Parkinson's disease : A broken nosology
Identifieur interne : 001D81 ( PascalFrancis/Corpus ); précédent : 001D80; suivant : 001D82Parkinson's disease : A broken nosology
Auteurs : John Hardy ; Andrew J. LeesSource :
- Movement disorders [ 0885-3185 ] ; 2005.
Descripteurs français
- Pascal (Inist)
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.
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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:05-0457450Le document en format XML
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<server><NO>PASCAL 05-0457450 INIST</NO>
<ET>Parkinson's disease : A broken nosology</ET>
<AU>HARDY (John); LEES (Andrew J.); POEWE (Werner); WENNING (Gregor K.)</AU>
<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.)</AF>
<DT>Publication en série; Congrès; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. SUP12; S2-S4; Bibl. 34 ref.</SO>
<LA>Anglais</LA>
<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.</EA>
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