Lack of relation between genetic polymorphism of cytochrome p-450IID6 and sporadic idiopathic Parkinson's disease
Identifieur interne :
001804 ( PascalFrancis/Corpus );
précédent :
001803;
suivant :
001805
Lack of relation between genetic polymorphism of cytochrome p-450IID6 and sporadic idiopathic Parkinson's disease
Auteurs : R. Bordet ;
F. Broly ;
A. Destee ;
C. Libersa ;
J. LafitteSource :
-
Clinical neuropharmacology [ 0362-5664 ] ; 1996.
RBID : Pascal:96-0305267
Descripteurs français
English descriptors
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
A01 | 01 | 1 | | @0 0362-5664 |
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A02 | 01 | | | @0 CLNEDB |
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A03 | | 1 | | @0 Clin. neuropharmacol. |
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A05 | | | | @2 19 |
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A06 | | | | @2 3 |
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A08 | 01 | 1 | ENG | @1 Lack of relation between genetic polymorphism of cytochrome p-450IID6 and sporadic idiopathic Parkinson's disease |
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A11 | 01 | 1 | | @1 BORDET (R.) |
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A11 | 02 | 1 | | @1 BROLY (F.) |
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A11 | 03 | 1 | | @1 DESTEE (A.) |
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A11 | 04 | 1 | | @1 LIBERSA (C.) |
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A11 | 05 | 1 | | @1 LAFITTE (J.) |
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A14 | 01 | | | @1 Service de Neurologie A, CH et U de Lille @2 Lille @3 FRA @Z 1 aut. @Z 3 aut. |
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A14 | 02 | | | @1 Service de Biochimie et de Biologie Moléculaire, CH et U de Lille @2 Lille @3 FRA @Z 2 aut. |
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A14 | 03 | | | @1 Service de Pharmacologie Hospitalière, CH et U de Lille @2 Lille @3 FRA @Z 1 aut. @Z 4 aut. |
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A14 | 04 | | | @1 Service de Pneumologie, CH et U de Lille @2 Lille @3 FRA @Z 5 aut. |
---|
A20 | | | | @1 213-221 |
---|
A21 | | | | @1 1996 |
---|
A23 | 01 | | | @0 ENG |
---|
A43 | 01 | | | @1 INIST @2 16720 @5 354000043704830025 |
---|
A44 | | | | @0 0000 @1 © 1996 INIST-CNRS. All rights reserved. |
---|
A45 | | | | @0 46 ref. |
---|
A47 | 01 | 1 | | @0 96-0305267 |
---|
A60 | | | | @1 P |
---|
A61 | | | | @0 A |
---|
A64 | 01 | 1 | | @0 Clinical neuropharmacology |
---|
A66 | 01 | | | @0 USA |
---|
C02 | 01 | X | | @0 002B17G |
---|
C03 | 01 | X | FRE | @0 Homme @5 01 |
---|
C03 | 01 | X | ENG | @0 Human @5 01 |
---|
C03 | 01 | X | SPA | @0 Hombre @5 01 |
---|
C03 | 02 | X | FRE | @0 Génétique @5 04 |
---|
C03 | 02 | X | ENG | @0 Genetics @5 04 |
---|
C03 | 02 | X | SPA | @0 Genética @5 04 |
---|
C03 | 03 | X | FRE | @0 Polymorphisme @5 07 |
---|
C03 | 03 | X | ENG | @0 Polymorphism @5 07 |
---|
C03 | 03 | X | SPA | @0 Polimorfismo @5 07 |
---|
C03 | 04 | X | FRE | @0 Parkinson maladie @5 10 |
---|
C03 | 04 | X | ENG | @0 Parkinson disease @5 10 |
---|
C03 | 04 | X | SPA | @0 Parkinson enfermedad @5 10 |
---|
C03 | 05 | X | FRE | @0 Cytochrome P450 @5 13 |
---|
C03 | 05 | X | ENG | @0 Cytochrome P450 @5 13 |
---|
C03 | 05 | X | SPA | @0 Citocromo P450 @5 13 |
---|
C03 | 06 | X | FRE | @0 Isozyme @5 14 |
---|
C03 | 06 | X | ENG | @0 Isozyme @5 14 |
---|
C03 | 06 | X | SPA | @0 Isozima @5 14 |
---|
C03 | 07 | X | FRE | @0 Phénotype hydroxylateur @5 16 |
---|
C03 | 07 | X | ENG | @0 Hydroxylator phenotype @5 16 |
---|
C03 | 07 | X | SPA | @0 Fenotipo hidroxilador @5 16 |
---|
C03 | 08 | X | FRE | @0 Déterminisme génétique @5 17 |
---|
C03 | 08 | X | ENG | @0 Genetic inheritance @5 17 |
---|
C03 | 08 | X | SPA | @0 Determinismo genético @5 17 |
---|
C03 | 09 | X | FRE | @0 Etiologie @5 18 |
---|
C03 | 09 | X | ENG | @0 Etiology @5 18 |
---|
C03 | 09 | X | SPA | @0 Etiología @5 18 |
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C03 | 10 | X | FRE | @0 Gène CYP2D6 @4 INC @5 86 |
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C07 | 01 | X | FRE | @0 Système nerveux pathologie @5 61 |
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C07 | 01 | X | ENG | @0 Nervous system diseases @5 61 |
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C07 | 01 | X | SPA | @0 Sistema nervioso patología @5 61 |
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C07 | 02 | X | FRE | @0 Système nerveux central pathologie @5 62 |
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C07 | 02 | X | ENG | @0 Central nervous system disease @5 62 |
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C07 | 02 | X | SPA | @0 Sistema nervosio central patología @5 62 |
---|
C07 | 03 | X | FRE | @0 Encéphale pathologie @5 63 |
---|
C07 | 03 | X | ENG | @0 Cerebral disorder @5 63 |
---|
C07 | 03 | X | SPA | @0 Encéfalo patología @5 63 |
---|
C07 | 04 | X | FRE | @0 Extrapyramidal syndrome @5 64 |
---|
C07 | 04 | X | ENG | @0 Extrapyramidal syndrome @5 64 |
---|
C07 | 04 | X | SPA | @0 Extrapiramidal síndrome @5 64 |
---|
C07 | 05 | X | FRE | @0 Maladie dégénérative @5 65 |
---|
C07 | 05 | X | ENG | @0 Degenerative disease @5 65 |
---|
C07 | 05 | X | SPA | @0 Enfermedad degenerativa @5 65 |
---|
N21 | | | | @1 211 |
---|
|
Format Inist (serveur)
NO : | PASCAL 96-0305267 INIST |
ET : | Lack of relation between genetic polymorphism of cytochrome p-450IID6 and sporadic idiopathic Parkinson's disease |
AU : | BORDET (R.); BROLY (F.); DESTEE (A.); LIBERSA (C.); LAFITTE (J.) |
AF : | Service de Neurologie A, CH et U de Lille/Lille/France (1 aut., 3 aut.); Service de Biochimie et de Biologie Moléculaire, CH et U de Lille/Lille/France (2 aut.); Service de Pharmacologie Hospitalière, CH et U de Lille/Lille/France (1 aut., 4 aut.); Service de Pneumologie, CH et U de Lille/Lille/France (5 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Clinical neuropharmacology; ISSN 0362-5664; Coden CLNEDB; Etats-Unis; Da. 1996; Vol. 19; No. 3; Pp. 213-221; Bibl. 46 ref. |
LA : | Anglais |
CC : | 002B17G |
FD : | Homme; Génétique; Polymorphisme; Parkinson maladie; Cytochrome P450; Isozyme; Phénotype hydroxylateur; Déterminisme génétique; Etiologie; Gène CYP2D6 |
FG : | Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative |
ED : | Human; Genetics; Polymorphism; Parkinson disease; Cytochrome P450; Isozyme; Hydroxylator phenotype; Genetic inheritance; Etiology |
EG : | Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease |
SD : | Hombre; Genética; Polimorfismo; Parkinson enfermedad; Citocromo P450; Isozima; Fenotipo hidroxilador; Determinismo genético; Etiología |
LO : | INIST-16720.354000043704830025 |
ID : | 96-0305267 |
Links to Exploration step
Pascal:96-0305267
Le document en format XML
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<server><NO>PASCAL 96-0305267 INIST</NO>
<ET>Lack of relation between genetic polymorphism of cytochrome p-450IID6 and sporadic idiopathic Parkinson's disease</ET>
<AU>BORDET (R.); BROLY (F.); DESTEE (A.); LIBERSA (C.); LAFITTE (J.)</AU>
<AF>Service de Neurologie A, CH et U de Lille/Lille/France (1 aut., 3 aut.); Service de Biochimie et de Biologie Moléculaire, CH et U de Lille/Lille/France (2 aut.); Service de Pharmacologie Hospitalière, CH et U de Lille/Lille/France (1 aut., 4 aut.); Service de Pneumologie, CH et U de Lille/Lille/France (5 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Clinical neuropharmacology; ISSN 0362-5664; Coden CLNEDB; Etats-Unis; Da. 1996; Vol. 19; No. 3; Pp. 213-221; Bibl. 46 ref.</SO>
<LA>Anglais</LA>
<CC>002B17G</CC>
<FD>Homme; Génétique; Polymorphisme; Parkinson maladie; Cytochrome P450; Isozyme; Phénotype hydroxylateur; Déterminisme génétique; Etiologie; Gène CYP2D6</FD>
<FG>Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative</FG>
<ED>Human; Genetics; Polymorphism; Parkinson disease; Cytochrome P450; Isozyme; Hydroxylator phenotype; Genetic inheritance; Etiology</ED>
<EG>Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease</EG>
<SD>Hombre; Genética; Polimorfismo; Parkinson enfermedad; Citocromo P450; Isozima; Fenotipo hidroxilador; Determinismo genético; Etiología</SD>
<LO>INIST-16720.354000043704830025</LO>
<ID>96-0305267</ID>
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