MovDisordV3, PascalFrancis, Corpus, bibRecord, 003513

Case 1, 1995 : psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction

Identifieur interne : 003513 ( PascalFrancis/Corpus ); précédent : 003512; suivant : 003514

Case 1, 1995 : psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction

Auteurs : L. M. Shulman ; A. E. Lang ; J. Jankovic ; N. J. David ; W. J. Weiner

Source :

Movement disorders [ 0885-3185 ] ; 1995.

RBID : Pascal:95-0362292

Descripteurs français

Pascal (Inist)
- Sphingolipidose héréditaire Niemann Pick, Démence, Chorée syndrome, Ataxie, Ophtalmoplégie supranucléaire, Etude cas, Symptomatologie, Homme, Mâle, Enzymopathie, Lipide.

English descriptors

KwdEn :
- Ataxia, Case study, Chorea, Dementia, Enzymopathy, Human, Lipids, Male, Niemann Pick disease, Supranuclear ophthalmoplegia, Symptomatology.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A11	`01`	`1`		`@1 SHULMAN (L. M.)`
A11	`02`	`1`		`@1 LANG (A. E.)`
A11	`03`	`1`		`@1 JANKOVIC (J.)`
A11	`04`	`1`		`@1 DAVID (N. J.)`
A11	`05`	`1`		`@1 WEINER (W. J.)`
A14	`01`			`@1 Univ. Miami school medicine, dep. neurology @2 Miami FL @3 USA @Z 1 aut. @Z 4 aut. @Z 5 aut.`
A20				`@1 257-262`
A21				`@1 1995`
A23	`01`			`@0 ENG`
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C02	`01`	`X`		`@0 002B22D02`
C03	`01`	`X`	`FRE`	`@0 Sphingolipidose héréditaire Niemann Pick @5 01`
C03	`01`	`X`	`ENG`	`@0 Niemann Pick disease @5 01`
C03	`01`	`X`	`SPA`	`@0 Esfingolipidosis hereditaria Niemann Pick @5 01`
C03	`02`	`X`	`FRE`	`@0 Démence @5 04`
C03	`02`	`X`	`ENG`	`@0 Dementia @5 04`
C03	`02`	`X`	`SPA`	`@0 Demencia @5 04`
C03	`03`	`X`	`FRE`	`@0 Chorée syndrome @5 07`
C03	`03`	`X`	`ENG`	`@0 Chorea @5 07`
C03	`03`	`X`	`SPA`	`@0 Corea síndrome @5 07`
C03	`04`	`X`	`FRE`	`@0 Ataxie @5 10`
C03	`04`	`X`	`ENG`	`@0 Ataxia @5 10`
C03	`04`	`X`	`SPA`	`@0 Ataxia @5 10`
C03	`05`	`X`	`FRE`	`@0 Ophtalmoplégie supranucléaire @5 13`
C03	`05`	`X`	`ENG`	`@0 Supranuclear ophthalmoplegia @5 13`
C03	`05`	`X`	`SPA`	`@0 Oftalmoplejía supranuclear @5 13`
C03	`06`	`X`	`FRE`	`@0 Etude cas @5 16`
C03	`06`	`X`	`ENG`	`@0 Case study @5 16`
C03	`06`	`X`	`SPA`	`@0 Estudio caso @5 16`
C03	`07`	`X`	`FRE`	`@0 Symptomatologie @5 17`
C03	`07`	`X`	`ENG`	`@0 Symptomatology @5 17`
C03	`07`	`X`	`SPA`	`@0 Sintomatología @5 17`
C03	`08`	`X`	`FRE`	`@0 Homme @5 20`
C03	`08`	`X`	`ENG`	`@0 Human @5 20`
C03	`08`	`X`	`SPA`	`@0 Hombre @5 20`
C03	`09`	`X`	`FRE`	`@0 Mâle @5 21`
C03	`09`	`X`	`ENG`	`@0 Male @5 21`
C03	`09`	`X`	`SPA`	`@0 Macho @5 21`
C03	`10`	`X`	`FRE`	`@0 Enzymopathie @5 25`
C03	`10`	`X`	`ENG`	`@0 Enzymopathy @5 25`
C03	`10`	`X`	`SPA`	`@0 Enzimopatía @5 25`
C03	`11`	`X`	`FRE`	`@0 Lipide @5 26`
C03	`11`	`X`	`ENG`	`@0 Lipids @5 26`
C03	`11`	`X`	`SPA`	`@0 Lípido @5 26`
C07	`01`	`X`	`FRE`	`@0 Métabolisme pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Metabolic diseases @5 37`
C07	`01`	`X`	`SPA`	`@0 Metabolismo patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Lipoïdose @5 38`
C07	`02`	`X`	`ENG`	`@0 Lipoidosis @5 38`
C07	`02`	`X`	`SPA`	`@0 Lipoidosis @5 38`
C07	`03`	`X`	`FRE`	`@0 Système nerveux pathologie @5 39`
C07	`03`	`X`	`ENG`	`@0 Nervous system diseases @5 39`
C07	`03`	`X`	`SPA`	`@0 Sistema nervioso patología @5 39`
C07	`04`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 40`
C07	`04`	`X`	`ENG`	`@0 Central nervous system disease @5 40`
C07	`04`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 40`
C07	`05`	`X`	`FRE`	`@0 Encéphale pathologie @5 41`
C07	`05`	`X`	`ENG`	`@0 Cerebral disorder @5 41`
C07	`05`	`X`	`SPA`	`@0 Encéfalo patología @5 41`
C07	`06`	`X`	`FRE`	`@0 Maladie héréditaire @5 42`
C07	`06`	`X`	`ENG`	`@0 Genetic disease @5 42`
C07	`06`	`X`	`SPA`	`@0 Enfermedad hereditaria @5 42`
C07	`07`	`X`	`FRE`	`@0 Trouble neurologique @5 56`
C07	`07`	`X`	`ENG`	`@0 Neurological disorder @5 56`
C07	`07`	`X`	`SPA`	`@0 Trastorno neurológico @5 56`
C07	`08`	`X`	`FRE`	`@0 Mouvement involontaire @5 57`
C07	`08`	`X`	`ENG`	`@0 Involuntary movement @5 57`
C07	`08`	`X`	`SPA`	`@0 Movimiento involuntario @5 57`
C07	`09`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 58`
C07	`09`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 58`
C07	`09`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 58`
C07	`10`	`X`	`FRE`	`@0 Oeil pathologie @5 69`
C07	`10`	`X`	`ENG`	`@0 Eye disease @5 69`
C07	`10`	`X`	`SPA`	`@0 Ojo patología @5 69`
C07	`11`	`X`	`FRE`	`@0 Oculomotricité syndrome @5 70`
C07	`11`	`X`	`ENG`	`@0 Oculomotor syndrome @5 70`
C07	`11`	`X`	`SPA`	`@0 Oculomotricidad síndrome @5 70`
C07	`12`	`X`	`FRE`	`@0 Tronc cérébral syndrome @5 73`
C07	`12`	`X`	`ENG`	`@0 Brain stem syndrome @5 73`
C07	`12`	`X`	`SPA`	`@0 Tallo encefalico sindrome @5 73`
C07	`13`	`X`	`FRE`	`@0 Maladie dégénérative @5 75`
C07	`13`	`X`	`ENG`	`@0 Degenerative disease @5 75`
C07	`13`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 75`
N21				`@1 205`

Format Inist (serveur)

NO :	PASCAL 95-0362292 INIST
ET :	Case 1, 1995 : psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction
AU :	SHULMAN (L. M.); LANG (A. E.); JANKOVIC (J.); DAVID (N. J.); WEINER (W. J.)
AF :	Univ. Miami school medicine, dep. neurology/Miami FL/Etats-Unis (1 aut., 4 aut., 5 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1995; Vol. 10; No. 3; Pp. 257-262; Bibl. 42 ref.
LA :	Anglais
CC :	002B22D02
FD :	Sphingolipidose héréditaire Niemann Pick; Démence; Chorée syndrome; Ataxie; Ophtalmoplégie supranucléaire; Etude cas; Symptomatologie; Homme; Mâle; Enzymopathie; Lipide
FG :	Métabolisme pathologie; Lipoïdose; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Maladie héréditaire; Trouble neurologique; Mouvement involontaire; Extrapyramidal syndrome; Oeil pathologie; Oculomotricité syndrome; Tronc cérébral syndrome; Maladie dégénérative
ED :	Niemann Pick disease; Dementia; Chorea; Ataxia; Supranuclear ophthalmoplegia; Case study; Symptomatology; Human; Male; Enzymopathy; Lipids
EG :	Metabolic diseases; Lipoidosis; Nervous system diseases; Central nervous system disease; Cerebral disorder; Genetic disease; Neurological disorder; Involuntary movement; Extrapyramidal syndrome; Eye disease; Oculomotor syndrome; Brain stem syndrome; Degenerative disease
SD :	Esfingolipidosis hereditaria Niemann Pick; Demencia; Corea síndrome; Ataxia; Oftalmoplejía supranuclear; Estudio caso; Sintomatología; Hombre; Macho; Enzimopatía; Lípido
LO :	INIST-20953.354000050919630030
ID :	95-0362292

Links to Exploration step

Pascal:95-0362292

Le document en format XML

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<s5>25</s5>
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<fC03 i1="10" i2="X" l="ENG"><s0>Enzymopathy</s0>
<s5>25</s5>
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<s5>25</s5>
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<s5>26</s5>
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<s5>26</s5>
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<s5>26</s5>
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<fC07 i1="01" i2="X" l="FRE"><s0>Métabolisme pathologie</s0>
<s5>37</s5>
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<s5>37</s5>
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<fC07 i1="01" i2="X" l="SPA"><s0>Metabolismo patología</s0>
<s5>37</s5>
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<fC07 i1="02" i2="X" l="FRE"><s0>Lipoïdose</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Lipoidosis</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Lipoidosis</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>56</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>56</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>56</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Mouvement involontaire</s0>
<s5>57</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Involuntary movement</s0>
<s5>57</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Movimiento involuntario</s0>
<s5>57</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>58</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>58</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>58</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Oeil pathologie</s0>
<s5>69</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Eye disease</s0>
<s5>69</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Ojo patología</s0>
<s5>69</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Oculomotricité syndrome</s0>
<s5>70</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Oculomotor syndrome</s0>
<s5>70</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA"><s0>Oculomotricidad síndrome</s0>
<s5>70</s5>
</fC07>
<fC07 i1="12" i2="X" l="FRE"><s0>Tronc cérébral syndrome</s0>
<s5>73</s5>
</fC07>
<fC07 i1="12" i2="X" l="ENG"><s0>Brain stem syndrome</s0>
<s5>73</s5>
</fC07>
<fC07 i1="12" i2="X" l="SPA"><s0>Tallo encefalico sindrome</s0>
<s5>73</s5>
</fC07>
<fC07 i1="13" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>75</s5>
</fC07>
<fC07 i1="13" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>75</s5>
</fC07>
<fC07 i1="13" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>75</s5>
</fC07>
<fN21><s1>205</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 95-0362292 INIST</NO>
<ET>Case 1, 1995 : psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction</ET>
<AU>SHULMAN (L. M.); LANG (A. E.); JANKOVIC (J.); DAVID (N. J.); WEINER (W. J.)</AU>
<AF>Univ. Miami school medicine, dep. neurology/Miami FL/Etats-Unis (1 aut., 4 aut., 5 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1995; Vol. 10; No. 3; Pp. 257-262; Bibl. 42 ref.</SO>
<LA>Anglais</LA>
<CC>002B22D02</CC>
<FD>Sphingolipidose héréditaire Niemann Pick; Démence; Chorée syndrome; Ataxie; Ophtalmoplégie supranucléaire; Etude cas; Symptomatologie; Homme; Mâle; Enzymopathie; Lipide</FD>
<FG>Métabolisme pathologie; Lipoïdose; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Maladie héréditaire; Trouble neurologique; Mouvement involontaire; Extrapyramidal syndrome; Oeil pathologie; Oculomotricité syndrome; Tronc cérébral syndrome; Maladie dégénérative</FG>
<ED>Niemann Pick disease; Dementia; Chorea; Ataxia; Supranuclear ophthalmoplegia; Case study; Symptomatology; Human; Male; Enzymopathy; Lipids</ED>
<EG>Metabolic diseases; Lipoidosis; Nervous system diseases; Central nervous system disease; Cerebral disorder; Genetic disease; Neurological disorder; Involuntary movement; Extrapyramidal syndrome; Eye disease; Oculomotor syndrome; Brain stem syndrome; Degenerative disease</EG>
<SD>Esfingolipidosis hereditaria Niemann Pick; Demencia; Corea síndrome; Ataxia; Oftalmoplejía supranuclear; Estudio caso; Sintomatología; Hombre; Macho; Enzimopatía; Lípido</SD>
<LO>INIST-20953.354000050919630030</LO>
<ID>95-0362292</ID>
</server>
</inist>
</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Case 1, 1995 : psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction

Case 1, 1995 : psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction

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