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2002, 3rd ed., Oxford monographs on medical genetics, ISBN 0198510608, Volume no. 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
1981, ISBN 0387105883, xvii, 192
Book
European Journal of Neurology, ISSN 1351-5101, 2012, Volume 19, Issue 9, pp. 1159 - 1179
Click here for the corresponding questions to this CME article. 
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
1999, Oxford medical publications., ISBN 9780192629302, xviii, 139
Book
1989, ISBN 0801838606, x, 251
Book
1993, ISBN 0521459834, Volume 23., 46
This report presents the findings of a study of people affected by Huntington's chorea and their unaffected relatives, and in particular, of the incidence of... 
Book
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 4, pp. e19338 - e19338
Journal Article
2011, RSC drug discovery series, ISBN 9781849731843, Volume no. 6., xv, 290
"In recent years, medical developments have resulted in an increase in human life expectancy. Some developed countries now have a larger population of... 
Neurodegenerative Diseases | Nervous system | physiopathology | Animal models | Degeneration | Disease Models, Animal | Chemistry | Parkinson's disease | Animal models in research | Huntington's disease | Alzheimer's disease
Book
2011, Frontiers in neuroscience, ISBN 0849390001, xx, 312
In 1993, the genetic mutation responsible for Huntington’s disease (HD) was identified. Considered a milestone in human genomics, this discovery has led to... 
Huntington Disease | physiopathology | drug therapy | Molelcular aspects | Pathophysiology | methods | Neuropharmacology | Huntington's disease | Drug Discovery | Biotechnology | Neuroscience
Book