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Rapidly Progressive DementiaRapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Fulminant corticobasal degeneration: Agrypnia excitata in corticobasal syndrome.Complex proteinopathy with accumulations of prion protein, hyperphosphorylated tau, α-synuclein and ubiquitin in experimental bovine spongiform encephalopathy of monkeys.Rapidly progressive diffuse Lewy body disease.Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob diseasePredicting aggressive decline in mild cognitive impairment: the importance of white matter hyperintensitiesCerebrospinal fluid markers in sporadic Creutzfeldt-Jakob diseaseRapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease.Comparative Incidence of Conformational, Neurodegenerative Disorders.Rapidly progressive dementias and the treatment of human prion diseases.The evaluation of rapidly progressive dementia.Rates of brain atrophy and clinical decline over 6 and 12-month intervals in PSP: determining sample size for treatment trials.Clinically Unsuspected Prion Disease Among Patients With Dementia Diagnoses in an Alzheimer's Disease Database.Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 yearsCriteria for the diagnosis of corticobasal degenerationRapidly progressive dementia and ataxia in an elderly manPredicting Survival in Dementia With Lewy Bodies With Hippocampal VolumetryUpdated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.Dementia with Lewy Bodies: Molecular Pathology in the Frontal Cortex in Typical and Rapidly Progressive Forms.Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels.Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia can present as frontotemporal dementia syndrome.Cognitive impairment and vitamin B12: a review.Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases.Sensitivity to biases of case-control studies on medical procedures, particularly surgery and blood transfusion, and risk of Creutzfeldt-Jakob disease.When dementia progresses quickly: a practical approach to the diagnosis and management of rapidly progressive dementia.Corticobasal syndrome due to sporadic Creutzfeldt-Jakob disease: a review and neuropsychological case report.Survival and Causes of Death Among People With Clinically Diagnosed Synucleinopathies With Parkinsonism: A Population-Based Study.Dementia and Rapid Mortality: Who is at Risk?Spectrum of noncerebrovascular rapidly progressive cognitive deterioration: a 2-year retrospective study.Unusual features of Creutzfeldt-Jakob disease followed-up in a memory clinic.Pellagra encephalopathy as a differential diagnosis for Creutzfeldt-Jakob disease.Cerebrovascular lesions in patients with frontotemporal lobar degeneration: a neuropathological study.
P2860
Q28071290-D9EE147B-03A4-4919-B447-06E831FE20FCQ30446918-0BC184DD-3304-4A40-87EF-1A9B66D11CA6Q30736825-AE4ADF3B-7120-423C-BCCA-A3E108AE2998Q33761828-BB992D28-233C-4C17-ABA6-B2F7ED15A011Q33870090-0218D84B-B34A-4F13-9B69-C646AA5D021DQ33933305-A864A359-E18B-4E35-A826-5685A3CF5178Q33938347-F31A8DAD-34B3-47F4-A2CF-6661AFD99B67Q35297556-DED4CBA0-8920-4898-BAFC-6DCDD13E7056Q35667410-1517DAB0-9890-4858-969C-BA88637C214FQ35763399-BAD940AB-B878-40E5-982F-D29C008A30E2Q35832931-99576830-3E98-4ECF-A221-7F0361D23962Q35974573-FC48383F-E624-4487-A609-BFAFD9CEEC5CQ36101560-5E01CDD2-4A5C-483D-B460-A108B10446C1Q36296509-CBD52658-61EE-4378-88B9-4E95D9BB3DA6Q36315347-D136608F-120A-4529-A811-C3DEBA4FDA27Q36661843-6A53C7A3-21E7-4D50-ABA4-EDF95DB64F96Q36876642-CFCE2296-E193-442B-B9DF-ED20A20376CEQ37062727-75C4591D-8243-4FD4-B3D9-539CF456C790Q37381059-A93689F1-FA6C-48C5-9438-CFBC5CB0CC36Q37694473-64A70CB0-DBB4-4D12-B01B-F7A8E1C01464Q37697455-05DDBE84-85BA-4F4A-B4C0-8ED8233FA5F0Q37943968-7B1E26AB-4198-43AF-B0DD-F269E9CA6E78Q37973493-FE280B1F-DA78-4A19-9169-EA8AC7CD0319Q38006910-27CFBD5C-2786-4D23-B0FC-D7C8EE0DD5D8Q38025005-4ECA56F7-5315-4DED-B353-E21DBB5C660CQ38196861-08833792-88AD-4706-9E34-87BFAE139A39Q39015633-68E5638C-F312-4D5F-92C3-5F95BA34DCF9Q40201095-2B0C78F6-2847-44C9-B391-9D3AE5C18B2BQ40786223-CD8D5AA7-8B00-4AE5-8E32-C56E0CF09A43Q45916641-4C20F833-5A3F-4F81-B07A-7B8CC0175429Q48361950-D7319C99-2E8D-4459-B0A7-CBECD26E72E0Q48548307-E51CD29A-7563-49C7-8A28-EC653083C1A0Q48635620-5898384A-4D7C-431C-9505-B42356F73FAD
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Rapidly progressive neurodegenerative dementias.
@en
Rapidly progressive neurodegenerative dementias.
@nl
type
label
Rapidly progressive neurodegenerative dementias.
@en
Rapidly progressive neurodegenerative dementias.
@nl
prefLabel
Rapidly progressive neurodegenerative dementias.
@en
Rapidly progressive neurodegenerative dementias.
@nl
P2093
P2860
P1433
P1476
Rapidly progressive neurodegenerative dementias.
@en
P2093
Bradley F Boeve
Brian A Crum
Caterina Giannini
Joseph E Parisi
Keith A Josephs
P2860
P304
P356
10.1001/ARCHNEUROL.2008.534
P577
2009-02-01T00:00:00Z