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Science (American Association for the Advancement of Science), ISSN 1095-9203, 2002, Volume 296, Issue 5575, pp. 1991 - 1995
...Neurodegenerative disorders as diverse as Alzheimer's disease, Parkinson's disease, priori diseases, Huntington's disease, frontotemporal dementia, and motor... 
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
Journal Article
Journal Article
Journal of Alzheimer's disease, ISSN 1387-2877, 2008, Volume 15, Issue 3, pp. 473 - 493
Journal Article
Journal Article
International journal of molecular sciences, ISSN 1422-0067, 2015, Volume 16, Issue 11, pp. 26797 - 26812
.... Recent studies have suggested that impairments of the autophagic process are associated with several neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, Huntington's disease... 
Alzheimer’s disease | ALS | Huntington’s disease | SENDA | Mitophagy | Autophagy | Parkinson’s disease | autophagy | Parkinson's disease | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SELECTIVE MACROAUTOPHAGY | FRONTOTEMPORAL DEMENTIA | AMYOTROPHIC-LATERAL-SCLEROSIS | Huntington's disease | CHEMISTRY, MULTIDISCIPLINARY | CELL-DEATH | RECESSIVE JUVENILE PARKINSONISM | mitophagy | LYSOSOME FUSION | ENDOPLASMIC-RETICULUM | SIGMA-1 RECEPTOR | Alzheimer's disease | HUNTINGTONS-DISEASE | Neurons - pathology | AMP-Activated Protein Kinases - metabolism | TOR Serine-Threonine Kinases - metabolism | Humans | Huntington Disease - pathology | Multiprotein Complexes - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Alzheimer Disease - pathology | Autophagy-Related Protein-1 Homolog | Mechanistic Target of Rapamycin Complex 1 | Multiprotein Complexes - metabolism | Lysosomes - metabolism | TOR Serine-Threonine Kinases - genetics | Apoptosis Regulatory Proteins - genetics | Membrane Proteins - metabolism | Neurons - metabolism | Parkinson Disease - metabolism | Autophagy - genetics | Intracellular Signaling Peptides and Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Beclin-1 | Parkinson Disease - pathology | Signal Transduction | Membrane Proteins - genetics | Amyotrophic Lateral Sclerosis - genetics | Gene Expression Regulation | Protein-Serine-Threonine Kinases - genetics | Parkinson Disease - genetics | Huntington Disease - metabolism | Apoptosis Regulatory Proteins - metabolism | Amyotrophic Lateral Sclerosis - pathology | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Huntington Disease - genetics | Alzheimer Disease - genetics | AMP-Activated Protein Kinases - genetics | Biodegradation | Disease | Neurodegeneration
Journal Article
Journal of the neurological sciences, ISSN 0022-510X, 2012, Volume 323, Issue 1-2, 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 sclerosis, Huntington's disease and motor neuron disease... 
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 | PIRIFORM CORTEX | MOTOR-NEURON DISEASE | TIME-COURSE | REGIONAL BRAIN RESPONSES | NEUROSCIENCES | CLINICAL NEUROLOGY | MULTIPLE-SCLEROSIS | 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
Annual review of neuroscience, ISSN 1545-4126, 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... 
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