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2015, Sixth edition., ISBN 1608311767, xii, 576 pages
Top experts from all over the world have been brought together by the editors, to give a world of expertise on this important subject, with a strong emphasis... 
Parkinson Disease | Movement Disorders
Book
Parkinsonism & related disorders, ISSN 1353-8020, 1995
Journal
2011, 1. Aufl., ISBN 9781405191852, 498
Parkinson's Disease has traditionally been seen as a movement disorder, and diagnosed by the development of tremor. However, we are beginning to understand... 
Parkinson's disease - Diagnosis | Parkinson's disease
eBook
Annual Review of Neuroscience, ISSN 0147-006X, 2008, Volume 31, Issue 1, pp. 151 - 173
Many major human neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS), display axonal... 
Amyotrophic lateral sclerosis | Parkinson's disease | Huntington's disease | Alzheimer's disease | Charcot-Marie-tooth disease | Motor neuron disease | motor neuron disease | MARIE-TOOTH-DISEASE | ACTIVATED PROTEIN-KINASE | HEREDITARY SPASTIC PARAPLEGIA | GLYCOGEN-SYNTHASE KINASE-3 | AMYOTROPHIC-LATERAL-SCLEROSIS | MOTOR-NEURON DISEASE | MUTANT SUPEROXIDE-DISMUTASE | amyotrophic lateral sclerosis | HUNTINGTIN-ASSOCIATED PROTEIN-1 | NEUROSCIENCES | Charcot-Marie-Tooth disease | NUCLEOTIDE EXCHANGE FACTOR | CYCLIN-DEPENDENT KINASE-5 | Axonal Transport - genetics | Central Nervous System - metabolism | Humans | Central Nervous System - pathology | Charcot-Marie-Tooth Disease - genetics | Motor Neuron Disease - metabolism | Motor Neuron Disease - genetics | Parkinson Disease - metabolism | Motor Neuron Disease - physiopathology | Charcot-Marie-Tooth Disease - metabolism | Huntington Disease - physiopathology | Alzheimer Disease - physiopathology | Axons - metabolism | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Parkinson Disease - physiopathology | Huntington Disease - metabolism | Animals | Neurodegenerative Diseases - physiopathology | Axons - pathology | Alzheimer Disease - metabolism | Huntington Disease - genetics | Central Nervous System - physiopathology | Charcot-Marie-Tooth Disease - physiopathology | Alzheimer Disease - genetics | Nervous system | Degeneration | Axonal transport | Analysis
Journal Article
Science, ISSN 0036-8075, 6/2002, Volume 296, Issue 5575, pp. 1991 - 1995
A broad range of neurodegenerative disorders is characterized by neuronal damage that may be caused by toxic, aggregation-prone proteins. As genes are... 
Nervous system diseases | Reviews | Neurodegenerative diseases | Disease models | Huntington disease | Parkinson disease | Prion diseases | Amyotrophic lateral sclerosis | Nervous system heredodegenerative disorders | Alzheimers disease | Genetic mutation | Parkinson Disease - therapy | Neurons - pathology | Prion Diseases - genetics | Humans | Peptides - genetics | Tauopathies - pathology | Alzheimer Disease - pathology | Peptides - metabolism | Tauopathies - therapy | Neurons - metabolism | Parkinson Disease - metabolism | Inclusion Bodies - metabolism | Prion Diseases - therapy | Parkinson Disease - pathology | Neurodegenerative Diseases - pathology | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Alzheimer Disease - therapy | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - therapy | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Protein Folding | Trinucleotide Repeat Expansion | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Tauopathies - metabolism | Animals | Proteins - metabolism | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Mutation | Proteins - chemistry | Alzheimer Disease - genetics | Prion Diseases - metabolism | Parkinson's disease | Nervous system | Degeneration | Research | Alzheimer's disease | Proteins | Neurological disorders
Journal Article
Behavioural Brain Research, ISSN 0166-4328, 2011, Volume 221, Issue 2, pp. 564 - 573
Although Parkinson disease (PD) is viewed traditionally as a motor syndrome secondary to nigrostriatal dopaminergic denervation, recent studies emphasize... 
Dopamine | Motor | Parkinson disease with dementia | Alzheimer disease | Olfaction | Parkinson disease | Acetylcholine | Cognition | Single photon emission tomography | Positron emission tomography | Dementia with Lewy bodies | ACETYLCHOLINESTERASE ACTIVITY | ALZHEIMERS-DISEASE | MILD COGNITIVE IMPAIRMENT | NEUROSCIENCES | PEDUNCULOPONTINE NUCLEUS | ACETYLTRANSFERASE ACTIVITY | MUSCARINIC RECEPTOR SUBTYPES | IN-VIVO | HUMAN-BRAIN | BEHAVIORAL SCIENCES | PROGRESSIVE SUPRANUCLEAR PALSY | LEWY BODY DEMENTIA | Cholinergic Fibers - physiology | Lewy Body Disease - diagnosis | Humans | Neurodegenerative Diseases - diagnosis | Cholinergic Fibers - metabolism | Brain Stem - pathology | Parkinson Disease - metabolism | Neurodegenerative Diseases - diagnostic imaging | Prosencephalon - pathology | Biomarkers - metabolism | Parkinson Disease - pathology | Neurodegenerative Diseases - pathology | Parkinson Disease - diagnostic imaging | Prosencephalon - diagnostic imaging | Brain Stem - diagnostic imaging | Lewy Body Disease - pathology | Neurodegenerative Diseases - metabolism | Positron-Emission Tomography - methods | Parkinson Disease - physiopathology | Lewy Body Disease - diagnostic imaging | Cholinergic Fibers - pathology | Lewy Body Disease - metabolism | Cholinergic Fibers - diagnostic imaging | Neurodegenerative Diseases - physiopathology | Parkinson Disease - diagnosis | Models, Neurological | Lewy Body Disease - physiopathology | Parkinson's disease | Neurons | Diagnostic imaging | Alzheimer's disease | Amyloid beta-protein | motor | single photon emission tomography | cognition | olfaction | positron emission tomography | dopamine
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