MovDisordV3, PascalFrancis, Corpus, bibRecord, 003552

Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy

Identifieur interne : 003552 ( PascalFrancis/Corpus ); précédent : 003551; suivant : 003553

Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy

Auteurs : XIAO-HUI ZHONG ; J. W. Haycock ; K. Shannak ; Y. Robitaille ; J. Fratkin ; A. H. Koeppen ; O. Hornykiewicz ; S. J. Kish

Source :

Movement disorders [ 0885-3185 ] ; 1995.

RBID : Pascal:95-0167513

Descripteurs français

Pascal (Inist)
- Parkinson maladie, Atrophie, Olivopontocérébelleux, Corps strié, Tyrosine 3-monooxygenase, Aromatic-L-amino-acid decarboxylase, Etude comparative, Exploration, Homme.

English descriptors

KwdEn :
- Aromatic-L-amino-acid decarboxylase, Atrophia, Comparative study, Corpus striatum, Exploration, Human, Olivopontocerebellar, Parkinson disease, Tyrosine 3-monooxygenase.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 10`
A06				`@2 1`
A08	`01`	`1`	`ENG`	`@1 Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy`
A11	`01`	`1`		`@1 XIAO-HUI ZHONG`
A11	`02`	`1`		`@1 HAYCOCK (J. W.)`
A11	`03`	`1`		`@1 SHANNAK (K.)`
A11	`04`	`1`		`@1 ROBITAILLE (Y.)`
A11	`05`	`1`		`@1 FRATKIN (J.)`
A11	`06`	`1`		`@1 KOEPPEN (A. H.)`
A11	`07`	`1`		`@1 HORNYKIEWICZ (O.)`
A11	`08`	`1`		`@1 KISH (S. J.)`
A14	`01`			`@1 Clarke inst. psychiatry, human neurochemical pathology lab. @2 Toronto ON M5T 1R8 @3 CAN @Z 1 aut. @Z 3 aut. @Z 7 aut. @Z 8 aut.`
A20				`@1 10-17`
A21				`@1 1995`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000058100400020`
A44				`@0 0000`
A45				`@0 26 ref.`
A47	`01`	`1`		`@0 95-0167513`
A60				`@1 P`
A61				`@0 A`
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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 Atrophie @5 04`
C03	`02`	`X`	`ENG`	`@0 Atrophia @5 04`
C03	`02`	`X`	`SPA`	`@0 Atrofia @5 04`
C03	`03`	`X`	`FRE`	`@0 Olivopontocérébelleux @5 05`
C03	`03`	`X`	`ENG`	`@0 Olivopontocerebellar @5 05`
C03	`03`	`X`	`SPA`	`@0 Olivopontocerebeloso @5 05`
C03	`04`	`X`	`FRE`	`@0 Corps strié @5 07`
C03	`04`	`X`	`ENG`	`@0 Corpus striatum @5 07`
C03	`04`	`X`	`SPA`	`@0 Cuerpo estriado @5 07`
C03	`05`	`X`	`FRE`	`@0 Tyrosine 3-monooxygenase @2 FE @5 10 @6 Tyrosine «3»-monooxygenase`
C03	`05`	`X`	`ENG`	`@0 Tyrosine 3-monooxygenase @2 FE @5 10 @6 Tyrosine «3»-monooxygenase`
C03	`05`	`X`	`SPA`	`@0 Tyrosine 3-monooxygenase @2 FE @5 10 @6 Tyrosine «3»-monooxygenase`
C03	`06`	`X`	`FRE`	`@0 Aromatic-L-amino-acid decarboxylase @2 FE @5 11 @6 Aromatic-«L»-amino-acid decarboxylase`
C03	`06`	`X`	`ENG`	`@0 Aromatic-L-amino-acid decarboxylase @2 FE @5 11 @6 Aromatic-«L»-amino-acid decarboxylase`
C03	`06`	`X`	`SPA`	`@0 Aromatic-L-amino-acid decarboxylase @2 FE @5 11 @6 Aromatic-«L»-amino-acid decarboxylase`
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`
C07	`01`	`X`	`FRE`	`@0 Oxidoreductases @2 FE`
C07	`01`	`X`	`ENG`	`@0 Oxidoreductases @2 FE`
C07	`01`	`X`	`SPA`	`@0 Oxidoreductases @2 FE`
C07	`02`	`X`	`FRE`	`@0 Enzyme`
C07	`02`	`X`	`ENG`	`@0 Enzyme`
C07	`02`	`X`	`SPA`	`@0 Enzima`
C07	`03`	`X`	`FRE`	`@0 Carboxy-lyases @2 FE`
C07	`03`	`X`	`ENG`	`@0 Carboxy-lyases @2 FE`
C07	`03`	`X`	`SPA`	`@0 Carboxy-lyases @2 FE`
C07	`04`	`X`	`FRE`	`@0 Carbon-carbon lyases @2 FE`
C07	`04`	`X`	`ENG`	`@0 Carbon-carbon lyases @2 FE`
C07	`04`	`X`	`SPA`	`@0 Carbon-carbon lyases @2 FE`
C07	`05`	`X`	`FRE`	`@0 Lyases @2 FE`
C07	`05`	`X`	`ENG`	`@0 Lyases @2 FE`
C07	`05`	`X`	`SPA`	`@0 Lyases @2 FE`
C07	`06`	`X`	`FRE`	`@0 Système nerveux pathologie @5 37`
C07	`06`	`X`	`ENG`	`@0 Nervous system diseases @5 37`
C07	`06`	`X`	`SPA`	`@0 Sistema nervioso patología @5 37`
C07	`07`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 38`
C07	`07`	`X`	`ENG`	`@0 Central nervous system disease @5 38`
C07	`07`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 38`
C07	`08`	`X`	`FRE`	`@0 Encéphale pathologie @5 39`
C07	`08`	`X`	`ENG`	`@0 Cerebral disorder @5 39`
C07	`08`	`X`	`SPA`	`@0 Encéfalo patología @5 39`
C07	`09`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 40`
C07	`09`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 40`
C07	`09`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 40`
C07	`10`	`X`	`FRE`	`@0 Maladie dégénérative @5 41`
C07	`10`	`X`	`ENG`	`@0 Degenerative disease @5 41`
C07	`10`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 41`
C07	`11`	`X`	`FRE`	`@0 Maladie héréditaire @5 45`
C07	`11`	`X`	`ENG`	`@0 Genetic disease @5 45`
C07	`11`	`X`	`SPA`	`@0 Enfermedad hereditaria @5 45`
N21				`@1 095`

Format Inist (serveur)

NO :	PASCAL 95-0167513 INIST
ET :	Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy
AU :	XIAO-HUI ZHONG; HAYCOCK (J. W.); SHANNAK (K.); ROBITAILLE (Y.); FRATKIN (J.); KOEPPEN (A. H.); HORNYKIEWICZ (O.); KISH (S. J.)
AF :	Clarke inst. psychiatry, human neurochemical pathology lab./Toronto ON M5T 1R8/Canada (1 aut., 3 aut., 7 aut., 8 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1995; Vol. 10; No. 1; Pp. 10-17; Bibl. 26 ref.
LA :	Anglais
CC :	002B17G
FD :	Parkinson maladie; Atrophie; Olivopontocérébelleux; Corps strié; Tyrosine 3-monooxygenase; Aromatic-L-amino-acid decarboxylase; Etude comparative; Exploration; Homme
FG :	Oxidoreductases; Enzyme; Carboxy-lyases; Carbon-carbon lyases; Lyases; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Maladie héréditaire
ED :	Parkinson disease; Atrophia; Olivopontocerebellar; Corpus striatum; Tyrosine 3-monooxygenase; Aromatic-L-amino-acid decarboxylase; Comparative study; Exploration; Human
EG :	Oxidoreductases; Enzyme; Carboxy-lyases; Carbon-carbon lyases; Lyases; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease
GD :	Vergleich
SD :	Parkinson enfermedad; Atrofia; Olivopontocerebeloso; Cuerpo estriado; Tyrosine 3-monooxygenase; Aromatic-L-amino-acid decarboxylase; Estudio comparativo; Exploración; Hombre
LO :	INIST-20953.354000058100400020
ID :	95-0167513

Links to Exploration step

Pascal:95-0167513

Le document en format XML

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<fC03 i1="06" i2="X" l="FRE"><s0>Aromatic-L-amino-acid decarboxylase</s0>
<s2>FE</s2>
<s5>11</s5>
<s6>Aromatic-«L»-amino-acid decarboxylase</s6>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Aromatic-L-amino-acid decarboxylase</s0>
<s2>FE</s2>
<s5>11</s5>
<s6>Aromatic-«L»-amino-acid decarboxylase</s6>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Aromatic-L-amino-acid decarboxylase</s0>
<s2>FE</s2>
<s5>11</s5>
<s6>Aromatic-«L»-amino-acid decarboxylase</s6>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Etude comparative</s0>
<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>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Human</s0>
<s5>20</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Hombre</s0>
<s5>20</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>Carboxy-lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Carboxy-lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Carboxy-lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Carbon-carbon lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Carbon-carbon lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Carbon-carbon lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Lyases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>45</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>45</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>45</s5>
</fC07>
<fN21><s1>095</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 95-0167513 INIST</NO>
<ET>Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy</ET>
<AU>XIAO-HUI ZHONG; HAYCOCK (J. W.); SHANNAK (K.); ROBITAILLE (Y.); FRATKIN (J.); KOEPPEN (A. H.); HORNYKIEWICZ (O.); KISH (S. J.)</AU>
<AF>Clarke inst. psychiatry, human neurochemical pathology lab./Toronto ON M5T 1R8/Canada (1 aut., 3 aut., 7 aut., 8 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1995; Vol. 10; No. 1; Pp. 10-17; Bibl. 26 ref.</SO>
<LA>Anglais</LA>
<CC>002B17G</CC>
<FD>Parkinson maladie; Atrophie; Olivopontocérébelleux; Corps strié; Tyrosine 3-monooxygenase; Aromatic-L-amino-acid decarboxylase; Etude comparative; Exploration; Homme</FD>
<FG>Oxidoreductases; Enzyme; Carboxy-lyases; Carbon-carbon lyases; Lyases; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Maladie héréditaire</FG>
<ED>Parkinson disease; Atrophia; Olivopontocerebellar; Corpus striatum; Tyrosine 3-monooxygenase; Aromatic-L-amino-acid decarboxylase; Comparative study; Exploration; Human</ED>
<EG>Oxidoreductases; Enzyme; Carboxy-lyases; Carbon-carbon lyases; Lyases; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease</EG>
<GD>Vergleich</GD>
<SD>Parkinson enfermedad; Atrofia; Olivopontocerebeloso; Cuerpo estriado; Tyrosine 3-monooxygenase; Aromatic-L-amino-acid decarboxylase; Estudio comparativo; Exploración; Hombre</SD>
<LO>INIST-20953.354000058100400020</LO>
<ID>95-0167513</ID>
</server>
</inist>
</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy

Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy

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