A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features
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Rapidly progressive dementia due to Mycobacterium neoaurum meningoencephalitisPrion DiseasesDifferential diagnosis of Jakob-Creutzfeldt disease[A retrospective study of Creutzfeldt-Jakob disease in North of Portugal 1993-2002: demographic, clinical and neuropathological features].Sporadic Creutzfeldt-Jakob disease with cerebellar ataxia at onset in the UKThe expanding universe of prion diseases.Geographical distribution of cases of Creutzfeldt-Jakob disease in England and Wales 1970-84A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979. II: Epidemiology.Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors.A case of Creutzfeldt-Jakob disease presenting with cortical deafnessExtent of misclassification of death from Creutzfeldt-Jakob disease in England 1979-96: retrospective examination of clinical recordsCreutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features.The transmissible spongiform encephalopathies (prion diseases): a review for dental surgeons.Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob diseaseDistinct neuropsychological characteristics in Creutzfeldt-Jakob disease.Neuroimaging findings in human prion disease.Creutzfeldt-Jakob disease in the elderly.Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease.Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory FindingsHow to tackle a possible Creutzfeldt-Jakob disease necropsyCase series of probable sporadic Creutzfeldt-Jakob disease from Eastern India.Mortality from dementia in occupations at risk of exposure to bovine spongiform encephalopathy: analysis of death registrationsSporadic Creutzfeldt-Jacob Disease: An 8-Year Experience from a Single Center in Turkey.Other dementias.Imaging of prion diseases.Sporadic Creutzfeldt-Jakob disease (sCJD) with asymmetric findingsA clinicopathological approach to the diagnosis of dementia.Creutzfeldt-Jakob disease presenting with visual symptoms: a case of the 'Heidenhain variant'.Lack of evidence to support the association of the human prion gene with schizophrenia.Prion diseases are undercompulsory notification in Brazil: Surveillance of cases evaluated by biochemicaland/or genetic markers from 2005 to 2007.Rare case of atypical parkinsonism: why family history is important.Unusual features of Creutzfeldt-Jakob disease followed-up in a memory clinic.Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease.What psychiatrists should know about sporadic Creutzfeldt-Jakob disease.Serum tau protein as a marker for the diagnosis of Creutzfeldt-Jakob disease.Guidelines for Drug Trials in the Treatment of Age-Associated Cognitive Decline and Alzheimer's Disease
P2860
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P2860
A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features
description
1984 nî lūn-bûn
@nan
1984 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
A retrospective study of Creut ...... 1970-79. I: Clinical features
@ast
A retrospective study of Creut ...... 1970-79. I: Clinical features
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type
label
A retrospective study of Creut ...... 1970-79. I: Clinical features
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A retrospective study of Creut ...... 1970-79. I: Clinical features
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prefLabel
A retrospective study of Creut ...... 1970-79. I: Clinical features
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A retrospective study of Creut ...... 1970-79. I: Clinical features
@en
P2860
P356
P1476
A retrospective study of Creut ...... 1970-79. I: Clinical features
@en
P2093
P2860
P304
P356
10.1136/JNNP.47.2.134
P407
P577
1984-02-01T00:00:00Z