MovDisordV3, PascalFrancis, Corpus, bibRecord, 002695

Tremor/ataxia syndrome in fragile X carrier males

Identifieur interne : 002695 ( PascalFrancis/Corpus ); précédent : 002694; suivant : 002696

Tremor/ataxia syndrome in fragile X carrier males

Auteurs : Maureen A. Leehey ; Randi J. Hagerman ; William M. Landau ; Jim Grigsby ; Flora Tassone ; Paul J. Hagerman

Source :

Movement disorders [ 0885-3185 ] ; 2002.

RBID : Pascal:02-0456862

Descripteurs français

Pascal (Inist)
- X fragile syndrome, Tremblement, Ataxie, Phénotype, Etude cas, Diagnostic, Déterminisme génétique, Personne âgée, Mâle, Prémutation.

English descriptors

KwdEn :
- Ataxia, Case study, Diagnosis, Elderly, Fragile X syndrome, Genetic determinism, Male, Phenotype, Premutation, Tremor.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 17`
A06				`@2 4`
A08	`01`	`1`	`ENG`	`@1 Tremor/ataxia syndrome in fragile X carrier males`
A11	`01`	`1`		`@1 LEEHEY (Maureen A.)`
A11	`02`	`1`		`@1 HAGERMAN (Randi J.)`
A11	`03`	`1`		`@1 LANDAU (William M.)`
A11	`04`	`1`		`@1 GRIGSBY (Jim)`
A11	`05`	`1`		`@1 TASSONE (Flora)`
A11	`06`	`1`		`@1 HAGERMAN (Paul J.)`
A14	`01`			`@1 Department of Neurology, University of Colorado Health Sciences Center @2 Denver, Colorado @3 USA @Z 1 aut.`
A14	`02`			`@1 M.I.N.D. Institute, University of California at Davis Medical Center @2 Sacramento, California @3 USA @Z 2 aut.`
A14	`03`			`@1 Department of Neurology, Washington University School of Medicine @2 Saint Louis, Missouri @3 USA @Z 3 aut.`
A14	`04`			`@1 Department of Medicine, University of Colorado Health Sciences Center @2 Denver, Colorado @3 USA @Z 4 aut.`
A14	`05`			`@1 Department of Biological Chemistry, University of California at Davis School of Medicine @2 Davis, California @3 USA @Z 5 aut. @Z 6 aut.`
A20				`@1 744-745`
A21				`@1 2002`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000108922560170`
A44				`@0 0000 @1 © 2002 INIST-CNRS. All rights reserved.`
A45				`@0 8 ref.`
A47	`01`	`1`		`@0 02-0456862`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C02	`01`	`X`		`@0 002B23E`
C03	`01`	`X`	`FRE`	`@0 X fragile syndrome @5 01`
C03	`01`	`X`	`ENG`	`@0 Fragile X syndrome @5 01`
C03	`01`	`X`	`SPA`	`@0 X frágil síndrome @5 01`
C03	`02`	`X`	`FRE`	`@0 Tremblement @5 04`
C03	`02`	`X`	`ENG`	`@0 Tremor @5 04`
C03	`02`	`X`	`SPA`	`@0 Temblor @5 04`
C03	`03`	`X`	`FRE`	`@0 Ataxie @5 07`
C03	`03`	`X`	`ENG`	`@0 Ataxia @5 07`
C03	`03`	`X`	`SPA`	`@0 Ataxia @5 07`
C03	`04`	`X`	`FRE`	`@0 Phénotype @5 10`
C03	`04`	`X`	`ENG`	`@0 Phenotype @5 10`
C03	`04`	`X`	`SPA`	`@0 Fenotipo @5 10`
C03	`05`	`X`	`FRE`	`@0 Etude cas @5 17`
C03	`05`	`X`	`ENG`	`@0 Case study @5 17`
C03	`05`	`X`	`SPA`	`@0 Estudio caso @5 17`
C03	`06`	`X`	`FRE`	`@0 Diagnostic @5 18`
C03	`06`	`X`	`ENG`	`@0 Diagnosis @5 18`
C03	`06`	`X`	`SPA`	`@0 Diagnóstico @5 18`
C03	`07`	`X`	`FRE`	`@0 Déterminisme génétique @5 19`
C03	`07`	`X`	`ENG`	`@0 Genetic determinism @5 19`
C03	`07`	`X`	`SPA`	`@0 Determinismo genético @5 19`
C03	`08`	`X`	`FRE`	`@0 Personne âgée @5 20`
C03	`08`	`X`	`ENG`	`@0 Elderly @5 20`
C03	`08`	`X`	`SPA`	`@0 Anciano @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 Prémutation @4 CD @5 96`
C03	`10`	`X`	`ENG`	`@0 Premutation @4 CD @5 96`
C07	`01`	`X`	`FRE`	`@0 Homme`
C07	`01`	`X`	`ENG`	`@0 Human`
C07	`01`	`X`	`SPA`	`@0 Hombre`
C07	`02`	`X`	`FRE`	`@0 Fragilité chromosomique @5 37`
C07	`02`	`X`	`ENG`	`@0 Chromosome fragility @5 37`
C07	`02`	`X`	`SPA`	`@0 Fragilidad cromosómica @5 37`
C07	`03`	`X`	`FRE`	`@0 Maladie héréditaire @5 38`
C07	`03`	`X`	`ENG`	`@0 Genetic disease @5 38`
C07	`03`	`X`	`SPA`	`@0 Enfermedad hereditaria @5 38`
C07	`04`	`X`	`FRE`	`@0 Système nerveux pathologie @5 45`
C07	`04`	`X`	`ENG`	`@0 Nervous system diseases @5 45`
C07	`04`	`X`	`SPA`	`@0 Sistema nervioso patología @5 45`
C07	`05`	`X`	`FRE`	`@0 Trouble neurologique @5 46`
C07	`05`	`X`	`ENG`	`@0 Neurological disorder @5 46`
C07	`05`	`X`	`SPA`	`@0 Trastorno neurológico @5 46`
C07	`06`	`X`	`FRE`	`@0 Mouvement involontaire @5 47`
C07	`06`	`X`	`ENG`	`@0 Involuntary movement @5 47`
C07	`06`	`X`	`SPA`	`@0 Movimiento involuntario @5 47`
C07	`07`	`X`	`FRE`	`@0 Encéphale pathologie @5 53`
C07	`07`	`X`	`ENG`	`@0 Cerebral disorder @5 53`
C07	`07`	`X`	`SPA`	`@0 Encéfalo patología @5 53`
C07	`08`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 54`
C07	`08`	`X`	`ENG`	`@0 Central nervous system disease @5 54`
C07	`08`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 54`
N21				`@1 266`
N82				`@1 PSI`

Format Inist (serveur)

NO :	PASCAL 02-0456862 INIST
ET :	Tremor/ataxia syndrome in fragile X carrier males
AU :	LEEHEY (Maureen A.); HAGERMAN (Randi J.); LANDAU (William M.); GRIGSBY (Jim); TASSONE (Flora); HAGERMAN (Paul J.)
AF :	Department of Neurology, University of Colorado Health Sciences Center/Denver, Colorado/Etats-Unis (1 aut.); M.I.N.D. Institute, University of California at Davis Medical Center/Sacramento, California/Etats-Unis (2 aut.); Department of Neurology, Washington University School of Medicine/Saint Louis, Missouri/Etats-Unis (3 aut.); Department of Medicine, University of Colorado Health Sciences Center/Denver, Colorado/Etats-Unis (4 aut.); Department of Biological Chemistry, University of California at Davis School of Medicine/Davis, California/Etats-Unis (5 aut., 6 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2002; Vol. 17; No. 4; Pp. 744-745; Bibl. 8 ref.
LA :	Anglais
CC :	002B23E
FD :	X fragile syndrome; Tremblement; Ataxie; Phénotype; Etude cas; Diagnostic; Déterminisme génétique; Personne âgée; Mâle; Prémutation
FG :	Homme; Fragilité chromosomique; Maladie héréditaire; Système nerveux pathologie; Trouble neurologique; Mouvement involontaire; Encéphale pathologie; Système nerveux central pathologie
ED :	Fragile X syndrome; Tremor; Ataxia; Phenotype; Case study; Diagnosis; Genetic determinism; Elderly; Male; Premutation
EG :	Human; Chromosome fragility; Genetic disease; Nervous system diseases; Neurological disorder; Involuntary movement; Cerebral disorder; Central nervous system disease
SD :	X frágil síndrome; Temblor; Ataxia; Fenotipo; Estudio caso; Diagnóstico; Determinismo genético; Anciano; Macho
LO :	INIST-20953.354000108922560170
ID :	02-0456862

Links to Exploration step

Pascal:02-0456862

Le document en format XML

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<s5>96</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Premutation</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Homme</s0>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Human</s0>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Hombre</s0>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Fragilité chromosomique</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Chromosome fragility</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Fragilidad cromosómica</s0>
<s5>37</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>38</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>45</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>45</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>45</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>46</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>46</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>46</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Mouvement involontaire</s0>
<s5>47</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Involuntary movement</s0>
<s5>47</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Movimiento involuntario</s0>
<s5>47</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>53</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>53</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>53</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>54</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>54</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>54</s5>
</fC07>
<fN21><s1>266</s1>
</fN21>
<fN82><s1>PSI</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 02-0456862 INIST</NO>
<ET>Tremor/ataxia syndrome in fragile X carrier males</ET>
<AU>LEEHEY (Maureen A.); HAGERMAN (Randi J.); LANDAU (William M.); GRIGSBY (Jim); TASSONE (Flora); HAGERMAN (Paul J.)</AU>
<AF>Department of Neurology, University of Colorado Health Sciences Center/Denver, Colorado/Etats-Unis (1 aut.); M.I.N.D. Institute, University of California at Davis Medical Center/Sacramento, California/Etats-Unis (2 aut.); Department of Neurology, Washington University School of Medicine/Saint Louis, Missouri/Etats-Unis (3 aut.); Department of Medicine, University of Colorado Health Sciences Center/Denver, Colorado/Etats-Unis (4 aut.); Department of Biological Chemistry, University of California at Davis School of Medicine/Davis, California/Etats-Unis (5 aut., 6 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2002; Vol. 17; No. 4; Pp. 744-745; Bibl. 8 ref.</SO>
<LA>Anglais</LA>
<CC>002B23E</CC>
<FD>X fragile syndrome; Tremblement; Ataxie; Phénotype; Etude cas; Diagnostic; Déterminisme génétique; Personne âgée; Mâle; Prémutation</FD>
<FG>Homme; Fragilité chromosomique; Maladie héréditaire; Système nerveux pathologie; Trouble neurologique; Mouvement involontaire; Encéphale pathologie; Système nerveux central pathologie</FG>
<ED>Fragile X syndrome; Tremor; Ataxia; Phenotype; Case study; Diagnosis; Genetic determinism; Elderly; Male; Premutation</ED>
<EG>Human; Chromosome fragility; Genetic disease; Nervous system diseases; Neurological disorder; Involuntary movement; Cerebral disorder; Central nervous system disease</EG>
<SD>X frágil síndrome; Temblor; Ataxia; Fenotipo; Estudio caso; Diagnóstico; Determinismo genético; Anciano; Macho</SD>
<LO>INIST-20953.354000108922560170</LO>
<ID>02-0456862</ID>
</server>
</inist>
</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Tremor/ataxia syndrome in fragile X carrier males

Tremor/ataxia syndrome in fragile X carrier males

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