Peripheral neuropathy in Creutzfeldt-Jakob disease

被引：18

作者：

Esiri, MM

Gordon, WI

Collinge, J

Patten, JS

机构：

[1] KING EDWARD VII HOSP,DEPT NEUROL,MIDHURST,SURREY,ENGLAND

[2] KING EDWARD VII HOSP,DEPT HISTOPATHOL,MIDHURST,SURREY,ENGLAND

[3] ST MARYS HOSP,SCH MED,LONDON,ENGLAND

来源：

NEUROLOGY | 1997年 / 48卷 / 03期

关键词：

D O I：

10.1212/WNL.48.3.784

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：784 / 784

页数：1

共 4 条

[1] Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene [J].

Antoine, JC ;

Laplanche, JL ;

Mosnier, JF ;

Beaudry, P ;

Chatelain, J ;

Michel, D .

NEUROLOGY, 1996, 46 (04) :1123-1127

[2]

NEUFELD MY, 1992, MUSCLE NERVE, V15, P34

[3] DEGENERATION OF SKELETAL-MUSCLE, PERIPHERAL-NERVES, AND THE CENTRAL-NERVOUS-SYSTEM IN TRANSGENIC MICE OVEREXPRESSING WILD-TYPE PRION PROTEINS [J].

WESTAWAY, D ;

DEARMOND, SJ ;

CAYETANOCANLAS, J ;

GROTH, D ;

FOSTER, D ;

YANG, SL ;

TORCHIA, M ;

CARLSON, GA ;

PRUSINER, SB .

CELL, 1994, 76 (01) :117-129

[4] A new variant of Creutzfeldt-Jakob disease in the UK [J].

Will, RG ;

Ironside, JW ;

Zeidler, M ;

Cousens, SN ;

Estibeiro, K ;

Alperovitch, A ;

Poser, S ;

Pocchiari, M ;

Hofman, A ;

Smith, PG .

LANCET, 1996, 347 (9006) :921-925

← 1 →