Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease
Identifieur interne : 003612 ( PascalFrancis/Corpus ); précédent : 003611; suivant : 003613Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease
Auteurs : G. S. Hotamisligil ; A. S. Girmen ; J. S. Fink ; E. Tivol ; C. Shalish ; J. Trofatter ; J. Baenziger ; S. Diamond ; C. Markham ; J. Sullivan ; J. Growdon ; X. O. BreakefieldSource :
- Movement disorders [ 0885-3185 ] ; 1994.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
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Format Inist (serveur)
NO : | PASCAL 94-0459266 INIST |
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ET : | Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease |
AU : | HOTAMISLIGIL (G. S.); GIRMEN (A. S.); FINK (J. S.); TIVOL (E.); SHALISH (C.); TROFATTER (J.); BAENZIGER (J.); DIAMOND (S.); MARKHAM (C.); SULLIVAN (J.); GROWDON (J.); BREAKEFIELD (X. O.) |
AF : | Massachusetts gen. hosp., neurology serv., molecular neurogenetics unit/Charlestown MA 02129/Etats-Unis (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 11 aut., 12 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1994; Vol. 9; No. 3; Pp. 305-310; Bibl. 72 ref. |
LA : | Anglais |
CC : | 002B17G |
FD : | Parkinson maladie; Génétique; Haplotype; Chromosome X; Amine oxidase (flavin-containing); Mâle; Homme; Exploration; Facteur risque |
FG : | Oxidoreductases; Enzyme; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative |
ED : | Parkinson disease; Genetics; Haplotype; X-Chromosome; Amine oxidase (flavin-containing); Male; Human; Exploration; Risk factor |
EG : | Oxidoreductases; Enzyme; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease |
SD : | Parkinson enfermedad; Genética; Haplotipo; Cromosoma X; Amine oxidase (flavin-containing); Macho; Hombre; Exploración; Factor riesgo |
LO : | INIST-20953.354000045669810030 |
ID : | 94-0459266 |
Links to Exploration step
Pascal:94-0459266Le document en format XML
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<s5>19</s5>
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<fC03 i1="09" i2="X" l="SPA"><s0>Factor riesgo</s0>
<s5>19</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fN21><s1>208</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 94-0459266 INIST</NO>
<ET>Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease</ET>
<AU>HOTAMISLIGIL (G. S.); GIRMEN (A. S.); FINK (J. S.); TIVOL (E.); SHALISH (C.); TROFATTER (J.); BAENZIGER (J.); DIAMOND (S.); MARKHAM (C.); SULLIVAN (J.); GROWDON (J.); BREAKEFIELD (X. O.)</AU>
<AF>Massachusetts gen. hosp., neurology serv., molecular neurogenetics unit/Charlestown MA 02129/Etats-Unis (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 11 aut., 12 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1994; Vol. 9; No. 3; Pp. 305-310; Bibl. 72 ref.</SO>
<LA>Anglais</LA>
<CC>002B17G</CC>
<FD>Parkinson maladie; Génétique; Haplotype; Chromosome X; Amine oxidase (flavin-containing); Mâle; Homme; Exploration; Facteur risque</FD>
<FG>Oxidoreductases; Enzyme; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative</FG>
<ED>Parkinson disease; Genetics; Haplotype; X-Chromosome; Amine oxidase (flavin-containing); Male; Human; Exploration; Risk factor</ED>
<EG>Oxidoreductases; Enzyme; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease</EG>
<SD>Parkinson enfermedad; Genética; Haplotipo; Cromosoma X; Amine oxidase (flavin-containing); Macho; Hombre; Exploración; Factor riesgo</SD>
<LO>INIST-20953.354000045669810030</LO>
<ID>94-0459266</ID>
</server>
</inist>
</record>
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