Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968--1977.
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Sporadic Creutzfeldt-Jakob disease with cerebellar ataxia at onset in the UK14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients.Rapidly progressive dementia caused by spongiform encephalopathy.A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical featuresCreutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features.Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant".Molecular pathogenesis of sporadic prion diseases in man.Creutzfeldt-Jakob disease in SwedenSporadic Creutzfeldt-Jakob disease (sCJD) with asymmetric findingsA new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.Lack of evidence to support the association of the human prion gene with schizophrenia.Alzheimer's disease and transmissible virus dementia (Creutzfeldt-Jakob disease).Creutzfeldt-Jakob disease in Venezuela. A case report.Verbal perseveration as the initial symptom in a case of Creutzfeldt‐Jakob disease
P2860
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P2860
Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968--1977.
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
Creutzfeldt-Jakob disease in F ...... during the decade 1968--1977.
@en
type
label
Creutzfeldt-Jakob disease in F ...... during the decade 1968--1977.
@en
prefLabel
Creutzfeldt-Jakob disease in F ...... during the decade 1968--1977.
@en
P2093
P356
P1433
P1476
Creutzfeldt-Jakob disease in F ...... during the decade 1968--1977.
@en
P2093
P304
P356
10.1002/ANA.410060510
P577
1979-11-01T00:00:00Z