Movement Disorders (revue)

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MR-Spectroscopic Findings in Juvenile-Onset Huntington's Disease

Identifieur interne : 001C29 ( PascalFrancis/Curation ); précédent : 001C28; suivant : 001C30

MR-Spectroscopic Findings in Juvenile-Onset Huntington's Disease

Auteurs : Norman C. Reynolds [États-Unis] ; Robert W. Prost [États-Unis] ; Leighton P. Mark [États-Unis] ; Suja A. Joseph [États-Unis]

Source :

RBID : Pascal:08-0522191

Descripteurs français

English descriptors

Abstract

Seven HD gene positive individuals under the age of 21 years are described with clinical examination and proton-MR-spectroscopy (1H-MRS) profiles of the putamen. Despite clinical variability, the predominate 1H-MRS abnormality is elevated glutamate, expressed well beyond the confines of the basal ganglia, and low striatal creatine.
pA  
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A03   1    @0 Mov. disord.
A05       @2 23
A06       @2 13
A08 01  1  ENG  @1 MR-Spectroscopic Findings in Juvenile-Onset Huntington's Disease
A11 01  1    @1 REYNOLDS (Norman C.)
A11 02  1    @1 PROST (Robert W.)
A11 03  1    @1 MARK (Leighton P.)
A11 04  1    @1 JOSEPH (Suja A.)
A14 01      @1 Department of Neurology, VA Medical Center @2 Milwaukee, Wisconsin @3 USA @Z 1 aut.
A14 02      @1 Department of Radiology, Medical College of Wisconsin @2 Milwaukee, Wisconsin @3 USA @Z 2 aut. @Z 3 aut.
A14 03      @1 Department of Neurology, Medical College of Wisconsin @2 Milwaukee, Wisconsin @3 USA @Z 4 aut.
A20       @1 1931-1935
A21       @1 2008
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A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
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A60       @1 P @3 CC
A61       @0 A
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C01 01    ENG  @0 Seven HD gene positive individuals under the age of 21 years are described with clinical examination and proton-MR-spectroscopy (1H-MRS) profiles of the putamen. Despite clinical variability, the predominate 1H-MRS abnormality is elevated glutamate, expressed well beyond the confines of the basal ganglia, and low striatal creatine.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Chorée de Huntington @5 01
C03 01  X  ENG  @0 Huntington disease @5 01
C03 01  X  SPA  @0 Corea Huntington @5 01
C03 02  X  FRE  @0 Pathologie du système nerveux @5 02
C03 02  X  ENG  @0 Nervous system diseases @5 02
C03 02  X  SPA  @0 Sistema nervioso patología @5 02
C07 01  X  FRE  @0 Pathologie de l'encéphale @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Syndrome extrapyramidal @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Maladie héréditaire @5 40
C07 04  X  ENG  @0 Genetic disease @5 40
C07 04  X  SPA  @0 Enfermedad hereditaria @5 40
C07 05  X  FRE  @0 Pathologie du système nerveux central @5 41
C07 05  X  ENG  @0 Central nervous system disease @5 41
C07 05  X  SPA  @0 Sistema nervosio central patología @5 41
N21       @1 343
N44 01      @1 OTO
N82       @1 OTO

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Pascal:08-0522191

Le document en format XML

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