MovDisordV3, PascalFrancis, Curation, bibRecord, 003692

Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family

Identifieur interne : 003692 ( PascalFrancis/Curation ); précédent : 003691; suivant : 003693

Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family

Auteurs : B. Leube [Allemagne] ; K. R. Kessler [Allemagne] ; T. Goecke [Allemagne] ; G. Auburger [Allemagne] ; R. Benecke [Allemagne]

Source :

Movement disorders [ 0885-3185 ] ; 1997.

RBID : Pascal:98-0015580

Descripteurs français

Pascal (Inist)
- Dystonie, Torsion, Idiopathique, Liaison génétique, Variabilité génétique, Etude familiale, Exploration, Homme.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Dystonia, Exploration, Family study, Genetic variability, Human, Idiopathic, Linkage, Torsion.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 12`
A06				`@2 6`
A08	`01`	`1`	`ENG`	`@1 Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family`
A11	`01`	`1`		`@1 LEUBE (B.)`
A11	`02`	`1`		`@1 KESSLER (K. R.)`
A11	`03`	`1`		`@1 GOECKE (T.)`
A11	`04`	`1`		`@1 AUBURGER (G.)`
A11	`05`	`1`		`@1 BENECKE (R.)`
A14	`01`			`@1 Department of Neurology, Heinrich-Heine-Universitat @2 Düsseldorf @3 DEU @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 5 aut.`
A14	`02`			`@1 Institute of Human Genetics and Anthropology, Heinrich-Heine-Universitat @2 Düsseldorf @3 DEU @Z 3 aut.`
A20				`@1 1000-1006`
A21				`@1 1997`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000069474290230`
A44				`@0 0000 @1 © 1997 INIST-CNRS. All rights reserved.`
A45				`@0 32 ref.`
A47	`01`	`1`		`@0 98-0015580`
A60				`@1 P`
A61				`@0 A`
A64		`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C02	`01`	`X`		`@0 002B17A01`
C03	`01`	`X`	`FRE`	`@0 Dystonie @5 01`
C03	`01`	`X`	`ENG`	`@0 Dystonia @5 01`
C03	`01`	`X`	`SPA`	`@0 Distonía @5 01`
C03	`02`	`X`	`FRE`	`@0 Torsion @5 02`
C03	`02`	`X`	`ENG`	`@0 Torsion @5 02`
C03	`02`	`X`	`GER`	`@0 Torsion @5 02`
C03	`02`	`X`	`SPA`	`@0 Torsión @5 02`
C03	`03`	`X`	`FRE`	`@0 Idiopathique @5 03`
C03	`03`	`X`	`ENG`	`@0 Idiopathic @5 03`
C03	`03`	`X`	`SPA`	`@0 Idiopático @5 03`
C03	`04`	`X`	`FRE`	`@0 Liaison génétique @5 04`
C03	`04`	`X`	`ENG`	`@0 Linkage @5 04`
C03	`04`	`X`	`SPA`	`@0 Ligamiento genético @5 04`
C03	`05`	`X`	`FRE`	`@0 Variabilité génétique @5 07`
C03	`05`	`X`	`ENG`	`@0 Genetic variability @5 07`
C03	`05`	`X`	`SPA`	`@0 Variabilidad genética @5 07`
C03	`06`	`X`	`FRE`	`@0 Etude familiale @5 16`
C03	`06`	`X`	`ENG`	`@0 Family study @5 16`
C03	`06`	`X`	`SPA`	`@0 Estudio familiar @5 16`
C03	`07`	`X`	`FRE`	`@0 Exploration @5 17`
C03	`07`	`X`	`ENG`	`@0 Exploration @5 17`
C03	`07`	`X`	`SPA`	`@0 Exploración @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`
C07	`01`	`X`	`FRE`	`@0 Muscle strié pathologie @5 37`
C07	`01`	`X`	`ENG`	`@0 Striated muscle disease @5 37`
C07	`01`	`X`	`SPA`	`@0 Músculo estriado patología @5 37`
C07	`02`	`X`	`FRE`	`@0 Système nerveux pathologie @5 38`
C07	`02`	`X`	`ENG`	`@0 Nervous system diseases @5 38`
C07	`02`	`X`	`SPA`	`@0 Sistema nervioso patología @5 38`
C07	`03`	`X`	`FRE`	`@0 Trouble neurologique @5 39`
C07	`03`	`X`	`ENG`	`@0 Neurological disorder @5 39`
C07	`03`	`X`	`SPA`	`@0 Trastorno neurológico @5 39`
C07	`04`	`X`	`FRE`	`@0 Mouvement involontaire @5 40`
C07	`04`	`X`	`ENG`	`@0 Involuntary movement @5 40`
C07	`04`	`X`	`SPA`	`@0 Movimiento involuntario @5 40`
C07	`05`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 41`
C07	`05`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 41`
C07	`05`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 41`
C07	`06`	`X`	`FRE`	`@0 Génétique @5 45`
C07	`06`	`X`	`ENG`	`@0 Genetics @5 45`
C07	`06`	`X`	`SPA`	`@0 Genética @5 45`
N21				`@1 364`

Links toward previous steps (curation, corpus...)

to stream PascalFrancis, to step Corpus: Pour aller vers cette notice dans l'étape Curation :003132

Links to Exploration step

Pascal:98-0015580

Le document en format XML

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<author><name sortKey="Leube, B" sort="Leube, B" uniqKey="Leube B" first="B." last="Leube">B. Leube</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Heinrich-Heine-Universitat</s1>
<s2>Düsseldorf</s2>
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<country>Allemagne</country>
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<author><name sortKey="Kessler, K R" sort="Kessler, K R" uniqKey="Kessler K" first="K. R." last="Kessler">K. R. Kessler</name>
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<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Institute of Human Genetics and Anthropology, Heinrich-Heine-Universitat</s1>
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<author><name sortKey="Auburger, G" sort="Auburger, G" uniqKey="Auburger G" first="G." last="Auburger">G. Auburger</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Heinrich-Heine-Universitat</s1>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family</title>
<author><name sortKey="Leube, B" sort="Leube, B" uniqKey="Leube B" first="B." last="Leube">B. Leube</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Heinrich-Heine-Universitat</s1>
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<author><name sortKey="Kessler, K R" sort="Kessler, K R" uniqKey="Kessler K" first="K. R." last="Kessler">K. R. Kessler</name>
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<author><name sortKey="Goecke, T" sort="Goecke, T" uniqKey="Goecke T" first="T." last="Goecke">T. Goecke</name>
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</author>
<author><name sortKey="Benecke, R" sort="Benecke, R" uniqKey="Benecke R" first="R." last="Benecke">R. Benecke</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Heinrich-Heine-Universitat</s1>
<s2>Düsseldorf</s2>
<s3>DEU</s3>
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<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
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<term>Exploration</term>
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<term>Torsion</term>
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<term>Torsion</term>
<term>Idiopathique</term>
<term>Liaison génétique</term>
<term>Variabilité génétique</term>
<term>Etude familiale</term>
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<s5>07</s5>
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<fC03 i1="06" i2="X" l="FRE"><s0>Etude familiale</s0>
<s5>16</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Family study</s0>
<s5>16</s5>
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<fC03 i1="06" i2="X" l="SPA"><s0>Estudio familiar</s0>
<s5>16</s5>
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<fC03 i1="07" i2="X" l="FRE"><s0>Exploration</s0>
<s5>17</s5>
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<fC03 i1="07" i2="X" l="ENG"><s0>Exploration</s0>
<s5>17</s5>
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<fC03 i1="07" i2="X" l="SPA"><s0>Exploración</s0>
<s5>17</s5>
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<s5>20</s5>
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<s5>20</s5>
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<s5>37</s5>
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<s5>37</s5>
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<s5>40</s5>
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<s5>45</s5>
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<s5>45</s5>
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<fC07 i1="06" i2="X" l="SPA"><s0>Genética</s0>
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   |type=    RBID
   |clé=     Pascal:98-0015580
   |texte=   Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family
}}

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	Movement Disorders (revue)
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Movement Disorders (revue)

Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family

Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family

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