Intrafamilial heterogeneity of facial hyperkinesias : Chance association of tics, cranial dystonia, and huntington's disease?
Identifieur interne :
002A30 ( PascalFrancis/Corpus );
précédent :
002A29;
suivant :
002A31
Intrafamilial heterogeneity of facial hyperkinesias : Chance association of tics, cranial dystonia, and huntington's disease?
Auteurs : Jorg Müller ;
Gregor K. Wenning ;
Jorg Wissel ;
Werner PoeweSource :
-
Movement disorders [ 0885-3185 ] ; 2001.
RBID : Pascal:01-0332913
Descripteurs français
- Pascal (Inist)
- Hyperkinésie,
Face,
Tic,
Dystonie,
Chorée Huntington,
Hétérogénéité,
Phénotype,
Etude familiale,
Diagnostic différentiel,
Adulte,
Mâle.
English descriptors
- KwdEn :
- Adult,
Differential diagnostic,
Dystonia,
Face,
Family study,
Heterogeneity,
Huntington disease,
Hyperkinesia,
Male,
Phenotype,
Tic.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
A01 | 01 | 1 | | @0 0885-3185 |
---|
A03 | | 1 | | @0 Mov. disord. |
---|
A05 | | | | @2 16 |
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A06 | | | | @2 2 |
---|
A08 | 01 | 1 | ENG | @1 Intrafamilial heterogeneity of facial hyperkinesias : Chance association of tics, cranial dystonia, and huntington's disease? |
---|
A11 | 01 | 1 | | @1 MÜLLER (Jorg) |
---|
A11 | 02 | 1 | | @1 WENNING (Gregor K.) |
---|
A11 | 03 | 1 | | @1 WISSEL (Jorg) |
---|
A11 | 04 | 1 | | @1 POEWE (Werner) |
---|
A14 | 01 | | | @1 Department of Neurology, University Hospital Innsbruck @2 Innsbruck @3 AUT @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. |
---|
A20 | | | | @1 370-372 |
---|
A21 | | | | @1 2001 |
---|
A23 | 01 | | | @0 ENG |
---|
A43 | 01 | | | @1 INIST @2 20953 @5 354000096545190350 |
---|
A44 | | | | @0 0000 @1 © 2001 INIST-CNRS. All rights reserved. |
---|
A45 | | | | @0 21 ref. |
---|
A47 | 01 | 1 | | @0 01-0332913 |
---|
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 Hyperkinésie @5 01 |
---|
C03 | 01 | X | ENG | @0 Hyperkinesia @5 01 |
---|
C03 | 01 | X | SPA | @0 Hiperquinesia @5 01 |
---|
C03 | 02 | X | FRE | @0 Face @5 02 |
---|
C03 | 02 | X | ENG | @0 Face @5 02 |
---|
C03 | 02 | X | SPA | @0 Cara @5 02 |
---|
C03 | 03 | X | FRE | @0 Tic @5 04 |
---|
C03 | 03 | X | ENG | @0 Tic @5 04 |
---|
C03 | 03 | X | SPA | @0 Tic @5 04 |
---|
C03 | 04 | X | FRE | @0 Dystonie @5 07 |
---|
C03 | 04 | X | ENG | @0 Dystonia @5 07 |
---|
C03 | 04 | X | SPA | @0 Distonía @5 07 |
---|
C03 | 05 | X | FRE | @0 Chorée Huntington @5 10 |
---|
C03 | 05 | X | ENG | @0 Huntington disease @5 10 |
---|
C03 | 05 | X | SPA | @0 Corea Huntington @5 10 |
---|
C03 | 06 | X | FRE | @0 Hétérogénéité @5 13 |
---|
C03 | 06 | X | ENG | @0 Heterogeneity @5 13 |
---|
C03 | 06 | X | SPA | @0 Heterogeneidad @5 13 |
---|
C03 | 07 | X | FRE | @0 Phénotype @5 14 |
---|
C03 | 07 | X | ENG | @0 Phenotype @5 14 |
---|
C03 | 07 | X | SPA | @0 Fenotipo @5 14 |
---|
C03 | 08 | X | FRE | @0 Etude familiale @5 17 |
---|
C03 | 08 | X | ENG | @0 Family study @5 17 |
---|
C03 | 08 | X | SPA | @0 Estudio familiar @5 17 |
---|
C03 | 09 | X | FRE | @0 Diagnostic différentiel @5 18 |
---|
C03 | 09 | X | ENG | @0 Differential diagnostic @5 18 |
---|
C03 | 09 | X | SPA | @0 Diagnóstico diferencial @5 18 |
---|
C03 | 10 | X | FRE | @0 Adulte @5 20 |
---|
C03 | 10 | X | ENG | @0 Adult @5 20 |
---|
C03 | 10 | X | SPA | @0 Adulto @5 20 |
---|
C03 | 11 | X | FRE | @0 Mâle @5 21 |
---|
C03 | 11 | X | ENG | @0 Male @5 21 |
---|
C03 | 11 | X | SPA | @0 Macho @5 21 |
---|
C07 | 01 | X | FRE | @0 Homme |
---|
C07 | 01 | X | ENG | @0 Human |
---|
C07 | 01 | X | SPA | @0 Hombre |
---|
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 Trouble neurologique @5 38 |
---|
C07 | 03 | X | ENG | @0 Neurological disorder @5 38 |
---|
C07 | 03 | X | SPA | @0 Trastorno neurológico @5 38 |
---|
C07 | 04 | X | FRE | @0 Trouble psychomotricité @5 39 |
---|
C07 | 04 | X | ENG | @0 Psychomotor disorder @5 39 |
---|
C07 | 04 | X | SPA | @0 Trastorno psicomotriz @5 39 |
---|
C07 | 05 | X | FRE | @0 Mouvement involontaire @5 45 |
---|
C07 | 05 | X | ENG | @0 Involuntary movement @5 45 |
---|
C07 | 05 | X | SPA | @0 Movimiento involuntario @5 45 |
---|
C07 | 06 | X | FRE | @0 Muscle strié pathologie @5 53 |
---|
C07 | 06 | X | ENG | @0 Striated muscle disease @5 53 |
---|
C07 | 06 | X | SPA | @0 Músculo estriado patología @5 53 |
---|
C07 | 07 | X | FRE | @0 Maladie dégénérative @5 61 |
---|
C07 | 07 | X | ENG | @0 Degenerative disease @5 61 |
---|
C07 | 07 | X | SPA | @0 Enfermedad degenerativa @5 61 |
---|
C07 | 08 | X | FRE | @0 Maladie héréditaire @5 62 |
---|
C07 | 08 | X | ENG | @0 Genetic disease @5 62 |
---|
C07 | 08 | X | SPA | @0 Enfermedad hereditaria @5 62 |
---|
C07 | 09 | X | FRE | @0 Extrapyramidal syndrome @5 63 |
---|
C07 | 09 | X | ENG | @0 Extrapyramidal syndrome @5 63 |
---|
C07 | 09 | X | SPA | @0 Extrapiramidal síndrome @5 63 |
---|
N21 | | | | @1 232 |
---|
|
Format Inist (serveur)
NO : | PASCAL 01-0332913 INIST |
ET : | Intrafamilial heterogeneity of facial hyperkinesias : Chance association of tics, cranial dystonia, and huntington's disease? |
AU : | MÜLLER (Jorg); WENNING (Gregor K.); WISSEL (Jorg); POEWE (Werner) |
AF : | Department of Neurology, University Hospital Innsbruck/Innsbruck/Autriche (1 aut., 2 aut., 3 aut., 4 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2001; Vol. 16; No. 2; Pp. 370-372; Bibl. 21 ref. |
LA : | Anglais |
CC : | 002B17G |
FD : | Hyperkinésie; Face; Tic; Dystonie; Chorée Huntington; Hétérogénéité; Phénotype; Etude familiale; Diagnostic différentiel; Adulte; Mâle |
FG : | Homme; Système nerveux pathologie; Trouble neurologique; Trouble psychomotricité; Mouvement involontaire; Muscle strié pathologie; Maladie dégénérative; Maladie héréditaire; Extrapyramidal syndrome |
ED : | Hyperkinesia; Face; Tic; Dystonia; Huntington disease; Heterogeneity; Phenotype; Family study; Differential diagnostic; Adult; Male |
EG : | Human; Nervous system diseases; Neurological disorder; Psychomotor disorder; Involuntary movement; Striated muscle disease; Degenerative disease; Genetic disease; Extrapyramidal syndrome |
SD : | Hiperquinesia; Cara; Tic; Distonía; Corea Huntington; Heterogeneidad; Fenotipo; Estudio familiar; Diagnóstico diferencial; Adulto; Macho |
LO : | INIST-20953.354000096545190350 |
ID : | 01-0332913 |
Links to Exploration step
Pascal:01-0332913
Le document en format XML
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<s5>38</s5>
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<s5>39</s5>
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<s5>45</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Muscle strié pathologie</s0>
<s5>53</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Striated muscle disease</s0>
<s5>53</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Músculo estriado patología</s0>
<s5>53</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>61</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>61</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>61</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>62</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>62</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>62</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>63</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>63</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>63</s5>
</fC07>
<fN21><s1>232</s1>
</fN21>
</pA>
</standard>
<server><NO>PASCAL 01-0332913 INIST</NO>
<ET>Intrafamilial heterogeneity of facial hyperkinesias : Chance association of tics, cranial dystonia, and huntington's disease?</ET>
<AU>MÜLLER (Jorg); WENNING (Gregor K.); WISSEL (Jorg); POEWE (Werner)</AU>
<AF>Department of Neurology, University Hospital Innsbruck/Innsbruck/Autriche (1 aut., 2 aut., 3 aut., 4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2001; Vol. 16; No. 2; Pp. 370-372; Bibl. 21 ref.</SO>
<LA>Anglais</LA>
<CC>002B17G</CC>
<FD>Hyperkinésie; Face; Tic; Dystonie; Chorée Huntington; Hétérogénéité; Phénotype; Etude familiale; Diagnostic différentiel; Adulte; Mâle</FD>
<FG>Homme; Système nerveux pathologie; Trouble neurologique; Trouble psychomotricité; Mouvement involontaire; Muscle strié pathologie; Maladie dégénérative; Maladie héréditaire; Extrapyramidal syndrome</FG>
<ED>Hyperkinesia; Face; Tic; Dystonia; Huntington disease; Heterogeneity; Phenotype; Family study; Differential diagnostic; Adult; Male</ED>
<EG>Human; Nervous system diseases; Neurological disorder; Psychomotor disorder; Involuntary movement; Striated muscle disease; Degenerative disease; Genetic disease; Extrapyramidal syndrome</EG>
<SD>Hiperquinesia; Cara; Tic; Distonía; Corea Huntington; Heterogeneidad; Fenotipo; Estudio familiar; Diagnóstico diferencial; Adulto; Macho</SD>
<LO>INIST-20953.354000096545190350</LO>
<ID>01-0332913</ID>
</server>
</inist>
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