La maladie de Parkinson en France (serveur d'exploration)

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Are explicit memory disorders of progressive supranuclear palsy related to damage to striatofrontal circuits ? : Comparison with Alzheimer's, Parkinson's, and Huntington's diseases

Identifieur interne : 001699 ( PascalFrancis/Curation ); précédent : 001698; suivant : 001700

Are explicit memory disorders of progressive supranuclear palsy related to damage to striatofrontal circuits ? : Comparison with Alzheimer's, Parkinson's, and Huntington's diseases

Auteurs : B. Pillon [France] ; B. Deweer ; A. Michon ; C. Malapani ; Y. Agid ; B. Dubois

Source :

RBID : Pascal:94-0580570

Descripteurs français

English descriptors

Abstract

To test the hypothesis that memory disorders of subcortico-frontal dementia result mainly from inefficiency of retrieval processes of stored information, we compared verbal learning in 15 patients with progressive supranuclear palsy, prototypical of «subcortical dementia,» in free (California Verbal Learning Test) and controlled (Grober and Buschke's Test) encoding situations, with that of 19 controls, matched for age and level of education. The progressive supranuclear palsy patients showed memory deficits characterized by impaired immediate memory span, disturbed learning and consistency of recall, and abnormal number of false alarms at recognition, which were dramatically alleviated by controlled encoding associated with cued recall, using the same semantic cues
pA  
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A03   1    @0 Neurology
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A08 01  1  ENG  @1 Are explicit memory disorders of progressive supranuclear palsy related to damage to striatofrontal circuits ? : Comparison with Alzheimer's, Parkinson's, and Huntington's diseases
A11 01  1    @1 PILLON (B.)
A11 02  1    @1 DEWEER (B.)
A11 03  1    @1 MICHON (A.)
A11 04  1    @1 MALAPANI (C.)
A11 05  1    @1 AGID (Y.)
A11 06  1    @1 DUBOIS (B.)
A14 01      @1 INSERM, U 289 serv. neurologie neuropsychiatrie @2 75651 Paris @3 FRA
A20       @1 1264-1270
A21       @1 1994
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C01 01    ENG  @0 To test the hypothesis that memory disorders of subcortico-frontal dementia result mainly from inefficiency of retrieval processes of stored information, we compared verbal learning in 15 patients with progressive supranuclear palsy, prototypical of «subcortical dementia,» in free (California Verbal Learning Test) and controlled (Grober and Buschke's Test) encoding situations, with that of 19 controls, matched for age and level of education. The progressive supranuclear palsy patients showed memory deficits characterized by impaired immediate memory span, disturbed learning and consistency of recall, and abnormal number of false alarms at recognition, which were dramatically alleviated by controlled encoding associated with cued recall, using the same semantic cues
C02 01  X    @0 002B17G
C03 01  X  FRE  @0 Ophtalmoplégie supranucléaire @2 NM @5 01
C03 01  X  ENG  @0 Supranuclear ophthalmoplegia @2 NM @5 01
C03 01  X  SPA  @0 Oftalmoplejía supranuclear @2 NM @5 01
C03 02  X  FRE  @0 Trouble mémoire @5 04
C03 02  X  ENG  @0 Memory disorder @5 04
C03 02  X  SPA  @0 Trastorno memoria @5 04
C03 03  X  FRE  @0 Démence Alzheimer @2 NM @5 07
C03 03  X  ENG  @0 Alzheimer disease @2 NM @5 07
C03 03  X  SPA  @0 Demencia Alzheimer @2 NM @5 07
C03 04  X  FRE  @0 Chorée Huntington @2 NM @5 10
C03 04  X  ENG  @0 Huntington disease @2 NM @5 10
C03 04  X  SPA  @0 Corea Huntington @2 NM @5 10
C03 05  X  FRE  @0 Voie nigrostriatale @5 16
C03 05  X  ENG  @0 Nigrostriatal pathway @5 16
C03 05  X  SPA  @0 Vía nigroestriatal @5 16
C03 06  X  FRE  @0 Pathogénie @5 17
C03 06  X  ENG  @0 Pathogenesis @5 17
C03 06  X  SPA  @0 Patogenia @5 17
C03 07  X  FRE  @0 Homme @5 20
C03 07  X  ENG  @0 Human @5 20
C03 07  X  SPA  @0 Hombre @5 20
C07 01  X  FRE  @0 Oeil pathologie @5 37
C07 01  X  ENG  @0 Eye disease @5 37
C07 01  X  SPA  @0 Ojo patología @5 37
C07 02  X  FRE  @0 Oculomotricité syndrome @5 38
C07 02  X  ENG  @0 Oculomotor syndrome @5 38
C07 02  X  SPA  @0 Oculomotricidad síndrome @5 38
C07 03  X  FRE  @0 Système nerveux pathologie @5 39
C07 03  X  ENG  @0 Nervous system diseases @5 39
C07 03  X  SPA  @0 Sistema nervioso patología @5 39
C07 04  X  FRE  @0 Système nerveux central pathologie @5 40
C07 04  X  ENG  @0 Central nervous system disease @5 40
C07 04  X  SPA  @0 Sistema nervosio central patología @5 40
C07 05  X  FRE  @0 Tronc cérébral syndrome @5 41
C07 05  X  ENG  @0 Brain stem syndrome @5 41
C07 05  X  SPA  @0 Tallo encefalico sindrome @5 41
C07 06  X  FRE  @0 Encéphale pathologie @5 42
C07 06  X  ENG  @0 Cerebral disorder @5 42
C07 06  X  SPA  @0 Encéfalo patología @5 42
C07 07  X  FRE  @0 Maladie dégénérative @5 43
C07 07  X  ENG  @0 Degenerative disease @5 43
C07 07  X  SPA  @0 Enfermedad degenerativa @5 43
C07 08  X  FRE  @0 Trouble cognition @5 45
C07 08  X  ENG  @0 Cognitive disorder @5 45
C07 08  X  SPA  @0 Trastorno cognitivo @5 45
C07 09  X  FRE  @0 Extrapyramidal syndrome @5 64
C07 09  X  ENG  @0 Extrapyramidal syndrome @5 64
C07 09  X  SPA  @0 Extrapiramidal síndrome @5 64
C07 10  X  FRE  @0 Maladie héréditaire @5 66
C07 10  X  ENG  @0 Genetic disease @5 66
C07 10  X  SPA  @0 Enfermedad hereditaria @5 66
N21       @1 283

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Pascal:94-0580570

Le document en format XML

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