MovDisordV3, Main, Merge, bibRecord, 008C12

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Identifieur interne : 008C12 ( Main/Merge ); précédent : 008C11; suivant : 008C13

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Auteurs : V. Plante-Bordeneuve [Royaume-Uni] ; O. Bandmann ; G. Wenning ; N. P. Quinn ; S. E. Daniel ; A. E. Harding

Source :

Movement disorders [ 0885-3185 ] ; 1995.

RBID : Pascal:95-0363321

Descripteurs français

Pascal (Inist)
- Parkinson maladie, Polymorphisme, Gène, Cytochrome P450, Débrisoquine, Hydroxylase, Etude comparative, Exploration, Homme, CYP2D6, Atrophie multisystématisée.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Comparative study, Cytochrome P450, Exploration, Gene, Human, Hydroxylase, Multiple system atrophy, Parkinson disease, Polymorphism.

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

to stream PascalFrancis, to step Corpus: 003499
to stream PascalFrancis, to step Curation: 003325
to stream PascalFrancis, to step Checkpoint: 003515

Links to Exploration step

Pascal:95-0363321

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy</title>
<author><name sortKey="Plante Bordeneuve, V" sort="Plante Bordeneuve, V" uniqKey="Plante Bordeneuve V" first="V." last="Plante-Bordeneuve">V. Plante-Bordeneuve</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Inst. neurology, univ. dep. clin. neurology</s1>
<s2>London WC1N 3BG</s2>
<s3>GBR</s3>
</inist:fA14>
<country>Royaume-Uni</country>
<wicri:noRegion>London WC1N 3BG</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Bandmann, O" sort="Bandmann, O" uniqKey="Bandmann O" first="O." last="Bandmann">O. Bandmann</name>
</author>
<author><name sortKey="Wenning, G" sort="Wenning, G" uniqKey="Wenning G" first="G." last="Wenning">G. Wenning</name>
</author>
<author><name sortKey="Quinn, N P" sort="Quinn, N P" uniqKey="Quinn N" first="N. P." last="Quinn">N. P. Quinn</name>
</author>
<author><name sortKey="Daniel, S E" sort="Daniel, S E" uniqKey="Daniel S" first="S. E." last="Daniel">S. E. Daniel</name>
</author>
<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">95-0363321</idno>
<date when="1995">1995</date>
<idno type="stanalyst">PASCAL 95-0363321 INIST</idno>
<idno type="RBID">Pascal:95-0363321</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003499</idno>
<idno type="wicri:Area/PascalFrancis/Curation">003325</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">003515</idno>
<idno type="wicri:doubleKey">0885-3185:1995:Plante Bordeneuve V:cyp:d:debrisoquine</idno>
<idno type="wicri:Area/Main/Merge">008C12</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy</title>
<author><name sortKey="Plante Bordeneuve, V" sort="Plante Bordeneuve, V" uniqKey="Plante Bordeneuve V" first="V." last="Plante-Bordeneuve">V. Plante-Bordeneuve</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Inst. neurology, univ. dep. clin. neurology</s1>
<s2>London WC1N 3BG</s2>
<s3>GBR</s3>
</inist:fA14>
<country>Royaume-Uni</country>
<wicri:noRegion>London WC1N 3BG</wicri:noRegion>
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</author>
<author><name sortKey="Bandmann, O" sort="Bandmann, O" uniqKey="Bandmann O" first="O." last="Bandmann">O. Bandmann</name>
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<author><name sortKey="Wenning, G" sort="Wenning, G" uniqKey="Wenning G" first="G." last="Wenning">G. Wenning</name>
</author>
<author><name sortKey="Quinn, N P" sort="Quinn, N P" uniqKey="Quinn N" first="N. P." last="Quinn">N. P. Quinn</name>
</author>
<author><name sortKey="Daniel, S E" sort="Daniel, S E" uniqKey="Daniel S" first="S. E." last="Daniel">S. E. Daniel</name>
</author>
<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="1995">1995</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
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</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Comparative study</term>
<term>Cytochrome P450</term>
<term>Exploration</term>
<term>Gene</term>
<term>Human</term>
<term>Hydroxylase</term>
<term>Multiple system atrophy</term>
<term>Parkinson disease</term>
<term>Polymorphism</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Parkinson maladie</term>
<term>Polymorphisme</term>
<term>Gène</term>
<term>Cytochrome P450</term>
<term>Débrisoquine</term>
<term>Hydroxylase</term>
<term>Etude comparative</term>
<term>Exploration</term>
<term>Homme</term>
<term>CYP2D6</term>
<term>Atrophie multisystématisée</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list><country><li>Royaume-Uni</li>
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<tree><noCountry><name sortKey="Bandmann, O" sort="Bandmann, O" uniqKey="Bandmann O" first="O." last="Bandmann">O. Bandmann</name>
<name sortKey="Daniel, S E" sort="Daniel, S E" uniqKey="Daniel S" first="S. E." last="Daniel">S. E. Daniel</name>
<name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
<name sortKey="Quinn, N P" sort="Quinn, N P" uniqKey="Quinn N" first="N. P." last="Quinn">N. P. Quinn</name>
<name sortKey="Wenning, G" sort="Wenning, G" uniqKey="Wenning G" first="G." last="Wenning">G. Wenning</name>
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<country name="Royaume-Uni"><noRegion><name sortKey="Plante Bordeneuve, V" sort="Plante Bordeneuve, V" uniqKey="Plante Bordeneuve V" first="V." last="Plante-Bordeneuve">V. Plante-Bordeneuve</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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	Movement Disorders (revue)
	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.

Movement Disorders (revue)

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Source :

Descripteurs français

English descriptors

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

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri