CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy
Identifieur interne : 005A26 ( Main/Exploration ); précédent : 005A25; suivant : 005A27CYP2D6-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. HardingSource :
- Movement disorders [ 0885-3185 ] ; 1995.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
Affiliations:
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
- to stream Main, to step Merge: 008C12
- to stream Main, to step Curation: 005A26
Le document en format XML
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<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>
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<country>Royaume-Uni</country>
<wicri:noRegion>London WC1N 3BG</wicri:noRegion>
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<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>
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<author><name sortKey="Quinn, N P" sort="Quinn, N P" uniqKey="Quinn N" first="N. P." last="Quinn">N. P. Quinn</name>
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<author><name sortKey="Daniel, S E" sort="Daniel, S E" uniqKey="Daniel S" first="S. E." last="Daniel">S. E. Daniel</name>
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<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
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<author><name sortKey="Daniel, S E" sort="Daniel, S E" uniqKey="Daniel S" first="S. E." last="Daniel">S. E. Daniel</name>
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<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
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<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
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<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>
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<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
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<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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