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Movement Disorders (revue)

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Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease

Identifieur interne : 002629 ( PascalFrancis/Corpus ); précédent : 002628; suivant : 002630

Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease

Auteurs : Mark A. Hellmann ; Eldad Melamed

Source :

RBID : Pascal:02-0584388

Descripteurs français

English descriptors

Abstract

A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation-positive Creutzfeldt-Jakob disease.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 17
A06       @2 5
A08 01  1  ENG  @1 Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease
A11 01  1    @1 HELLMANN (Mark A.)
A11 02  1    @1 MELAMED (Eldad)
A14 01      @1 Department of Neurology, Rabin Medical Centre, Beilinson Campus and Tel Aviv University School of Medicine @2 Petah Tiqva @3 ISR @Z 1 aut. @Z 2 aut.
A20       @1 1097-1098
A21       @1 2002
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000105152380370
A44       @0 0000 @1 © 2002 INIST-CNRS. All rights reserved.
A45       @0 7 ref.
A47 01  1    @0 02-0584388
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation-positive Creutzfeldt-Jakob disease.
C02 01  X    @0 002B17G
C02 02  X    @0 235
C03 01  X  FRE  @0 Encéphalopathie spongiforme Creutzfeldt Jakob @5 01
C03 01  X  ENG  @0 Creutzfeldt Jakob disease @5 01
C03 01  X  SPA  @0 Encefalopatía espongiforme Creutzfeldt Jakob @5 01
C03 02  X  FRE  @0 Dystonie @5 04
C03 02  X  ENG  @0 Dystonia @5 04
C03 02  X  SPA  @0 Distonía @5 04
C03 03  X  FRE  @0 Lésion focale @5 07
C03 03  X  ENG  @0 Focal lesion @5 07
C03 03  X  SPA  @0 Lesión focal @5 07
C03 04  X  FRE  @0 Etude cas @5 16
C03 04  X  ENG  @0 Case study @5 16
C03 04  X  SPA  @0 Estudio caso @5 16
C03 05  X  FRE  @0 Signe inaugural @5 17
C03 05  X  ENG  @0 Inaugural sign @5 17
C03 05  X  SPA  @0 Signo inaugural @5 17
C03 06  X  FRE  @0 Homme @5 20
C03 06  X  ENG  @0 Human @5 20
C03 06  X  SPA  @0 Hombre @5 20
C03 07  X  FRE  @0 Prion @5 25
C03 07  X  ENG  @0 Prion @5 25
C03 07  X  SPA  @0 Prión @5 25
C07 01  X  FRE  @0 Infection
C07 01  X  ENG  @0 Infection
C07 01  X  SPA  @0 Infección
C07 02  X  FRE  @0 Système nerveux pathologie @5 37
C07 02  X  ENG  @0 Nervous system diseases @5 37
C07 02  X  SPA  @0 Sistema nervioso patología @5 37
C07 03  X  FRE  @0 Système nerveux central pathologie @5 38
C07 03  X  ENG  @0 Central nervous system disease @5 38
C07 03  X  SPA  @0 Sistema nervosio central patología @5 38
C07 04  X  FRE  @0 Encéphale pathologie @5 39
C07 04  X  ENG  @0 Cerebral disorder @5 39
C07 04  X  SPA  @0 Encéfalo patología @5 39
C07 05  X  FRE  @0 Maladie dégénérative @5 40
C07 05  X  ENG  @0 Degenerative disease @5 40
C07 05  X  SPA  @0 Enfermedad degenerativa @5 40
C07 06  X  FRE  @0 Muscle strié pathologie @5 45
C07 06  X  ENG  @0 Striated muscle disease @5 45
C07 06  X  SPA  @0 Músculo estriado patología @5 45
C07 07  X  FRE  @0 Trouble neurologique @5 47
C07 07  X  ENG  @0 Neurological disorder @5 47
C07 07  X  SPA  @0 Trastorno neurológico @5 47
C07 08  X  FRE  @0 Mouvement involontaire @5 48
C07 08  X  ENG  @0 Involuntary movement @5 48
C07 08  X  SPA  @0 Movimiento involuntario @5 48
C07 09  X  FRE  @0 Extrapyramidal syndrome @5 49
C07 09  X  ENG  @0 Extrapyramidal syndrome @5 49
C07 09  X  SPA  @0 Extrapiramidal síndrome @5 49
N21       @1 343
N82       @1 PSI

Format Inist (serveur)

NO : PASCAL 02-0584388 INIST
ET : Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease
AU : HELLMANN (Mark A.); MELAMED (Eldad)
AF : Department of Neurology, Rabin Medical Centre, Beilinson Campus and Tel Aviv University School of Medicine/Petah Tiqva/Israël (1 aut., 2 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2002; Vol. 17; No. 5; Pp. 1097-1098; Bibl. 7 ref.
LA : Anglais
EA : A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation-positive Creutzfeldt-Jakob disease.
CC : 002B17G; 235
FD : Encéphalopathie spongiforme Creutzfeldt Jakob; Dystonie; Lésion focale; Etude cas; Signe inaugural; Homme; Prion
FG : Infection; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Maladie dégénérative; Muscle strié pathologie; Trouble neurologique; Mouvement involontaire; Extrapyramidal syndrome
ED : Creutzfeldt Jakob disease; Dystonia; Focal lesion; Case study; Inaugural sign; Human; Prion
EG : Infection; Nervous system diseases; Central nervous system disease; Cerebral disorder; Degenerative disease; Striated muscle disease; Neurological disorder; Involuntary movement; Extrapyramidal syndrome
SD : Encefalopatía espongiforme Creutzfeldt Jakob; Distonía; Lesión focal; Estudio caso; Signo inaugural; Hombre; Prión
LO : INIST-20953.354000105152380370
ID : 02-0584388

Links to Exploration step

Pascal:02-0584388

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   |area=    MovDisordV3
   |flux=    PascalFrancis
   |étape=   Corpus
   |type=    RBID
   |clé=     Pascal:02-0584388
   |texte=   Focal dystonia as the presenting sign in Creutzfeldt-Jakob disease
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Wicri

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