CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy
Identifieur interne :
003325 ( PascalFrancis/Curation );
précédent :
003324;
suivant :
003326
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. HardingSource :
-
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 :
English descriptors
pA |
A01 | 01 | 1 | | @0 0885-3185 |
---|
A03 | | 1 | | @0 Mov. disord. |
---|
A05 | | | | @2 10 |
---|
A06 | | | | @2 3 |
---|
A08 | 01 | 1 | ENG | @1 CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy |
---|
A11 | 01 | 1 | | @1 PLANTE-BORDENEUVE (V.) |
---|
A11 | 02 | 1 | | @1 BANDMANN (O.) |
---|
A11 | 03 | 1 | | @1 WENNING (G.) |
---|
A11 | 04 | 1 | | @1 QUINN (N. P.) |
---|
A11 | 05 | 1 | | @1 DANIEL (S. E.) |
---|
A11 | 06 | 1 | | @1 HARDING (A. E.) |
---|
A14 | 01 | | | @1 Inst. neurology, univ. dep. clin. neurology @2 London WC1N 3BG @3 GBR |
---|
A20 | | | | @1 277-278 |
---|
A21 | | | | @1 1995 |
---|
A23 | 01 | | | @0 ENG |
---|
A43 | 01 | | | @1 INIST @2 20953 @5 354000050919630060 |
---|
A44 | | | | @0 0000 |
---|
A45 | | | | @0 10 ref. |
---|
A47 | 01 | 1 | | @0 95-0363321 |
---|
A60 | | | | @1 P |
---|
A61 | | | | @0 A |
---|
A64 | 01 | 1 | | @0 Movement disorders |
---|
A66 | 01 | | | @0 USA |
---|
C02 | 01 | X | | @0 002B17G |
---|
C03 | 01 | X | FRE | @0 Parkinson maladie @5 01 |
---|
C03 | 01 | X | ENG | @0 Parkinson disease @5 01 |
---|
C03 | 01 | X | SPA | @0 Parkinson enfermedad @5 01 |
---|
C03 | 02 | X | FRE | @0 Polymorphisme @5 04 |
---|
C03 | 02 | X | ENG | @0 Polymorphism @5 04 |
---|
C03 | 02 | X | SPA | @0 Polimorfismo @5 04 |
---|
C03 | 03 | X | FRE | @0 Gène @5 05 |
---|
C03 | 03 | X | ENG | @0 Gene @5 05 |
---|
C03 | 03 | X | SPA | @0 Gen @5 05 |
---|
C03 | 04 | X | FRE | @0 Cytochrome P450 @5 07 |
---|
C03 | 04 | X | ENG | @0 Cytochrome P450 @5 07 |
---|
C03 | 04 | X | SPA | @0 Citocromo P450 @5 07 |
---|
C03 | 05 | X | FRE | @0 Débrisoquine @2 NK @2 FR @5 10 |
---|
C03 | 06 | X | FRE | @0 Hydroxylase @2 FE @5 13 |
---|
C03 | 06 | X | ENG | @0 Hydroxylase @2 FE @5 13 |
---|
C03 | 06 | X | SPA | @0 Hydroxylase @2 FE @5 13 |
---|
C03 | 07 | X | FRE | @0 Etude comparative @5 16 |
---|
C03 | 07 | X | ENG | @0 Comparative study @5 16 |
---|
C03 | 07 | X | GER | @0 Vergleich @5 16 |
---|
C03 | 07 | X | SPA | @0 Estudio comparativo @5 16 |
---|
C03 | 08 | X | FRE | @0 Exploration @5 17 |
---|
C03 | 08 | X | ENG | @0 Exploration @5 17 |
---|
C03 | 08 | X | SPA | @0 Exploración @5 17 |
---|
C03 | 09 | X | FRE | @0 Homme @5 20 |
---|
C03 | 09 | X | ENG | @0 Human @5 20 |
---|
C03 | 09 | X | SPA | @0 Hombre @5 20 |
---|
C03 | 10 | X | FRE | @0 CYP2D6 @4 INC @5 86 |
---|
C03 | 11 | X | FRE | @0 Atrophie multisystématisée @4 CD @5 96 |
---|
C03 | 11 | X | ENG | @0 Multiple system atrophy @4 CD @5 96 |
---|
C07 | 01 | X | FRE | @0 Enzyme |
---|
C07 | 01 | X | ENG | @0 Enzyme |
---|
C07 | 01 | X | SPA | @0 Enzima |
---|
C07 | 02 | X | FRE | @0 Système nerveux pathologie @5 37 |
---|
C07 | 02 | X | ENG | @0 Nervous system diseases @5 37 |
---|
C07 | 02 | X | SPA | @0 Sistema nervioso patología @5 37 |
---|
C07 | 03 | X | FRE | @0 Système nerveux central pathologie @5 38 |
---|
C07 | 03 | X | ENG | @0 Central nervous system disease @5 38 |
---|
C07 | 03 | X | SPA | @0 Sistema nervosio central patología @5 38 |
---|
C07 | 04 | X | FRE | @0 Encéphale pathologie @5 39 |
---|
C07 | 04 | X | ENG | @0 Cerebral disorder @5 39 |
---|
C07 | 04 | X | SPA | @0 Encéfalo patología @5 39 |
---|
C07 | 05 | X | FRE | @0 Extrapyramidal syndrome @5 40 |
---|
C07 | 05 | X | ENG | @0 Extrapyramidal syndrome @5 40 |
---|
C07 | 05 | X | SPA | @0 Extrapiramidal síndrome @5 40 |
---|
C07 | 06 | X | FRE | @0 Maladie dégénérative @5 41 |
---|
C07 | 06 | X | ENG | @0 Degenerative disease @5 41 |
---|
C07 | 06 | X | SPA | @0 Enfermedad degenerativa @5 41 |
---|
N21 | | | | @1 205 |
---|
|
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: Pour aller vers cette notice dans l'étape Curation :003499
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>
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<country>Royaume-Uni</country>
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<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>
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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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<term>Hydroxylase</term>
<term>Etude comparative</term>
<term>Exploration</term>
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<term>CYP2D6</term>
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<s5>01</s5>
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<s5>01</s5>
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<fC03 i1="02" i2="X" l="FRE"><s0>Polymorphisme</s0>
<s5>04</s5>
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<s5>04</s5>
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<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Gène</s0>
<s5>05</s5>
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<s5>07</s5>
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<s5>07</s5>
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<fC03 i1="05" i2="X" l="FRE"><s0>Débrisoquine</s0>
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<s2>FR</s2>
<s5>10</s5>
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<fC03 i1="06" i2="X" l="FRE"><s0>Hydroxylase</s0>
<s2>FE</s2>
<s5>13</s5>
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<s2>FE</s2>
<s5>13</s5>
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<fC03 i1="06" i2="X" l="SPA"><s0>Hydroxylase</s0>
<s2>FE</s2>
<s5>13</s5>
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<s5>16</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Comparative study</s0>
<s5>16</s5>
</fC03>
<fC03 i1="07" i2="X" l="GER"><s0>Vergleich</s0>
<s5>16</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Estudio comparativo</s0>
<s5>16</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Exploration</s0>
<s5>17</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Exploration</s0>
<s5>17</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Exploración</s0>
<s5>17</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Homme</s0>
<s5>20</s5>
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<fC03 i1="09" i2="X" l="ENG"><s0>Human</s0>
<s5>20</s5>
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<fC03 i1="09" i2="X" l="SPA"><s0>Hombre</s0>
<s5>20</s5>
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<s4>INC</s4>
<s5>86</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Atrophie multisystématisée</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Multiple system atrophy</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Enzyme</s0>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Enzyme</s0>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Enzima</s0>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>38</s5>
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<fC07 i1="03" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>38</s5>
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<fC07 i1="03" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07>
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<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fN21><s1>205</s1>
</fN21>
</pA>
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</inist>
</record>
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