Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics

Neurodegenerative diseases are major contributors to disability and disease, with Alzheimer's and Parkinson's diseases the most prevalent. This major reference reviews the rapidly advancing knowledge of pathogenesis and treatment of neurodegenerative diseases in the context of a comprehens...

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Weitere Verfasser: Beal, M. Flint 1950- (HerausgeberIn), Lang, Anthony E. (HerausgeberIn), Ludolph, Albert C. 1953- (HerausgeberIn)
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Veröffentlicht: Cambridge Cambridge University Press 2005
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505 8 |a Friedreich's ataxia and other autosomal recessive ataxias -- Ataxia telangiectasia -- An approach to the patient with motor neuron dysfunction -- The genetics of amyotrophic lateral sclerosis -- Current and potential therapeutics in motor neuron diseases -- The hereditary spastic paraplegias -- Spinal and bulbar muscular atrophy (Kennedy's disease): a sex-limited, polyglutamine repeat expansion disorder -- Spinal muscular atrophies -- Western Pacific ALS/parkinsonism-dementia complex -- Huntington's disease -- Dentatorubral-pallidoluysian atrophy (DRPLA): model for Huntington's disease and other polyglutamine diseases -- Neurocanthocytosis -- Brain iron disorders -- Neurological aspects of Wilson's disease -- Disorders of the mitochondrial respiratory chain 
505 8 |a The neuropathology of Alzheimer's disease in the year 2005 -- Genetics of Alzheimer's disease -- The role of [beta]-amyloid in Alzheimer's disease -- Treatment of Alzheimer's disease -- Dementia with Lewy bodies -- Frontotemporal lobar degeneration -- Frontotemporal dementia with parkinsonism linked to chromosome 17 -- Prion diseases -- Approach to the patient presenting with parkinsonism -- Parkinson's disease -- Neuropathology of Parkinson's disease -- Genetics of parkinsonism -- Pathophysiology: biochemistry of Parkinson's disease -- Current and potential treatments of Parkinson's disease -- Current and potential treatments of Parkonson's disease -- Multiple system atrophy -- Progressive supranuclear palsy -- Corticobasal degeneration -- Approach to the patient with ataxia -- Autosomal dominant cerebellar ataxia 
505 8 |a Toxic animal models -- A genetic outline of the pathways to cell death in Alzheimer's disease, Parkinson's disease, frontal dementias and related disorders -- Neurophysiology of Parkinson's disease, levodopa-induced dyskinesias, dystonia, Huntington's disease and muyoclonus -- Structural and functional magnetic resonance imaging in neurodegenerative diseases -- PET/SPECT -- Magnetic resonance spectroscopy of neurodegenerative illness -- Gene therapy -- Stem cells and cell-based theapy in neurodegenerative disease -- Necessary methodological and stem cell advances for restoration of the dopaminergic system in Parkinson's disease patients -- Clinical aspects of normal aging -- Neuropathology of normal aging in cerebral cortex -- Mild cognitive impairment -- Alzheimer's disease: overview 
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Datensatz im Suchindex

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Lang, Anthony E.
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contents Endogenous free radicals and antioxidants in the brain -- Biological oxidants and therapeutic antioxidants -- Mitochondria, metabolic inhibitors and neurodegeneration -- Excitoxicity and excitatory amino acid antagonists in chronic neurodegenerative diseases -- Glutamate transporters -- Calcium binding proteins in selective vulnerability of motor neurons -- Apoptosis in neurodegenerative diseases -- Neurotrophic factors -- Protein misfolding and cellular defense mechanisms in neurodegenerative diseases -- Neurodegenerative disease and the repair of oxidatively damaged DNA -- Compounds acting on ion channels -- The role of nitric oxide and PARP in neuronal cell death -- Copper and zinc in Alzheimer's disease and amyotrophic lateral sclerosis -- The role of inflammation in Alzheimer's disease neuropathology and clinical dementia. From epidemiology to treatment -- Selected genetically engineered models relevant to human neurodegenerative disease
Friedreich's ataxia and other autosomal recessive ataxias -- Ataxia telangiectasia -- An approach to the patient with motor neuron dysfunction -- The genetics of amyotrophic lateral sclerosis -- Current and potential therapeutics in motor neuron diseases -- The hereditary spastic paraplegias -- Spinal and bulbar muscular atrophy (Kennedy's disease): a sex-limited, polyglutamine repeat expansion disorder -- Spinal muscular atrophies -- Western Pacific ALS/parkinsonism-dementia complex -- Huntington's disease -- Dentatorubral-pallidoluysian atrophy (DRPLA): model for Huntington's disease and other polyglutamine diseases -- Neurocanthocytosis -- Brain iron disorders -- Neurological aspects of Wilson's disease -- Disorders of the mitochondrial respiratory chain
The neuropathology of Alzheimer's disease in the year 2005 -- Genetics of Alzheimer's disease -- The role of [beta]-amyloid in Alzheimer's disease -- Treatment of Alzheimer's disease -- Dementia with Lewy bodies -- Frontotemporal lobar degeneration -- Frontotemporal dementia with parkinsonism linked to chromosome 17 -- Prion diseases -- Approach to the patient presenting with parkinsonism -- Parkinson's disease -- Neuropathology of Parkinson's disease -- Genetics of parkinsonism -- Pathophysiology: biochemistry of Parkinson's disease -- Current and potential treatments of Parkinson's disease -- Current and potential treatments of Parkonson's disease -- Multiple system atrophy -- Progressive supranuclear palsy -- Corticobasal degeneration -- Approach to the patient with ataxia -- Autosomal dominant cerebellar ataxia
Toxic animal models -- A genetic outline of the pathways to cell death in Alzheimer's disease, Parkinson's disease, frontal dementias and related disorders -- Neurophysiology of Parkinson's disease, levodopa-induced dyskinesias, dystonia, Huntington's disease and muyoclonus -- Structural and functional magnetic resonance imaging in neurodegenerative diseases -- PET/SPECT -- Magnetic resonance spectroscopy of neurodegenerative illness -- Gene therapy -- Stem cells and cell-based theapy in neurodegenerative disease -- Necessary methodological and stem cell advances for restoration of the dopaminergic system in Parkinson's disease patients -- Clinical aspects of normal aging -- Neuropathology of normal aging in cerebral cortex -- Mild cognitive impairment -- Alzheimer's disease: overview
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Cambridge Cambridge University Press 2005
1 online resource (xxii, 985 pages)
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Title from publisher's bibliographic system (viewed on 05 Oct 2015)
Endogenous free radicals and antioxidants in the brain -- Biological oxidants and therapeutic antioxidants -- Mitochondria, metabolic inhibitors and neurodegeneration -- Excitoxicity and excitatory amino acid antagonists in chronic neurodegenerative diseases -- Glutamate transporters -- Calcium binding proteins in selective vulnerability of motor neurons -- Apoptosis in neurodegenerative diseases -- Neurotrophic factors -- Protein misfolding and cellular defense mechanisms in neurodegenerative diseases -- Neurodegenerative disease and the repair of oxidatively damaged DNA -- Compounds acting on ion channels -- The role of nitric oxide and PARP in neuronal cell death -- Copper and zinc in Alzheimer's disease and amyotrophic lateral sclerosis -- The role of inflammation in Alzheimer's disease neuropathology and clinical dementia. From epidemiology to treatment -- Selected genetically engineered models relevant to human neurodegenerative disease
Friedreich's ataxia and other autosomal recessive ataxias -- Ataxia telangiectasia -- An approach to the patient with motor neuron dysfunction -- The genetics of amyotrophic lateral sclerosis -- Current and potential therapeutics in motor neuron diseases -- The hereditary spastic paraplegias -- Spinal and bulbar muscular atrophy (Kennedy's disease): a sex-limited, polyglutamine repeat expansion disorder -- Spinal muscular atrophies -- Western Pacific ALS/parkinsonism-dementia complex -- Huntington's disease -- Dentatorubral-pallidoluysian atrophy (DRPLA): model for Huntington's disease and other polyglutamine diseases -- Neurocanthocytosis -- Brain iron disorders -- Neurological aspects of Wilson's disease -- Disorders of the mitochondrial respiratory chain
The neuropathology of Alzheimer's disease in the year 2005 -- Genetics of Alzheimer's disease -- The role of [beta]-amyloid in Alzheimer's disease -- Treatment of Alzheimer's disease -- Dementia with Lewy bodies -- Frontotemporal lobar degeneration -- Frontotemporal dementia with parkinsonism linked to chromosome 17 -- Prion diseases -- Approach to the patient presenting with parkinsonism -- Parkinson's disease -- Neuropathology of Parkinson's disease -- Genetics of parkinsonism -- Pathophysiology: biochemistry of Parkinson's disease -- Current and potential treatments of Parkinson's disease -- Current and potential treatments of Parkonson's disease -- Multiple system atrophy -- Progressive supranuclear palsy -- Corticobasal degeneration -- Approach to the patient with ataxia -- Autosomal dominant cerebellar ataxia
Toxic animal models -- A genetic outline of the pathways to cell death in Alzheimer's disease, Parkinson's disease, frontal dementias and related disorders -- Neurophysiology of Parkinson's disease, levodopa-induced dyskinesias, dystonia, Huntington's disease and muyoclonus -- Structural and functional magnetic resonance imaging in neurodegenerative diseases -- PET/SPECT -- Magnetic resonance spectroscopy of neurodegenerative illness -- Gene therapy -- Stem cells and cell-based theapy in neurodegenerative disease -- Necessary methodological and stem cell advances for restoration of the dopaminergic system in Parkinson's disease patients -- Clinical aspects of normal aging -- Neuropathology of normal aging in cerebral cortex -- Mild cognitive impairment -- Alzheimer's disease: overview
Neurodegenerative diseases are major contributors to disability and disease, with Alzheimer's and Parkinson's diseases the most prevalent. This major reference reviews the rapidly advancing knowledge of pathogenesis and treatment of neurodegenerative diseases in the context of a comprehensive survey of each disease and its clinical features. The editors and contributors are among the leading experts in the field internationally. Covering basic science, diagnostic tools and therapeutic approaches, the book focuses on all aspects of neurodegenerative disease, including the normal aging process. The dementias, prion diseases, Parkinson's disease and atypical parkinsonisms, neurodegenerative ataxias, motor neuron diseases, degenerative diseases with chorea, iron and copper disorders, and mitochondrial diseases, are all methodically presented and discussed, with extensive illustrations. In each case the underlying genetics, neuropathological and clinical issues are fully reviewed, making this the most complete as well as the most authoritative reference available to clinicians and neuroscientists
Nervous system / Degeneration
Nervous system / Diseases / Treatment
Nervendegeneration (DE-588)4300182-8 gnd rswk-swf
Nervendegeneration (DE-588)4300182-8 s
1\p DE-604
Beal, M. Flint 1950- (DE-588)124005969 edt
Lang, Anthony E. edt
Ludolph, Albert C. 1953- (DE-588)1081317531 edt
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https://doi.org/10.1017/CBO9780511544873 Verlag URL des Erstveröffentlichers Volltext
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spellingShingle Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics
Endogenous free radicals and antioxidants in the brain -- Biological oxidants and therapeutic antioxidants -- Mitochondria, metabolic inhibitors and neurodegeneration -- Excitoxicity and excitatory amino acid antagonists in chronic neurodegenerative diseases -- Glutamate transporters -- Calcium binding proteins in selective vulnerability of motor neurons -- Apoptosis in neurodegenerative diseases -- Neurotrophic factors -- Protein misfolding and cellular defense mechanisms in neurodegenerative diseases -- Neurodegenerative disease and the repair of oxidatively damaged DNA -- Compounds acting on ion channels -- The role of nitric oxide and PARP in neuronal cell death -- Copper and zinc in Alzheimer's disease and amyotrophic lateral sclerosis -- The role of inflammation in Alzheimer's disease neuropathology and clinical dementia. From epidemiology to treatment -- Selected genetically engineered models relevant to human neurodegenerative disease
Friedreich's ataxia and other autosomal recessive ataxias -- Ataxia telangiectasia -- An approach to the patient with motor neuron dysfunction -- The genetics of amyotrophic lateral sclerosis -- Current and potential therapeutics in motor neuron diseases -- The hereditary spastic paraplegias -- Spinal and bulbar muscular atrophy (Kennedy's disease): a sex-limited, polyglutamine repeat expansion disorder -- Spinal muscular atrophies -- Western Pacific ALS/parkinsonism-dementia complex -- Huntington's disease -- Dentatorubral-pallidoluysian atrophy (DRPLA): model for Huntington's disease and other polyglutamine diseases -- Neurocanthocytosis -- Brain iron disorders -- Neurological aspects of Wilson's disease -- Disorders of the mitochondrial respiratory chain
The neuropathology of Alzheimer's disease in the year 2005 -- Genetics of Alzheimer's disease -- The role of [beta]-amyloid in Alzheimer's disease -- Treatment of Alzheimer's disease -- Dementia with Lewy bodies -- Frontotemporal lobar degeneration -- Frontotemporal dementia with parkinsonism linked to chromosome 17 -- Prion diseases -- Approach to the patient presenting with parkinsonism -- Parkinson's disease -- Neuropathology of Parkinson's disease -- Genetics of parkinsonism -- Pathophysiology: biochemistry of Parkinson's disease -- Current and potential treatments of Parkinson's disease -- Current and potential treatments of Parkonson's disease -- Multiple system atrophy -- Progressive supranuclear palsy -- Corticobasal degeneration -- Approach to the patient with ataxia -- Autosomal dominant cerebellar ataxia
Toxic animal models -- A genetic outline of the pathways to cell death in Alzheimer's disease, Parkinson's disease, frontal dementias and related disorders -- Neurophysiology of Parkinson's disease, levodopa-induced dyskinesias, dystonia, Huntington's disease and muyoclonus -- Structural and functional magnetic resonance imaging in neurodegenerative diseases -- PET/SPECT -- Magnetic resonance spectroscopy of neurodegenerative illness -- Gene therapy -- Stem cells and cell-based theapy in neurodegenerative disease -- Necessary methodological and stem cell advances for restoration of the dopaminergic system in Parkinson's disease patients -- Clinical aspects of normal aging -- Neuropathology of normal aging in cerebral cortex -- Mild cognitive impairment -- Alzheimer's disease: overview
Nervous system / Degeneration
Nervous system / Diseases / Treatment
Nervendegeneration (DE-588)4300182-8 gnd
subject_GND (DE-588)4300182-8
title Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics
title_auth Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics
title_exact_search Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics
title_full Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics [edited by] M. Flint Beal, Anthony E. Lang, Albert C. Ludolph
title_fullStr Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics [edited by] M. Flint Beal, Anthony E. Lang, Albert C. Ludolph
title_full_unstemmed Neurodegenerative diseases neurobiology, pathogenesis, and therapeutics [edited by] M. Flint Beal, Anthony E. Lang, Albert C. Ludolph
title_short Neurodegenerative diseases
title_sort neurodegenerative diseases neurobiology pathogenesis and therapeutics
title_sub neurobiology, pathogenesis, and therapeutics
topic Nervous system / Degeneration
Nervous system / Diseases / Treatment
Nervendegeneration (DE-588)4300182-8 gnd
topic_facet Nervous system / Degeneration
Nervous system / Diseases / Treatment
Nervendegeneration
url https://doi.org/10.1017/CBO9780511544873
work_keys_str_mv AT bealmflint neurodegenerativediseasesneurobiologypathogenesisandtherapeutics
AT langanthonye neurodegenerativediseasesneurobiologypathogenesisandtherapeutics
AT ludolphalbertc neurodegenerativediseasesneurobiologypathogenesisandtherapeutics