Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease

被引：29

作者：

Joiner, S

Linehan, J

Brandner, S

Wadsworth, JDF

Collinge, J

机构：

[1] UCL, MRC Pr Unit, London WC1N 3BG, England

[2] UCL, Dept Neurodegenerat Dis, Inst Neurol, London WC1N 3BG, England

来源：

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY | 2002年 / 73卷 / 05期

基金：

英国医学研究理事会;

关键词：

D O I：

10.1136/jnnp.73.5.597

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：597 / 598

页数：2

共 5 条

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[2] Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples [J].

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[4] Retrospective study of prion-protein accumulation in tonsil and appendix tissues [J].

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Best, D .

LANCET, 2000, 355 (9216) :1693-1694

[5] Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay [J].

Wadsworth, JDF ;

Joiner, S ;

Hill, AF ;

Campbell, TA ;

Desbruslais, M ;

Luthert, PJ ;

Collinge, J .

LANCET, 2001, 358 (9277) :171-180

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