MovDisordV3, PascalFrancis, Corpus, bibRecord, 003226

Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone

Identifieur interne : 003226 ( PascalFrancis/Corpus ); précédent : 003225; suivant : 003227

Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone

Auteurs : J. H. Friedman

Source :

Movement disorders [ 0885-3185 ] ; 1997.

RBID : Pascal:97-0411298

Descripteurs français

Pascal (Inist)
- Joseph maladie, Hérédodégénérescence spinocérébelleuse, Buspirone, Psychotrope, Chimiothérapie, Traitement, Homme, Mâle, Etude cas.

English descriptors

KwdEn :
- Buspirone, Case study, Chemotherapy, Human, Joseph disease, Male, Psychotropic, Spinocerebellar heredodegeneration, Treatment.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0885-3185`
A03		`1`		`@0 Mov. disord.`
A05				`@2 12`
A06				`@2 4`
A08	`01`	`1`	`ENG`	`@1 Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone`
A11	`01`	`1`		`@1 FRIEDMAN (J. H.)`
A14	`01`			`@1 Memorial Hospital of Rhode Island, Dept. of Clinical Neurosciences, Brown University School of Medicine @3 USA @Z 1 aut.`
A20				`@1 613-614`
A21				`@1 1997`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000067729910250`
A44				`@0 0000 @1 © 1997 INIST-CNRS. All rights reserved.`
A45				`@0 8 ref.`
A47	`01`	`1`		`@0 97-0411298`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C02	`01`	`X`		`@0 002B02B03`
C03	`01`	`X`	`FRE`	`@0 Joseph maladie @5 01`
C03	`01`	`X`	`ENG`	`@0 Joseph disease @5 01`
C03	`01`	`X`	`SPA`	`@0 Joseph enfermedad @5 01`
C03	`02`	`X`	`FRE`	`@0 Hérédodégénérescence spinocérébelleuse @5 04`
C03	`02`	`X`	`ENG`	`@0 Spinocerebellar heredodegeneration @5 04`
C03	`02`	`X`	`SPA`	`@0 Heredodegeneración espinocerebelosa @5 04`
C03	`03`	`X`	`FRE`	`@0 Buspirone @2 NK @2 FR @5 07`
C03	`03`	`X`	`ENG`	`@0 Buspirone @2 NK @2 FR @5 07`
C03	`03`	`X`	`SPA`	`@0 Buspirona @2 NK @2 FR @5 07`
C03	`04`	`X`	`FRE`	`@0 Psychotrope @2 FX @5 08`
C03	`04`	`X`	`ENG`	`@0 Psychotropic @2 FX @5 08`
C03	`04`	`X`	`SPA`	`@0 Psicotropo @2 FX @5 08`
C03	`05`	`X`	`FRE`	`@0 Chimiothérapie @5 16`
C03	`05`	`X`	`ENG`	`@0 Chemotherapy @5 16`
C03	`05`	`X`	`SPA`	`@0 Quimioterapia @5 16`
C03	`06`	`X`	`FRE`	`@0 Traitement @5 17`
C03	`06`	`X`	`ENG`	`@0 Treatment @5 17`
C03	`06`	`X`	`GER`	`@0 Aufbereiten @5 17`
C03	`06`	`X`	`SPA`	`@0 Tratamiento @5 17`
C03	`07`	`X`	`FRE`	`@0 Homme @5 20`
C03	`07`	`X`	`ENG`	`@0 Human @5 20`
C03	`07`	`X`	`SPA`	`@0 Hombre @5 20`
C03	`08`	`X`	`FRE`	`@0 Mâle @5 21`
C03	`08`	`X`	`ENG`	`@0 Male @5 21`
C03	`08`	`X`	`SPA`	`@0 Macho @5 21`
C03	`09`	`X`	`FRE`	`@0 Etude cas @5 23`
C03	`09`	`X`	`ENG`	`@0 Case study @5 23`
C03	`09`	`X`	`SPA`	`@0 Estudio caso @5 23`
C07	`01`	`X`	`FRE`	`@0 Système nerveux pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Nervous system diseases @5 37`
C07	`01`	`X`	`SPA`	`@0 Sistema nervioso patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 38`
C07	`02`	`X`	`ENG`	`@0 Central nervous system disease @5 38`
C07	`02`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 38`
C07	`03`	`X`	`FRE`	`@0 Encéphale pathologie @5 39`
C07	`03`	`X`	`ENG`	`@0 Cerebral disorder @5 39`
C07	`03`	`X`	`SPA`	`@0 Encéfalo patología @5 39`
C07	`04`	`X`	`FRE`	`@0 Maladie dégénérative @5 40`
C07	`04`	`X`	`ENG`	`@0 Degenerative disease @5 40`
C07	`04`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 40`
C07	`05`	`X`	`FRE`	`@0 Métabolisme pathologie @5 41`
C07	`05`	`X`	`ENG`	`@0 Metabolic diseases @5 41`
C07	`05`	`X`	`SPA`	`@0 Metabolismo patología @5 41`
C07	`06`	`X`	`FRE`	`@0 Enzymopathie @5 42`
C07	`06`	`X`	`ENG`	`@0 Enzymopathy @5 42`
C07	`06`	`X`	`SPA`	`@0 Enzimopatía @5 42`
C07	`07`	`X`	`FRE`	`@0 Aminoacidopathie @5 43`
C07	`07`	`X`	`ENG`	`@0 Aminoacid disorder @5 43`
C07	`07`	`X`	`SPA`	`@0 Aminoacido alteración @5 43`
C07	`08`	`X`	`FRE`	`@0 Moelle épinière pathologie @5 47`
C07	`08`	`X`	`ENG`	`@0 Spinal cord disease @5 47`
C07	`08`	`X`	`SPA`	`@0 Médula espinal patología @5 47`
C07	`09`	`X`	`FRE`	`@0 Maladie héréditaire @5 50`
C07	`09`	`X`	`ENG`	`@0 Genetic disease @5 50`
C07	`09`	`X`	`SPA`	`@0 Enfermedad hereditaria @5 50`
N21				`@1 251`

Format Inist (serveur)

NO :	PASCAL 97-0411298 INIST
ET :	Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone
AU :	FRIEDMAN (J. H.)
AF :	Memorial Hospital of Rhode Island, Dept. of Clinical Neurosciences, Brown University School of Medicine/Etats-Unis (1 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1997; Vol. 12; No. 4; Pp. 613-614; Bibl. 8 ref.
LA :	Anglais
CC :	002B02B03
FD :	Joseph maladie; Hérédodégénérescence spinocérébelleuse; Buspirone; Psychotrope; Chimiothérapie; Traitement; Homme; Mâle; Etude cas
FG :	Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Maladie dégénérative; Métabolisme pathologie; Enzymopathie; Aminoacidopathie; Moelle épinière pathologie; Maladie héréditaire
ED :	Joseph disease; Spinocerebellar heredodegeneration; Buspirone; Psychotropic; Chemotherapy; Treatment; Human; Male; Case study
EG :	Nervous system diseases; Central nervous system disease; Cerebral disorder; Degenerative disease; Metabolic diseases; Enzymopathy; Aminoacid disorder; Spinal cord disease; Genetic disease
GD :	Aufbereiten
SD :	Joseph enfermedad; Heredodegeneración espinocerebelosa; Buspirona; Psicotropo; Quimioterapia; Tratamiento; Hombre; Macho; Estudio caso
LO :	INIST-20953.354000067729910250
ID :	97-0411298

Links to Exploration step

Pascal:97-0411298

Le document en format XML

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<fC03 i1="03" i2="X" l="ENG"><s0>Buspirone</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>07</s5>
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<fC03 i1="03" i2="X" l="SPA"><s0>Buspirona</s0>
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<s2>FR</s2>
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<fC03 i1="04" i2="X" l="FRE"><s0>Psychotrope</s0>
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<s5>08</s5>
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<fC03 i1="04" i2="X" l="ENG"><s0>Psychotropic</s0>
<s2>FX</s2>
<s5>08</s5>
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<fC03 i1="04" i2="X" l="SPA"><s0>Psicotropo</s0>
<s2>FX</s2>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Chimiothérapie</s0>
<s5>16</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Chemotherapy</s0>
<s5>16</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Quimioterapia</s0>
<s5>16</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Traitement</s0>
<s5>17</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Treatment</s0>
<s5>17</s5>
</fC03>
<fC03 i1="06" i2="X" l="GER"><s0>Aufbereiten</s0>
<s5>17</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Tratamiento</s0>
<s5>17</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Homme</s0>
<s5>20</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Human</s0>
<s5>20</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Hombre</s0>
<s5>20</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Mâle</s0>
<s5>21</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Male</s0>
<s5>21</s5>
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<fC03 i1="08" i2="X" l="SPA"><s0>Macho</s0>
<s5>21</s5>
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<s5>23</s5>
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<s5>23</s5>
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<fC03 i1="09" i2="X" l="SPA"><s0>Estudio caso</s0>
<s5>23</s5>
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<s5>37</s5>
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<s5>37</s5>
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<s5>37</s5>
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<s5>38</s5>
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<s5>38</s5>
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<s5>38</s5>
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<s5>39</s5>
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<s5>39</s5>
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<s5>40</s5>
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<fC07 i1="04" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>40</s5>
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<fC07 i1="05" i2="X" l="FRE"><s0>Métabolisme pathologie</s0>
<s5>41</s5>
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<fC07 i1="05" i2="X" l="ENG"><s0>Metabolic diseases</s0>
<s5>41</s5>
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<fC07 i1="05" i2="X" l="SPA"><s0>Metabolismo patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Enzymopathie</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Enzymopathy</s0>
<s5>42</s5>
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<fC07 i1="06" i2="X" l="SPA"><s0>Enzimopatía</s0>
<s5>42</s5>
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<fC07 i1="07" i2="X" l="FRE"><s0>Aminoacidopathie</s0>
<s5>43</s5>
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<fC07 i1="07" i2="X" l="ENG"><s0>Aminoacid disorder</s0>
<s5>43</s5>
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<fC07 i1="07" i2="X" l="SPA"><s0>Aminoacido alteración</s0>
<s5>43</s5>
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<fC07 i1="08" i2="X" l="FRE"><s0>Moelle épinière pathologie</s0>
<s5>47</s5>
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<fC07 i1="08" i2="X" l="ENG"><s0>Spinal cord disease</s0>
<s5>47</s5>
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<s5>47</s5>
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<s5>50</s5>
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<s5>50</s5>
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<server><NO>PASCAL 97-0411298 INIST</NO>
<ET>Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone</ET>
<AU>FRIEDMAN (J. H.)</AU>
<AF>Memorial Hospital of Rhode Island, Dept. of Clinical Neurosciences, Brown University School of Medicine/Etats-Unis (1 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1997; Vol. 12; No. 4; Pp. 613-614; Bibl. 8 ref.</SO>
<LA>Anglais</LA>
<CC>002B02B03</CC>
<FD>Joseph maladie; Hérédodégénérescence spinocérébelleuse; Buspirone; Psychotrope; Chimiothérapie; Traitement; Homme; Mâle; Etude cas</FD>
<FG>Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Maladie dégénérative; Métabolisme pathologie; Enzymopathie; Aminoacidopathie; Moelle épinière pathologie; Maladie héréditaire</FG>
<ED>Joseph disease; Spinocerebellar heredodegeneration; Buspirone; Psychotropic; Chemotherapy; Treatment; Human; Male; Case study</ED>
<EG>Nervous system diseases; Central nervous system disease; Cerebral disorder; Degenerative disease; Metabolic diseases; Enzymopathy; Aminoacid disorder; Spinal cord disease; Genetic disease</EG>
<GD>Aufbereiten</GD>
<SD>Joseph enfermedad; Heredodegeneración espinocerebelosa; Buspirona; Psicotropo; Quimioterapia; Tratamiento; Hombre; Macho; Estudio caso</SD>
<LO>INIST-20953.354000067729910250</LO>
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   |texte=   Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone
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	Movement Disorders (revue)
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Movement Disorders (revue)

Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone

Machado-Joseph disease/spinocerebellar ataxia 3 responsive to buspirone

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