Movement Disorders (revue)

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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 Poewe

Source :

RBID : Pascal:01-0332913

Descripteurs français

English descriptors


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
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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<s0>Involuntary movement</s0>
<s5>45</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<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>
</record>

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