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Free Radical Biology and Medicine, ISSN 0891-5849, 10/2013, Volume 63, pp. 1 - 29
Neurodegenerative disorders are debilitating diseases of the brain, characterized by behavioral, motor and cognitive impairments. Ample evidence underpins... 
Sirtuins | Charcot-Marie-Tooth disease and Friedreich’s ataxia | Mitochondrial dysfunction | Free radicals | Alzheimer’s disease | Neurodegenerative diseases | Amyotrophic lateral sclerosis | Co-Q10 | Huntington’s disease | PGC-1α | Creatine | Parkinson’s disease | Charcot-Marie-Tooth disease and | Parkinson's disease | Huntington's disease | Friedreich's ataxia | Alzheimer's disease | KETOGLUTARATE DEHYDROGENASE COMPLEX | PGC-1 alpha | BIOCHEMISTRY & MOLECULAR BIOLOGY | EARLY PARKINSON-DISEASE | NEURONAL CELL-DEATH | AMYOTROPHIC-LATERAL-SCLEROSIS | AMYLOID PRECURSOR PROTEIN | Charcot-Marie-Tooth disease and Friedreich's ataxia | CYTOCHROME-C-OXIDASE | TARGETED ANTIOXIDANT MITOQ | ENDOCRINOLOGY & METABOLISM | PLACEBO-CONTROLLED TRIAL | TRANSGENIC MOUSE MODEL | COMPLEX-I DEFICIENCY | Mitochondrial Diseases - pathology | Friedreich Ataxia - metabolism | Parkinson Disease - pathology | Free Radicals - toxicity | Friedreich Ataxia - pathology | Humans | Huntington Disease - pathology | Nerve Degeneration - physiopathology | Mitochondria - metabolism | Mitochondria - pathology | Charcot-Marie-Tooth Disease - pathology | Huntington Disease - metabolism | Nerve Degeneration - metabolism | Alzheimer Disease - pathology | Brain - metabolism | Amyotrophic Lateral Sclerosis - pathology | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Brain - pathology | Parkinson Disease - metabolism | Charcot-Marie-Tooth Disease - metabolism | Proteins | Nervous system diseases | Mitochondrial DNA | Gene mutations | Analysis | Index Medicus
Journal Article
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
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
Journal Article
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
Journal Article