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

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease

Identifieur interne : 000656 ( PascalFrancis/Curation ); précédent : 000655; suivant : 000657

Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease

Auteurs : Vincent Paille [France] ; Philippe Brachet [France] ; Philippe Damier [France]

Source :

RBID : Pascal:04-0446932

Descripteurs français

English descriptors

Abstract

The pathogenesis of the motor fluctuations and dyskinesias that complicate levodopa treatment for Parkinson's disease (PD) remains uncertain. To evaluate the relationship between the degree of dopamine neuron loss and the severity of dyskinesias in a rodent model of PD, Sprague-Dawley rats were lesioned unilaterally using different doses of 6-hydroxydopamine injected into the substantia nigra pars compacta (SNc). All rats received two daily oral doses of levodopa for one month. In most of the animals chronic levodopa administration induced abnormal involuntary movements (AIMs), which were in some respects similar to human dyskinesias.We found that a minimum dopamine cell loss of around 95% was required for the development of dyskinesias after one-month of levodopa treatment. Moreover, we observed a positive relationship between the percentage dopaminergic cell loss in the SNc and the severity of levodopa-induced AIMs.
pA  
A01 01  1    @0 0959-4965
A03   1    @0 Neuroreport : (Oxf.)
A05       @2 15
A06       @2 3
A08 01  1  ENG  @1 Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease
A11 01  1    @1 PAILLE (Vincent)
A11 02  1    @1 BRACHET (Philippe)
A11 03  1    @1 DAMIER (Philippe)
A14 01      @1 INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet @2 44093 Nantes @3 FRA @Z 1 aut. @Z 2 aut. @Z 3 aut.
A14 02      @1 Clinique Neurologique and Centre d'Investigation Clinique, CHU @2 Nantes @3 FRA @Z 3 aut.
A20       @1 561-564
A21       @1 2004
A23 01      @0 ENG
A43 01      @1 INIST @2 22534 @5 354000113564420350
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
A45       @0 21 ref.
A47 01  1    @0 04-0446932
A60       @1 P
A61       @0 A
A64 01  1    @0 Neuroreport : (Oxford)
A66 01      @0 GBR
C01 01    ENG  @0 The pathogenesis of the motor fluctuations and dyskinesias that complicate levodopa treatment for Parkinson's disease (PD) remains uncertain. To evaluate the relationship between the degree of dopamine neuron loss and the severity of dyskinesias in a rodent model of PD, Sprague-Dawley rats were lesioned unilaterally using different doses of 6-hydroxydopamine injected into the substantia nigra pars compacta (SNc). All rats received two daily oral doses of levodopa for one month. In most of the animals chronic levodopa administration induced abnormal involuntary movements (AIMs), which were in some respects similar to human dyskinesias.We found that a minimum dopamine cell loss of around 95% was required for the development of dyskinesias after one-month of levodopa treatment. Moreover, we observed a positive relationship between the percentage dopaminergic cell loss in the SNc and the severity of levodopa-induced AIMs.
C02 01  X    @0 002A25E
C02 02  X    @0 002B17A01
C03 01  X  FRE  @0 Lésion @5 01
C03 01  X  ENG  @0 Lesion @5 01
C03 01  X  SPA  @0 Lesión @5 01
C03 02  X  FRE  @0 Modèle animal @5 02
C03 02  X  ENG  @0 Animal model @5 02
C03 02  X  SPA  @0 Modelo animal @5 02
C03 03  X  FRE  @0 Pathogénie @5 03
C03 03  X  ENG  @0 Pathogenesis @5 03
C03 03  X  SPA  @0 Patogenia @5 03
C03 04  X  FRE  @0 Lévodopa @2 NK @2 FR @5 04
C03 04  X  ENG  @0 Levodopa @2 NK @2 FR @5 04
C03 04  X  SPA  @0 Levodopa @2 NK @2 FR @5 04
C03 05  X  FRE  @0 Neurone dopaminergique @5 05
C03 05  X  ENG  @0 Dopaminergic neuron @5 05
C03 05  X  SPA  @0 Neurona dopaminérgica @5 05
C03 06  X  FRE  @0 Mort cellulaire @5 06
C03 06  X  ENG  @0 Cell death @5 06
C03 06  X  SPA  @0 Muerte celular @5 06
C03 07  X  FRE  @0 Oxidopamine @2 NK @2 FR @5 07
C03 07  X  ENG  @0 Oxidopamine @2 NK @2 FR @5 07
C03 07  X  SPA  @0 Oxidopamina @2 NK @2 FR @5 07
C03 08  X  FRE  @0 Locus niger @5 08
C03 08  X  ENG  @0 Locus niger @5 08
C03 08  X  SPA  @0 Locus níger @5 08
C03 09  X  FRE  @0 Dyskinésie @5 09
C03 09  X  ENG  @0 Dyskinesia @5 09
C03 09  X  SPA  @0 Disquinesia @5 09
C03 10  X  FRE  @0 Chronique @5 10
C03 10  X  ENG  @0 Chronic @5 10
C03 10  X  SPA  @0 Crónico @5 10
C03 11  X  FRE  @0 Mouvement involontaire @5 11
C03 11  X  ENG  @0 Involuntary movement @5 11
C03 11  X  SPA  @0 Movimiento involuntario @5 11
C03 12  X  FRE  @0 Parkinson maladie @5 12
C03 12  X  ENG  @0 Parkinson disease @5 12
C03 12  X  SPA  @0 Parkinson enfermedad @5 12
C03 13  X  FRE  @0 Dopamine @2 NK @2 FR @5 13
C03 13  X  ENG  @0 Dopamine @2 NK @2 FR @5 13
C03 13  X  SPA  @0 Dopamina @2 NK @2 FR @5 13
C03 14  X  FRE  @0 Développement @5 14
C03 14  X  ENG  @0 Development @5 14
C03 14  X  SPA  @0 Desarrollo @5 14
C03 15  X  FRE  @0 Rat @5 54
C03 15  X  ENG  @0 Rat @5 54
C03 15  X  SPA  @0 Rata @5 54
C03 16  X  FRE  @0 Homme @5 55
C03 16  X  ENG  @0 Human @5 55
C03 16  X  SPA  @0 Hombre @5 55
C03 17  X  FRE  @0 Animal @5 69
C03 17  X  ENG  @0 Animal @5 69
C03 17  X  SPA  @0 Animal @5 69
C03 18  X  FRE  @0 Contrôle moteur @5 70
C03 18  X  ENG  @0 Motor control @5 70
C03 18  X  SPA  @0 Control motor @5 70
C07 01  X  FRE  @0 Extrapyramidal syndrome @5 20
C07 01  X  ENG  @0 Extrapyramidal syndrome @5 20
C07 01  X  SPA  @0 Extrapiramidal síndrome @5 20
C07 02  X  FRE  @0 Système nerveux pathologie @5 21
C07 02  X  ENG  @0 Nervous system diseases @5 21
C07 02  X  SPA  @0 Sistema nervioso patología @5 21
C07 03  X  FRE  @0 Trouble neurologique @5 22
C07 03  X  ENG  @0 Neurological disorder @5 22
C07 03  X  SPA  @0 Trastorno neurológico @5 22
C07 04  X  FRE  @0 Encéphale pathologie @5 23
C07 04  X  ENG  @0 Cerebral disorder @5 23
C07 04  X  SPA  @0 Encéfalo patología @5 23
C07 05  X  FRE  @0 Maladie dégénérative @5 24
C07 05  X  ENG  @0 Degenerative disease @5 24
C07 05  X  SPA  @0 Enfermedad degenerativa @5 24
C07 06  X  FRE  @0 Système nerveux central pathologie @5 25
C07 06  X  ENG  @0 Central nervous system disease @5 25
C07 06  X  SPA  @0 Sistema nervosio central patología @5 25
C07 07  X  FRE  @0 Antiparkinsonien @5 26
C07 07  X  ENG  @0 Antiparkinson agent @5 26
C07 07  X  SPA  @0 Antiparkinsoniano @5 26
C07 08  X  FRE  @0 Système nerveux central @5 27
C07 08  X  ENG  @0 Central nervous system @5 27
C07 08  X  SPA  @0 Sistema nervioso central @5 27
C07 09  X  FRE  @0 Catécholamine @5 28
C07 09  X  ENG  @0 Catecholamine @5 28
C07 09  X  SPA  @0 Catecolamina @5 28
C07 10  X  FRE  @0 Neurotransmetteur @5 29
C07 10  X  ENG  @0 Neurotransmitter @5 29
C07 10  X  SPA  @0 Neurotransmisor @5 29
C07 11  X  FRE  @0 Rodentia @2 NS
C07 11  X  ENG  @0 Rodentia @2 NS
C07 11  X  SPA  @0 Rodentia @2 NS
C07 12  X  FRE  @0 Mammalia @2 NS
C07 12  X  ENG  @0 Mammalia @2 NS
C07 12  X  SPA  @0 Mammalia @2 NS
C07 13  X  FRE  @0 Vertebrata @2 NS
C07 13  X  ENG  @0 Vertebrata @2 NS
C07 13  X  SPA  @0 Vertebrata @2 NS
N21       @1 250
N44 01      @1 OTO
N82       @1 OTO

Links toward previous steps (curation, corpus...)


Links to Exploration step

Pascal:04-0446932

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease</title>
<author>
<name sortKey="Paille, Vincent" sort="Paille, Vincent" uniqKey="Paille V" first="Vincent" last="Paille">Vincent Paille</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
<author>
<name sortKey="Brachet, Philippe" sort="Brachet, Philippe" uniqKey="Brachet P" first="Philippe" last="Brachet">Philippe Brachet</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
<author>
<name sortKey="Damier, Philippe" sort="Damier, Philippe" uniqKey="Damier P" first="Philippe" last="Damier">Philippe Damier</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Clinique Neurologique and Centre d'Investigation Clinique, CHU</s1>
<s2>Nantes</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">04-0446932</idno>
<date when="2004">2004</date>
<idno type="stanalyst">PASCAL 04-0446932 INIST</idno>
<idno type="RBID">Pascal:04-0446932</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000D78</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000656</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease</title>
<author>
<name sortKey="Paille, Vincent" sort="Paille, Vincent" uniqKey="Paille V" first="Vincent" last="Paille">Vincent Paille</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
<author>
<name sortKey="Brachet, Philippe" sort="Brachet, Philippe" uniqKey="Brachet P" first="Philippe" last="Brachet">Philippe Brachet</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
<author>
<name sortKey="Damier, Philippe" sort="Damier, Philippe" uniqKey="Damier P" first="Philippe" last="Damier">Philippe Damier</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Clinique Neurologique and Centre d'Investigation Clinique, CHU</s1>
<s2>Nantes</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Neuroreport : (Oxford)</title>
<title level="j" type="abbreviated">Neuroreport : (Oxf.)</title>
<idno type="ISSN">0959-4965</idno>
<imprint>
<date when="2004">2004</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Neuroreport : (Oxford)</title>
<title level="j" type="abbreviated">Neuroreport : (Oxf.)</title>
<idno type="ISSN">0959-4965</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Animal</term>
<term>Animal model</term>
<term>Cell death</term>
<term>Chronic</term>
<term>Development</term>
<term>Dopamine</term>
<term>Dopaminergic neuron</term>
<term>Dyskinesia</term>
<term>Human</term>
<term>Involuntary movement</term>
<term>Lesion</term>
<term>Levodopa</term>
<term>Locus niger</term>
<term>Motor control</term>
<term>Oxidopamine</term>
<term>Parkinson disease</term>
<term>Pathogenesis</term>
<term>Rat</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Lésion</term>
<term>Modèle animal</term>
<term>Pathogénie</term>
<term>Lévodopa</term>
<term>Neurone dopaminergique</term>
<term>Mort cellulaire</term>
<term>Oxidopamine</term>
<term>Locus niger</term>
<term>Dyskinésie</term>
<term>Chronique</term>
<term>Mouvement involontaire</term>
<term>Parkinson maladie</term>
<term>Dopamine</term>
<term>Développement</term>
<term>Rat</term>
<term>Homme</term>
<term>Animal</term>
<term>Contrôle moteur</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">The pathogenesis of the motor fluctuations and dyskinesias that complicate levodopa treatment for Parkinson's disease (PD) remains uncertain. To evaluate the relationship between the degree of dopamine neuron loss and the severity of dyskinesias in a rodent model of PD, Sprague-Dawley rats were lesioned unilaterally using different doses of 6-hydroxydopamine injected into the substantia nigra pars compacta (SNc). All rats received two daily oral doses of levodopa for one month. In most of the animals chronic levodopa administration induced abnormal involuntary movements (AIMs), which were in some respects similar to human dyskinesias.We found that a minimum dopamine cell loss of around 95% was required for the development of dyskinesias after one-month of levodopa treatment. Moreover, we observed a positive relationship between the percentage dopaminergic cell loss in the SNc and the severity of levodopa-induced AIMs.</div>
</front>
</TEI>
<inist>
<standard h6="B">
<pA>
<fA01 i1="01" i2="1">
<s0>0959-4965</s0>
</fA01>
<fA03 i2="1">
<s0>Neuroreport : (Oxf.)</s0>
</fA03>
<fA05>
<s2>15</s2>
</fA05>
<fA06>
<s2>3</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>PAILLE (Vincent)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>BRACHET (Philippe)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>DAMIER (Philippe)</s1>
</fA11>
<fA14 i1="01">
<s1>INSERM, Unité 437, CHU de Nantes, 30 bd Jean Monnet</s1>
<s2>44093 Nantes</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Clinique Neurologique and Centre d'Investigation Clinique, CHU</s1>
<s2>Nantes</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA20>
<s1>561-564</s1>
</fA20>
<fA21>
<s1>2004</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>22534</s2>
<s5>354000113564420350</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2004 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>21 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>04-0446932</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Neuroreport : (Oxford)</s0>
</fA64>
<fA66 i1="01">
<s0>GBR</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>The pathogenesis of the motor fluctuations and dyskinesias that complicate levodopa treatment for Parkinson's disease (PD) remains uncertain. To evaluate the relationship between the degree of dopamine neuron loss and the severity of dyskinesias in a rodent model of PD, Sprague-Dawley rats were lesioned unilaterally using different doses of 6-hydroxydopamine injected into the substantia nigra pars compacta (SNc). All rats received two daily oral doses of levodopa for one month. In most of the animals chronic levodopa administration induced abnormal involuntary movements (AIMs), which were in some respects similar to human dyskinesias.We found that a minimum dopamine cell loss of around 95% was required for the development of dyskinesias after one-month of levodopa treatment. Moreover, we observed a positive relationship between the percentage dopaminergic cell loss in the SNc and the severity of levodopa-induced AIMs.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002A25E</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B17A01</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Lésion</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Lesion</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Lesión</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Modèle animal</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Animal model</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Modelo animal</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Pathogénie</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Pathogenesis</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Patogenia</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Lévodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Levodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Levodopa</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Neurone dopaminergique</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Dopaminergic neuron</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Neurona dopaminérgica</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Mort cellulaire</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Cell death</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Muerte celular</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Oxidopamine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Oxidopamine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Oxidopamina</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Locus niger</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Locus niger</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Locus níger</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Dyskinésie</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Dyskinesia</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Disquinesia</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Chronique</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Chronic</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Crónico</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Parkinson maladie</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Parkinson disease</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Parkinson enfermedad</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Dopamine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Dopamine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Dopamina</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>13</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Développement</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Development</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Desarrollo</s0>
<s5>14</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE">
<s0>Rat</s0>
<s5>54</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG">
<s0>Rat</s0>
<s5>54</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA">
<s0>Rata</s0>
<s5>54</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE">
<s0>Homme</s0>
<s5>55</s5>
</fC03>
<fC03 i1="16" i2="X" l="ENG">
<s0>Human</s0>
<s5>55</s5>
</fC03>
<fC03 i1="16" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>55</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE">
<s0>Animal</s0>
<s5>69</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG">
<s0>Animal</s0>
<s5>69</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA">
<s0>Animal</s0>
<s5>69</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE">
<s0>Contrôle moteur</s0>
<s5>70</s5>
</fC03>
<fC03 i1="18" i2="X" l="ENG">
<s0>Motor control</s0>
<s5>70</s5>
</fC03>
<fC03 i1="18" i2="X" l="SPA">
<s0>Control motor</s0>
<s5>70</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Extrapyramidal syndrome</s0>
<s5>20</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>20</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>20</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>21</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>21</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>21</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>22</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>22</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>22</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<s5>23</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>23</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>23</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>24</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>24</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>24</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>25</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>25</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>25</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Antiparkinsonien</s0>
<s5>26</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Antiparkinson agent</s0>
<s5>26</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Antiparkinsoniano</s0>
<s5>26</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Système nerveux central</s0>
<s5>27</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Central nervous system</s0>
<s5>27</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Sistema nervioso central</s0>
<s5>27</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Catécholamine</s0>
<s5>28</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Catecholamine</s0>
<s5>28</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Catecolamina</s0>
<s5>28</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE">
<s0>Neurotransmetteur</s0>
<s5>29</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG">
<s0>Neurotransmitter</s0>
<s5>29</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA">
<s0>Neurotransmisor</s0>
<s5>29</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE">
<s0>Rodentia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="11" i2="X" l="ENG">
<s0>Rodentia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="11" i2="X" l="SPA">
<s0>Rodentia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="12" i2="X" l="FRE">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="12" i2="X" l="ENG">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="12" i2="X" l="SPA">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="13" i2="X" l="FRE">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="13" i2="X" l="ENG">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="13" i2="X" l="SPA">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fN21>
<s1>250</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonFranceV1/Data/PascalFrancis/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000656 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Curation/biblio.hfd -nk 000656 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    ParkinsonFranceV1
   |flux=    PascalFrancis
   |étape=   Curation
   |type=    RBID
   |clé=     Pascal:04-0446932
   |texte=   Role of nigral lesion in the genesis of dyskinesias in a rat model of Parkinson's disease
}}

Wicri

This area was generated with Dilib version V0.6.29.
Data generation: Wed May 17 19:46:39 2017. Site generation: Mon Mar 4 15:48:15 2024