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Tag Archives: University of Oxford: Radcliffe Department of Medicine
Generic Protocol(s) for Diagnostic Test Accuracy Reviews in Dementia (Cochrane Database)
Summary The Cochrane Dementia and Cognitive Improvement Group (CDCIG) is working – in collaboration with the Cochrane Diagnostic Test Accuracy Review Unit (DTA Unit) and the Institute of Public Health (IPH) – on a series of Cochrane Diagnostic Test Accuracy … Continue reading →
Posted in Diagnosis, For Doctors (mostly), For Researchers (mostly), International, NIHR, Systematic Reviews, UK
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Tagged 6-Item Cognitive Impairment Test (6-CIT), Abbreviated Mental Test (AMT), Addenbrooke's Cognitive Exaination-Revised (ACE-R), ALOIS: the Cochrane Dementia and Cognitive Improvement Group, APOE e4 (Apolipoprotein E e4), Asymptomatic Alzheimer’s Disease, Avon and Wiltshire Mental Health Partnership NHS Trust, Blessed Information-Memory-Concentration Test (Blessed I-M-C), Bristol, Bristol University: Academic Unit of Psychiatry, Bristol University: Addiction and Suicide Research, Bristol University: Centre for Mental Health, Bristol University: School of Community Medicine, CDCIG: Cochrane Dementia and Cognitive Improvement Group, Clock Drawing Test (CDT), Cochrane Dementia and Cognitive Improvement Group (CDCIG), Cochrane Dementia and Cognitive Improvement Group: Oxford University, Cochrane Diagnostic Test Accuracy (DTA) Dementia Reviews, Cochrane Diagnostic Test Accuracy (DTA) Reviews, Cochrane Diagnostic Test Accuracy Review Unit (DTA Unit), Cognitive Assessments / Screening Tools, CSF (Cerebrospinal Fluid Analysis of Amyloid Beta and Tau), Diagnostic Test Accuracy (DTA) Handbook, Diagnostic Test Accuracy Reviews, DTA Handbook, Exeter, FP-CIT (Fluoropropyl-Carbomethoxy-3b-(4-Iodophenyl)Tropane), Generic Protocols for Cross-Sectional and Delayed-Verification Studies, Glasgow, GP-Cog, Institute of Public Health (IPH), Institute of Public Health: Cambridge, Mini Mental State Examination (MMSE), Mini-Cog, Modified Mini-Mental State Examination (3-MS), Montreal Cognitive Assessment (MoCA), National Institute for Health Research (NIHR) Cochrane Collaboration Programme, Neuropsychological Tests for Alzheimer’s Disease Diagnosis, Neuropsychological Tests for Dementia Diagnosis, Oxford, Peninsula Technology Assessment Group (PenTAG), PET-FDG (Positron Emission Tomography F-Fluorodeoxyglucose), PET-PiB (Positron Emission Tomography-Pittsburgh Compound B), Protocols, Research Protocol, School of Community Medicine: Bristol University, School of Social and Community Medicine: Bristol University, Severn Deanery (Bristol UK), sMRI (Structural Magnetic Resonance Imaging), SPECT (Single Photon Emission Computed Tomography), St Louis University Mental Status Examination (SLUMS), Study Protocol, Systematic Reviews and Meta-Analyses, Test Your Memory (TYM), University of Bristol, University of Bristol: School of Social and Community Medicine, University of Cambridge, University of Cambridge: Department of Public Health and Primary Care: Cambridge, University of Exeter, University of Exeter Medical School, University of Glasgow, University of Oxford, University of Oxford: Radcliffe Department of Medicine
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Concerning the Diagnostic Accuracy of Plasma and CSF Biomarkers (Cochrane Database)
Summary This systematic review investigates the diagnostic accuracy of blood plasma and CSF Aß levels for detecting patients with mild cognitive impairment (MCI) and who are likely to progress to Alzheimer’s Disease or other types of dementia. The accuracy of … Continue reading →
Posted in Charitable Bodies, Diagnosis, For Doctors (mostly), For Researchers (mostly), International, Systematic Reviews, UK
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Tagged Aß40, Aß42, ALOIS: the Cochrane Dementia and Cognitive Improvement Group, Alzheimer's Association, Alzheimer's Disease and Related Disorders Association (Now the Alzheimer's Association), Alzheimer’s Disease Biomarkers, Amyloid, Amyloid Beta, Amyloid Beta Protein, Amyloid Proteins, Amyloid-β (Aβ), Apolipoprotein E, Asymptomatic Alzheimer’s Disease, Beta-Amyloid, Beta-Amyloid Plaques, Biomarker Assessments in Alzheimer’s Disease, Biomarker Assessments in Alzheimer’s Disease Clinical Trials, Biomarkers, Biomarkers Predicting Cognitive Decline and Alzheimer's Disease, Blood-Based Biomarkers, Cambridge Institute of Public Health, Cambridge Institute of Public Health: Cambridge University, Candidate Blood Proteome Markers, Cerebrospinal Fluid, Cerebrospinal Fluid (CSF), Cerebrospinal Fluid (CSF) Biomarkers, Cochrane Database, Cochrane Database of Systematic Reviews, Cochrane Dementia and Cognitive Improvement Group, Cochrane Register of Diagnostic Test Accuracy Studies, Cognitive Impairment, Cognitive Response to Progression of Pathophysiology, Conversion to Dementia From Prodromal Disease, CSF Aß Levels, CSF Aβ, CSF Biomarkers, CSF Tau, Dementia Screening, Diagnostic and Statistical Manual of Mental Disorders Fourth Edition (DSM-IV), Diagnostic Test Accuracy, Early Detection of Alzheimer’s Disease, Early Detection of Preclinical Disease, Early Diagnosis, Early Diagnosis of Alzheimer's Disease, Early Differential Diagnosis, Early Screening, Fluid and Imaging Biomarkers, Imperial College London, Institute of Public Health: University of Cambridge, β-amyloid, β-Amyloid 1-42 (Aβ42), MCI: Mild Cognitive Impairment, Mild Cognitive Impairment (MCI), National Institute of Neurological and Communicative Disorders and Stroke, Neurodegeneration, NINCDS-ADRDA Criteria, NINCDS-ADRDA: National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer Disease and Related Disorders Association, Plasma Biomarkers, Plasma Proteins, Preclinical Alzheimer's Disease, Prodromal Alzheimer's Disease, Progression of Mild Cognitive Impairment to Dementia, Systematic Reviews and Meta-Analyses, Transition from Cognitive Impairment to Dementia, University of Birmingham, University of Cambridge, University of Oxford, University of Oxford: Radcliffe Department of Medicine, University of Western Australia, US Alzheimer's Association, Western Australian Centre for Health and Ageing (WACHA)
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