New variant Creutzfeldt-Jakob disease: psychiatric features.
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Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob diseaseClinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.[A retrospective study of Creutzfeldt-Jakob disease in North of Portugal 1993-2002: demographic, clinical and neuropathological features].Rationale for diagnosing human prion disease.The relationship between new variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy.First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features.A protease-resistant prion protein isoform is present in urine of animals and humans affected with prion diseases.Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthCreutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features.New-variant Creutzfeldt-Jacob disease.Variant CJD. 18 years of research and surveillance.The transmissible spongiform encephalopathies (prion diseases): a review for dental surgeons.Neuroinflammation in Alzheimer's disease and prion disease.Cerebrospinal fluid brain-derived proteins in the diagnosis of Alzheimer's disease and Creutzfeldt-Jakob disease.Neurological and cognitive decline in adolescence.Cerebral correlates of psychotic syndromes in neurodegenerative diseasesRecent developments in the pathogenesis, diagnosis, and therapy of prion diseases.Progressive aphasia with rapidly progressive dementia in a 49 year old woman.Distinct neuropsychological characteristics in Creutzfeldt-Jakob disease.Prions impair bioaminergic functions through serotonin- or catecholamine-derived neurotoxins in neuronal cells.Genome-wide association study of behavioural and psychiatric features in human prion disease.Creutzfeldt-Jakob disease in SwedenPrion diseases as transmissible zoonotic diseases.Ethics in prion disease.Rapidly progressive young-onset dementia.Prion diseases in humans: oral and dental implications.Prion diseases: risks, characteristics, and infection control considerations in dentistry.Sporadic and Infectious Human Prion Diseases.Creutzfeldt-Jakob disease and infection control.Early identification of variant Creutzfeldt-Jakob disease.Lack of evidence to support the association of the human prion gene with schizophrenia.Neuronal and astrocytic responses involving the serotonergic system in human spongiform encephalopathies.Targeting prion amyloid deposits in vivo.Prion diseases are undercompulsory notification in Brazil: Surveillance of cases evaluated by biochemicaland/or genetic markers from 2005 to 2007.Course and causes of suspected dementia in young adults: a longitudinal study.What psychiatrists should know about sporadic Creutzfeldt-Jakob disease.
P2860
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P2860
New variant Creutzfeldt-Jakob disease: psychiatric features.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
New variant Creutzfeldt-Jakob disease: psychiatric features.
@en
type
label
New variant Creutzfeldt-Jakob disease: psychiatric features.
@en
prefLabel
New variant Creutzfeldt-Jakob disease: psychiatric features.
@en
P2093
P1433
P1476
New variant Creutzfeldt-Jakob disease: psychiatric features.
@en
P2093
A F Francis
C J Fisher
E C Johnson-Sabine
E C Johnstone
P304
P356
10.1016/S0140-6736(97)03148-6
P407
P577
1997-09-01T00:00:00Z