
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: 9781444341225 (ePDF)
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: 1444341227 (ePDF)
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: 9781444341256 (Wiley Online Library)
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: 1444341251 (Wiley Online Library)
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: 9781444341232 (ePub)
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: 1444341235 (ePub)
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| Bibliographies/Indexes
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Includes bibliographical references and index
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| Contents
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Introduction to neurodegeneration: the molecular pathology of dementia and movement disorders -- Cell death and neurodegeneration -- Oxidative stress and balance in neurodegenerative diseases -- Protein aggregation in neurodegeneration -- Protein degradation in neurodegeneration: the ubiquitin pathway -- Genetics of neurodegeneration -- Transgenic animal models of proteinopathies -- Clinical aspects of Alzheimer's Disease -- Genetics of Alzheimer's Disease -- Neuropathology of Alzheimer's Disease and its variants -- Amyloid-B production -- Elimination of amyloid B from the brain, its failure in Alzheimer's Disease and implications for therapy -- Introduction to tauopathies -- Frontotemporal dementia and Parkinsonism linked to chromosome -- Progressive supranuclear palsy and corticobasal degeneration -- Pick's disease -- Argyrophilic grain disease -- Parkinsonism-dementia complex of Guam -- Postencephalitic Parkinsonism -- Introduction to x-Synucleinopathies -- Parkinson's Disease -- Dementia with Lewy Bodies and Parkinson's Disease dementia -- Lewy Bodies in conditions other than disorders of x-Synuclein -- Multiple system atrophy -- Introduction to trinucleotide repeat diseases -- Huntington's Disease -- Spinocerebellar ataxias -- Friedreich's ataxia -- Dentatorubral-pallidoluysian atrophy -- Spinal and bulbar muscular atrophy --
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Introduction to prion disorders -- Sporadic Creutzfeldt-Jakob Disease -- Genetic Creutzfeldt-Jakob Disease -- Fatal familial and sporadic insomnia -- A new prion disease: protease-sensitive prionopathy -- Variant Creutzfeldt-Jakob Disease -- Gerstmann-Straussler--Scheinkler Disease -- Kuru -- Iatrogenic Creutzfeldt-Jakob Disease -- Frontotemporal lobar degeneration with TDP-43 pathology -- Neuronal intermediate filament inclusion disease -- Frontotemporal lobar degeneration with FUS immunoreactive inclusions -- Amyotrophic lateral sclerosis, primary lateral sclerosis and spinal muscular atrophy -- Introduction: genetic analysis as a lumper and splitter in neurodegenerative disease -- Inherited amyloidoses and neurodegeneration: familial British dementia and familial Danish dementia -- Neurodegeneration with brain iron accumulation -- Familial encephalopathy with neuroserpin inclusion bodies -- Hereditary ferritinopathies
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| Subject
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Nervous system-- Degeneration
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Dementia-- Pathogenesis
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Movement disorders
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Neurodegenerative Diseases
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Dementia-- pathology
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Movement Disorders-- pathology
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| Dewey Classification
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616.8
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| LC Classification
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RC365.N4527 2011
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| NLM classification
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2011 L-825
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WL 359
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| Added Entry
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Dickson, Dennis
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