Movement Disorders (revue)

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Parkinson's disease : A broken nosology

Identifieur interne : 001D81 ( PascalFrancis/Corpus ); précédent : 001D80; suivant : 001D82

Parkinson's disease : A broken nosology

Auteurs : John Hardy ; Andrew J. Lees

Source :

RBID : Pascal:05-0457450

Descripteurs français

English descriptors

Abstract

Parkinson's disease (PD) is a clinical diagnosis. We argue here that if we are to make progress in understanding its underlying pathogenesis, there is a need to have a pathological definition of disease that includes the presence of Lewy bodies and nigral loss in the ventrolateral tier of the pars compacta of the substantia nigra. Using such a definition, there is only one certain and known cause: mutations in the α-synuclein gene. However, the phenotype of this one known cause is broader than PD and encompasses Lewy body dementia.

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 20
A06       @3 SUP12
A08 01  1  ENG  @1 Parkinson's disease : A broken nosology
A09 01  1  ENG  @1 Atypical Parkinsonian Disorders
A11 01  1    @1 HARDY (John)
A11 02  1    @1 LEES (Andrew J.)
A12 01  1    @1 POEWE (Werner) @9 ed.
A12 02  1    @1 WENNING (Gregor K.) @9 ed.
A14 01      @1 Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health @2 Bethesda, Maryland @3 USA @Z 1 aut.
A14 02      @1 Reta Lila Weston Institute of Neurological Studies, University College London @2 London @3 GBR @Z 1 aut. @Z 2 aut.
A15 01      @1 Department of Neurology, Medical University Innsbruck @2 Innsbruck @3 AUT @Z 1 aut. @Z 2 aut.
A20       @2 S2-S4
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000132714250010
A44       @0 0000 @1 © 2005 INIST-CNRS. All rights reserved.
A45       @0 34 ref.
A47 01  1    @0 05-0457450
A60       @1 P @2 C
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 Parkinson's disease (PD) is a clinical diagnosis. We argue here that if we are to make progress in understanding its underlying pathogenesis, there is a need to have a pathological definition of disease that includes the presence of Lewy bodies and nigral loss in the ventrolateral tier of the pars compacta of the substantia nigra. Using such a definition, there is only one certain and known cause: mutations in the α-synuclein gene. However, the phenotype of this one known cause is broader than PD and encompasses Lewy body dementia.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C02 03  X    @0 002B17A03
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Parkinson maladie @5 02
C03 02  X  ENG  @0 Parkinson disease @5 02
C03 02  X  SPA  @0 Parkinson enfermedad @5 02
C03 03  X  FRE  @0 Nosologie @5 09
C03 03  X  ENG  @0 Nosology @5 09
C03 03  X  SPA  @0 Nosología @5 09
C03 04  X  FRE  @0 Démence corps Lewy @2 NM @5 10
C03 04  X  ENG  @0 Lewy body dementia @2 NM @5 10
C03 04  X  SPA  @0 Demencia cuerpos Lewy @2 NM @5 10
C07 01  X  FRE  @0 Encéphale pathologie @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 Extrapyramidal syndrome @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 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
N21       @1 318
N44 01      @1 OTO
N82       @1 OTO
pR  
A30 01  1  ENG  @1 Atypical Parkinsonian Disorders - From Protein Dysfunction to Therapeutic Intervention. International Meeting @3 Innsbruck AUT @4 2003-02-19

Format Inist (serveur)

NO : PASCAL 05-0457450 INIST
ET : Parkinson's disease : A broken nosology
AU : HARDY (John); LEES (Andrew J.); POEWE (Werner); WENNING (Gregor K.)
AF : Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health/Bethesda, Maryland/Etats-Unis (1 aut.); Reta Lila Weston Institute of Neurological Studies, University College London/London/Royaume-Uni (1 aut., 2 aut.); Department of Neurology, Medical University Innsbruck/Innsbruck/Autriche (1 aut., 2 aut.)
DT : Publication en série; Congrès; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. SUP12; S2-S4; Bibl. 34 ref.
LA : Anglais
EA : Parkinson's disease (PD) is a clinical diagnosis. We argue here that if we are to make progress in understanding its underlying pathogenesis, there is a need to have a pathological definition of disease that includes the presence of Lewy bodies and nigral loss in the ventrolateral tier of the pars compacta of the substantia nigra. Using such a definition, there is only one certain and known cause: mutations in the α-synuclein gene. However, the phenotype of this one known cause is broader than PD and encompasses Lewy body dementia.
CC : 002B17; 002B17G; 002B17A03
FD : Système nerveux pathologie; Parkinson maladie; Nosologie; Démence corps Lewy
FG : Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie
ED : Nervous system diseases; Parkinson disease; Nosology; Lewy body dementia
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease
SD : Sistema nervioso patología; Parkinson enfermedad; Nosología; Demencia cuerpos Lewy
LO : INIST-20953.354000132714250010
ID : 05-0457450

Links to Exploration step

Pascal:05-0457450

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