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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
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2003, Volume 302, Issue 5646, pp. 830 - 834
Early detection of neurodegenerative disorders would provide clues to the underlying pathobiology of these diseases and would enable more effective diagnosis and treatment of patients... 
Neurology | Nervous system diseases | Neurodegenerative diseases | Imaging | Huntington disease | Parkinson disease | Disease manifestations | Biological markers | Alzheimers disease | Early detection | Reviews and Viewpoints | SUBCLINICAL DOPAMINERGIC DYSFUNCTION | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | ELDERLY SUBJECTS | FRONTAL-CORTEX | FAMILY-HISTORY DATA | AMYLOID PLAQUES | E TYPE-4 ALLELE | MILD COGNITIVE IMPAIRMENT | CEREBROSPINAL-FLUID | PARKINSONS-DISEASE | Humans | Huntington Disease - pathology | Memory | Neurodegenerative Diseases - diagnosis | Alzheimer Disease - pathology | Alzheimer Disease - diagnosis | Brain - metabolism | Time Factors | Aging | Huntington Disease - diagnosis | Parkinson Disease - metabolism | Dopamine - metabolism | Genetic Predisposition to Disease | Parkinson Disease - pathology | Neurodegenerative Diseases - pathology | Biomarkers - analysis | Neurodegenerative Diseases - genetics | Genetic Markers | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Huntington Disease - metabolism | Cognition Disorders - diagnosis | Diagnostic Imaging | Alzheimer Disease - metabolism | Brain - pathology | Huntington Disease - genetics | Parkinson Disease - diagnosis | Mutation | Alzheimer Disease - genetics | Evaluation | Nervous system | Degeneration | Diagnostic services | Pathology | Molecular biology | Neurological disorders
Journal Article
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 2008, Volume 15, Issue 3, pp. 473 - 493
Journal Article
Journal Article
European journal of neurology, ISSN 1351-5101, 2012, Volume 19, Issue 9, pp. 1159 - 1179
.... In 2010, the revised guidelines for Alzheimer's disease (AD) were published. The current guidelines involve the revision of the dementia syndromes outside of AD... 
treatment | management | review | guideline | dementia | diagnosis | recommendation | Treatment | Guideline | Diagnosis | Management | Review | Recommendation | Dementia | DIFFERENTIAL-DIAGNOSIS | ALZHEIMERS-DISEASE | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | POSITRON-EMISSION-TOMOGRAPHY | VASCULAR COGNITIVE IMPAIRMENT | NORMAL-PRESSURE HYDROCEPHALUS | CREUTZFELDT-JAKOB-DISEASE | LEWY BODIES | PROGRESSIVE SUPRANUCLEAR PALSY | PARKINSONS-DISEASE | Parkinson Disease - therapy | Primary Progressive Nonfluent Aphasia - therapy | Lewy Body Disease - diagnosis | Humans | Dementia - diagnosis | Lewy Body Disease - therapy | Alzheimer Disease - diagnosis | Huntington Disease - therapy | Limbic Encephalitis - therapy | Dementia, Vascular - diagnosis | Frontotemporal Lobar Degeneration - diagnosis | Frontotemporal Lobar Degeneration - therapy | Huntington Disease - diagnosis | Dementia, Vascular - therapy | Limbic Encephalitis - diagnosis | Primary Progressive Nonfluent Aphasia - diagnosis | Prion Diseases - diagnosis | Prion Diseases - therapy | Dementia - therapy | Alzheimer Disease - therapy | Hydrocephalus, Normal Pressure - therapy | Supranuclear Palsy, Progressive - therapy | Parkinson Disease - diagnosis | Supranuclear Palsy, Progressive - diagnosis | Hydrocephalus, Normal Pressure - diagnosis | Care and treatment | Parkinson's disease | Huntington's chorea | Analysis | Practice guidelines (Medicine) | Diagnostic imaging | Alzheimer's disease | Disease | Metabolic disorders | Neuroimaging | Hydrocephalus | Neurodegenerative diseases | EEG | Cognitive ability | Cerebrospinal fluid | Huntington's disease | Blood | Genetic screening | Lewy bodies | Reviews | Dementia disorders | Frontotemporal dementia | Prion protein | Movement disorders | progressive supranuclear palsy | Index Medicus
Journal Article