The nosology and neuropathology of human conditions related to unconventional infectious agents or prions

被引：11

作者：

Hauw, JJ

Sazdovitch, V

Seilhean, D

Camilleri, S

Lazarini, F

DelasnerieLaupretre, N

Duyckaerts, C

机构：

[1] R. Escourolle Neuropathology Lab., Salpêtrière Hospital, Paris VI University, 75651, Paris Cedex 13

来源：

EUROPEAN JOURNAL OF NEUROLOGY | 1996年 / 3卷 / 06期

关键词：

human spongiform encephalopathies; slow virus diseases; prion diseases; Creutzfeldt-Jakob disease; neuropathology;

D O I：

10.1111/j.1468-1331.1996.tb00263.x

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：487 / 499

页数：13

共 127 条

[1] THE APOLIPOPROTEIN-E ALLELES AS MAJOR SUSCEPTIBILITY FACTORS FOR CREUTZFELDT-JAKOB-DISEASE [J].

AMOUYEL, P ;

VIDAL, O ;

LAUNAY, JM ;

LAPLANCHE, JL .

LANCET, 1994, 344 (8933) :1315-1318

[2]

ANDERSON R, 1971, 6 C INT NEUR PAR MAS

[3] MICROGLIA IS A COMPONENT OF THE PRION PROTEIN AMYLOID PLAQUE IN THE GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME [J].

BARCIKOWSKA, M ;

LIBERSKI, PP ;

BOELLAARD, JW ;

BROWN, P ;

GAJDUSEK, DC ;

BUDKA, H .

ACTA NEUROPATHOLOGICA, 1993, 85 (06) :623-627

[4] EXPERIMENTAL KURU IN SPIDER MONKEY - HISTOPATHOLOGICAL AND ULTRASTRUCTURAL STUDIES OF BRAIN DURING EARLY STAGES OF INCUBATION [J].

BECK, E ;

BAK, IJ ;

CHRIST, JF ;

GAJDUSEK, DC ;

GIBBS, CJ ;

HASSLER, R .

BRAIN, 1975, 98 (DEC) :595-&

[5]

BECK E, 1971, 6 C INT NEUR PAR MAS

[6] SUB-ACUTE SPONGIFORM ENCEPHALOPATHY WITH MULTIFORM PLAQUE-FORMATION - PECULIAR FAMILIAL HEREDITARY-DISEASE OF CNS [SPINOCEREBELLAR ATROPHY WITH DEMENTIA, PLAQUES, AND PLAQUE-LIKE DEPOSITS IN CEREBELLUM AND CEREBRUM (GERSTMANN, STRAUSSLER, SCHEINKER)] [J].

BOELLAARD, JW ;

SCHLOTE, W .

ACTA NEUROPATHOLOGICA, 1980, 49 (03) :205-212

[7]

BRION J, 1987, NEUROSCI LETT, V78, P115

[8]

BRION S, 1993, REV NEUROL, V149, P815

[9]

BRION S, 1983, VIRUS NON CONVENTION, P227

[10]

BROSWNELL B, 1965, J NEUROL NEUROSUR PS, V37, P195

← 1 2 3 4 5 6 7 8 9 10 →