IMMUNOCHEMICAL, MOLECULAR GENETIC, AND TRANSMISSION STUDIES ON A CASE OF GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME

被引：93

作者：

TATEISHI, J

KITAMOTO, T

DOHURA, K

SAKAKI, Y

STEINMETZ, G

TRANCHANT, C

WARTER, JM

HELDT, N

机构：

[1] KYUSHU UNIV,GENET INFORMAT LAB,FUKUOKA 812,JAPAN

[2] UNIV STRASBOURG 1,HOP HAUTEPIERRE,FAC MED,SERV ANAT PATHOL,F-67070 STRASBOURG,FRANCE

来源：

NEUROLOGY | 1990年 / 40卷 / 10期

关键词：

D O I：

10.1212/WNL.40.10.1578

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：1578 / 1581

页数：4

共 32 条

[1] EXPERIMENTAL TRANSMISSION OF AN AUTOSOMAL DOMINANT SPONGIFORM ENCEPHALOPATHY - DOES THE INFECTIOUS AGENT ORIGINATE IN THE HUMAN GENOME [J].

BAKER, HF ;

RIDLEY, RM ;

CROW, TJ .

BRITISH MEDICAL JOURNAL, 1985, 291 (6491) :299-302

[2] CREUTZFELDT-JAKOB DISEASE PRION PROTEINS IN HUMAN BRAINS [J].

BOCKMAN, JM ;

KINGSBURY, DT ;

MCKINLEY, MP ;

BENDHEIM, PE ;

PRUSINER, SB .

NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (02) :73-78

[3] DIAGNOSIS OF CREUTZFELDT-JAKOB DISEASE BY WESTERN-BLOT IDENTIFICATION OF MARKER PROTEIN IN HUMAN-BRAIN TISSUE [J].

BROWN, P ;

COKERVANN, M ;

POMEROY, K ;

FRANKO, M ;

ASHER, DM ;

GIBBS, CJ ;

GAJDUSEK, DC .

NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (09) :547-551

[4] LINKAGE OF PRION PROTEIN AND SCRAPIE INCUBATION-TIME GENES [J].

CARLSON, GA ;

KINGSBURY, DT ;

GOODMAN, PA ;

COLEMAN, S ;

MARSHALL, ST ;

DEARMOND, S ;

WESTAWAY, D ;

PRUSINER, SB .

CELL, 1986, 46 (04) :503-511

[5] DIAGNOSIS OF GERSTMANN-STRAUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS [J].

COLLINGE, J ;

HARDING, AE ;

OWEN, F ;

POULTER, M ;

LOFTHOUSE, R ;

BOUGHEY, AM ;

SHAH, T ;

CROW, TJ .

LANCET, 1989, 2 (8653) :15-17

[6] IDENTIFICATION OF A GENE WHICH CONTROLS INCUBATION PERIOD OF SOME STRAINS OF SCRAPIE AGENT IN MICE [J].

DICKINSON, AG ;

MEIKLE, VMH ;

FRASER, H .

JOURNAL OF COMPARATIVE PATHOLOGY, 1968, 78 (03) :293-+

[7] PRO-]LEU CHANGE AT POSITION-102 OF PRION PROTEIN IS THE MOST COMMON BUT NOT THE SOLE MUTATION RELATED TO GERSTMANN-STRAUSSLER SYNDROME [J].

DOHURA, K ;

TATEISHI, J ;

SASAKI, H ;

KITAMOTO, T ;

SAKAKI, Y .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) :974-979

[8] CREUTZFELDT-JAKOB DISEASE PATIENTS WITH CONGOPHILIC KURU PLAQUES HAVE THE MISSENSE VARIANT PRION PROTEIN COMMON TO GERSTMANN-STRAUSSLER SYNDROME [J].

DOHURA, K ;

TATEISHI, J ;

KITAMOTO, T ;

SASAKI, H ;

SAKAKI, Y .

ANNALS OF NEUROLOGY, 1990, 27 (02) :121-126

[9] GERSTMANN-STRAUSSLER-SCHEINKER DISEASE .1. EXTENDING THE CLINICAL SPECTRUM [J].

FARLOW, MR ;

YEE, RD ;

DLOUHY, SR ;

CONNEALLY, PM ;

AZZARELLI, B ;

GHETTI, B .

NEUROLOGY, 1989, 39 (11) :1446-1452

[10]

Gerstmann J., 1936, Z NEUROL, V154, P736, DOI DOI 10.1007/BF02865827

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