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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
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
2002, 3rd ed., Oxford monographs on medical genetics, ISBN 0198510608, Volume 45, xvi, 558
Book
2017, Handbook of clinical neurology, ISBN 0128018933, Volume 144, 3rd Series
Web Resource
2017, Handbook of clinical neurology, ISBN 0128018933, Volume 144, 3rd Series
Web Resource
Journal of the Neurological Sciences, ISSN 0022-510X, 2012, Volume 323, Issue 1, pp. 16 - 24
Abstract It is known that the olfactory dysfunction is involved in various neurological diseases, such as Parkinson's disease, Alzheimer's disease, multiple... 
Neurology | Multiple sclerosis | Parkinson's disease | Olfactory dysfunction | Motor neuron disease | Functional magnetic resonance imaging | Huntington's disease | Olfactory event-related potentials | Alzheimer's disease | ALZHEIMERS-DISEASE | ENSHEATHING CELLS | MOTOR-NEURON DISEASE | MILD COGNITIVE IMPAIRMENT | REGIONAL BRAIN RESPONSES | NEUROSCIENCES | CLINICAL NEUROLOGY | MULTIPLE-SCLEROSIS | HUNTINGTONS-DISEASE | ODOR IDENTIFICATION | OF-PENNSYLVANIA SMELL | PARKINSONS-DISEASE | Parkinson Disease - complications | Alzheimer Disease - physiopathology | Alzheimer Disease - complications | Motor Neuron Disease - complications | Sensory Thresholds | Humans | Evoked Potentials | Olfaction Disorders - diagnosis | Parkinson Disease - physiopathology | Neurodegenerative Diseases - complications | Odorants | Huntington Disease - complications | Multiple Sclerosis - complications | Neuropsychological Tests | Olfactory Pathways - physiopathology | Magnetic Resonance Imaging | Multiple Sclerosis - physiopathology | Neurodegenerative Diseases - physiopathology | Aging - physiology | Discrimination (Psychology) | Olfaction Disorders - physiopathology | Motor Neuron Disease - physiopathology | Olfaction Disorders - etiology | Huntington Disease - physiopathology | Nervous system diseases | Diagnostic imaging | Huntington's chorea
Journal Article