Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits
Identifieur interne : 000256 ( PascalFrancis/Corpus ); précédent : 000255; suivant : 000257Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits
Auteurs : Ralf Reilmann ; Silke Rumpf ; Heike Beckmann ; Raphael Koch ; Erich B. Ringelstein ; Herwig W. LangeSource :
- Movement disorders [ 0885-3185 ] ; 2012.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
|
---|
Format Inist (serveur)
NO : | PASCAL 12-0183678 INIST |
---|---|
ET : | Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits |
AU : | REILMANN (Ralf); RUMPF (Silke); BECKMANN (Heike); KOCH (Raphael); RINGELSTEIN (Erich B.); LANGE (Herwig W.) |
AF : | Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (1 aut., 2 aut., 3 aut., 5 aut., 6 aut.); Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (4 aut.) |
DT : | Publication en série; Courte communication, note brève; Niveau analytique |
SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2012; Vol. 27; No. 4; Pp. 555-559; Bibl. 19 ref. |
LA : | Anglais |
EA : | Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease. |
CC : | 002B17; 002B17G |
FD : | Chorée de Huntington; Trouble moteur; Déficit fonctionnel; Pathologie du système nerveux; Posture; Pronostic; Contrôle moteur; Noyau gris central |
FG : | Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Maladie héréditaire; Pathologie du système nerveux central; Trouble neurologique; Encéphale; Système nerveux central |
ED : | Huntington disease; Motor system disorder; Functional deficit; Nervous system diseases; Posture; Prognosis; Motor control; Basal ganglion |
EG : | Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease; Central nervous system disease; Neurological disorder; Encephalon; Central nervous system |
SD : | Corea Huntington; Trastorno motor; Deficiencia funcional; Sistema nervioso patología; Postura; Pronóstico; Control motor; Núcleo basal |
LO : | INIST-20953.354000194678450200 |
ID : | 12-0183678 |
Links to Exploration step
Pascal:12-0183678Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits</title>
<author><name sortKey="Reilmann, Ralf" sort="Reilmann, Ralf" uniqKey="Reilmann R" first="Ralf" last="Reilmann">Ralf Reilmann</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Rumpf, Silke" sort="Rumpf, Silke" uniqKey="Rumpf S" first="Silke" last="Rumpf">Silke Rumpf</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Beckmann, Heike" sort="Beckmann, Heike" uniqKey="Beckmann H" first="Heike" last="Beckmann">Heike Beckmann</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Koch, Raphael" sort="Koch, Raphael" uniqKey="Koch R" first="Raphael" last="Koch">Raphael Koch</name>
<affiliation><inist:fA14 i1="02"><s1>Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Ringelstein, Erich B" sort="Ringelstein, Erich B" uniqKey="Ringelstein E" first="Erich B." last="Ringelstein">Erich B. Ringelstein</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lange, Herwig W" sort="Lange, Herwig W" uniqKey="Lange H" first="Herwig W." last="Lange">Herwig W. Lange</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">12-0183678</idno>
<date when="2012">2012</date>
<idno type="stanalyst">PASCAL 12-0183678 INIST</idno>
<idno type="RBID">Pascal:12-0183678</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000256</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits</title>
<author><name sortKey="Reilmann, Ralf" sort="Reilmann, Ralf" uniqKey="Reilmann R" first="Ralf" last="Reilmann">Ralf Reilmann</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Rumpf, Silke" sort="Rumpf, Silke" uniqKey="Rumpf S" first="Silke" last="Rumpf">Silke Rumpf</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Beckmann, Heike" sort="Beckmann, Heike" uniqKey="Beckmann H" first="Heike" last="Beckmann">Heike Beckmann</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Koch, Raphael" sort="Koch, Raphael" uniqKey="Koch R" first="Raphael" last="Koch">Raphael Koch</name>
<affiliation><inist:fA14 i1="02"><s1>Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Ringelstein, Erich B" sort="Ringelstein, Erich B" uniqKey="Ringelstein E" first="Erich B." last="Ringelstein">Erich B. Ringelstein</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Lange, Herwig W" sort="Lange, Herwig W" uniqKey="Lange H" first="Herwig W." last="Lange">Herwig W. Lange</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Basal ganglion</term>
<term>Functional deficit</term>
<term>Huntington disease</term>
<term>Motor control</term>
<term>Motor system disorder</term>
<term>Nervous system diseases</term>
<term>Posture</term>
<term>Prognosis</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Chorée de Huntington</term>
<term>Trouble moteur</term>
<term>Déficit fonctionnel</term>
<term>Pathologie du système nerveux</term>
<term>Posture</term>
<term>Pronostic</term>
<term>Contrôle moteur</term>
<term>Noyau gris central</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.</div>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0885-3185</s0>
</fA01>
<fA03 i2="1"><s0>Mov. disord.</s0>
</fA03>
<fA05><s2>27</s2>
</fA05>
<fA06><s2>4</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>REILMANN (Ralf)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>RUMPF (Silke)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>BECKMANN (Heike)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>KOCH (Raphael)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>RINGELSTEIN (Erich B.)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>LANGE (Herwig W.)</s1>
</fA11>
<fA14 i1="01"><s1>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1</s1>
<s2>Muenster</s2>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA20><s1>555-559</s1>
</fA20>
<fA21><s1>2012</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>20953</s2>
<s5>354000194678450200</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2012 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>19 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>12-0183678</s0>
</fA47>
<fA60><s1>P</s1>
<s3>CC</s3>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Movement disorders</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B17</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B17G</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Chorée de Huntington</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Huntington disease</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Corea Huntington</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Trouble moteur</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Motor system disorder</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Trastorno motor</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Déficit fonctionnel</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Functional deficit</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Deficiencia funcional</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Pathologie du système nerveux</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Posture</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Posture</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Postura</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Pronostic</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Prognosis</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Pronóstico</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Contrôle moteur</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Motor control</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Control motor</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Noyau gris central</s0>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Basal ganglion</s0>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Núcleo basal</s0>
<s5>12</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'encéphale</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Syndrome extrapyramidal</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Pathologie du système nerveux central</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Encéphale</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Encephalon</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Encéfalo</s0>
<s5>44</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE"><s0>Système nerveux central</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG"><s0>Central nervous system</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Sistema nervioso central</s0>
<s5>45</s5>
</fC07>
<fN21><s1>142</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 12-0183678 INIST</NO>
<ET>Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits</ET>
<AU>REILMANN (Ralf); RUMPF (Silke); BECKMANN (Heike); KOCH (Raphael); RINGELSTEIN (Erich B.); LANGE (Herwig W.)</AU>
<AF>Department of Neurology, UKM, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (1 aut., 2 aut., 3 aut., 5 aut., 6 aut.); Institute of Biostatistics and Clinical Research, University of Muenster, Albert-Schweitzer-Campus 1/Muenster/Allemagne (4 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2012; Vol. 27; No. 4; Pp. 555-559; Bibl. 19 ref.</SO>
<LA>Anglais</LA>
<EA>Background: Postural deficits in Huntington's disease are linked to functional impairment. We investigated whether assessment of center-of-mass variability using posturography provides objective and quantitative measures that correlate to the severity of motor phenotype, functional measures, and genotype as assessed by a disease burden score (based on repeat length and age). In addition, we investigated whether withdrawing visual feedback facilitates the detection of postural deficits. Methods: Using a force plate, the ability of symptomatic Huntington's disease patients (n = 34) and controls (n = 20) to stand as stably as possible was assessed in eyes-open and eyes-closed conditions. Results: All posturographic measures (DISTANCE, VELOCITY, and SURFACE of centre-of-mass mobility) were increased in patients and correlated to (1) the UHDRS Total Motor Score, (2) the UHDRS Total Functional Capacity, (3) the UHDRS Functional Assessment Score, and (4) the disease burden score. Correlations to motor and functional measures were stronger when visual feedback was provided. Conclusions: Posturography may provide useful objective and quantitative measures of postural motor dysfunction in Huntington's disease.</EA>
<CC>002B17; 002B17G</CC>
<FD>Chorée de Huntington; Trouble moteur; Déficit fonctionnel; Pathologie du système nerveux; Posture; Pronostic; Contrôle moteur; Noyau gris central</FD>
<FG>Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Maladie héréditaire; Pathologie du système nerveux central; Trouble neurologique; Encéphale; Système nerveux central</FG>
<ED>Huntington disease; Motor system disorder; Functional deficit; Nervous system diseases; Posture; Prognosis; Motor control; Basal ganglion</ED>
<EG>Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Genetic disease; Central nervous system disease; Neurological disorder; Encephalon; Central nervous system</EG>
<SD>Corea Huntington; Trastorno motor; Deficiencia funcional; Sistema nervioso patología; Postura; Pronóstico; Control motor; Núcleo basal</SD>
<LO>INIST-20953.354000194678450200</LO>
<ID>12-0183678</ID>
</server>
</inist>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PascalFrancis/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000256 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 000256 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= PascalFrancis |étape= Corpus |type= RBID |clé= Pascal:12-0183678 |texte= Huntington's Disease: Objective Assessment of Posture-A Link Between Motor and Functional Deficits }}
This area was generated with Dilib version V0.6.23. |