MovDisordV3, PascalFrancis, Corpus, bibRecord, 001F70

Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation

Identifieur interne : 001F70 ( PascalFrancis/Corpus ); précédent : 001F69; suivant : 001F71

Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation

Auteurs : Angela Deutschl Nder ; Friedrich Asmus ; Thomas Gasser ; Ulrich Steude ; Kai Bötzel

Source :

Movement disorders [ 0885-3185 ] ; 2005.

RBID : Pascal:05-0149713

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Sporadique, Dystonie, Parkinsonisme, Contrôle moteur.

English descriptors

KwdEn :
- Dystonia, Motor control, Nervous system diseases, Parkinsonism, Sporadic.

Abstract

We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0885-3185`
A03		`1`		`@0 Mov. disord.`
A05				`@2 20`
A06				`@2 2`
A08	`01`	`1`	`ENG`	`@1 Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation`
A11	`01`	`1`		`@1 DEUTSCHLÄNDER (Angela)`
A11	`02`	`1`		`@1 ASMUS (Friedrich)`
A11	`03`	`1`		`@1 GASSER (Thomas)`
A11	`04`	`1`		`@1 STEUDE (Ulrich)`
A11	`05`	`1`		`@1 BÖTZEL (Kai)`
A14	`01`			`@1 Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University @2 Munich @3 DEU @Z 1 aut. @Z 5 aut.`
A14	`02`			`@1 Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen @2 Tubingen @3 DEU @Z 2 aut. @Z 3 aut.`
A14	`03`			`@1 Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians University @2 Munich @3 DEU @Z 4 aut.`
A20				`@1 254-257`
A21				`@1 2005`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000126378730230`
A44				`@0 0000 @1 © 2005 INIST-CNRS. All rights reserved.`
A45				`@0 21 ref.`
A47	`01`	`1`		`@0 05-0149713`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	`@0 We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms.`
C02	`01`	`X`		`@0 002B17`
C02	`02`	`X`		`@0 002B17H`
C02	`03`	`X`		`@0 002B17G`
C03	`01`	`X`	`FRE`	`@0 Système nerveux pathologie @5 01`
C03	`01`	`X`	`ENG`	`@0 Nervous system diseases @5 01`
C03	`01`	`X`	`SPA`	`@0 Sistema nervioso patología @5 01`
C03	`02`	`X`	`FRE`	`@0 Sporadique @5 02`
C03	`02`	`X`	`ENG`	`@0 Sporadic @5 02`
C03	`02`	`X`	`SPA`	`@0 Esporádico @5 02`
C03	`03`	`X`	`FRE`	`@0 Dystonie @5 04`
C03	`03`	`X`	`ENG`	`@0 Dystonia @5 04`
C03	`03`	`X`	`SPA`	`@0 Distonía @5 04`
C03	`04`	`X`	`FRE`	`@0 Parkinsonisme @2 NM @5 07`
C03	`04`	`X`	`ENG`	`@0 Parkinsonism @2 NM @5 07`
C03	`04`	`X`	`SPA`	`@0 Parkinson síndrome @2 NM @5 07`
C03	`05`	`X`	`FRE`	`@0 Contrôle moteur @5 25`
C03	`05`	`X`	`ENG`	`@0 Motor control @5 25`
C03	`05`	`X`	`SPA`	`@0 Control motor @5 25`
C07	`01`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 37`
C07	`01`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 37`
C07	`01`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 37`
C07	`02`	`X`	`FRE`	`@0 Mouvement involontaire @5 38`
C07	`02`	`X`	`ENG`	`@0 Involuntary movement @5 38`
C07	`02`	`X`	`SPA`	`@0 Movimiento involuntario @5 38`
C07	`03`	`X`	`FRE`	`@0 Muscle strié pathologie @5 39`
C07	`03`	`X`	`ENG`	`@0 Striated muscle disease @5 39`
C07	`03`	`X`	`SPA`	`@0 Músculo estriado patología @5 39`
C07	`04`	`X`	`FRE`	`@0 Trouble neurologique @5 40`
C07	`04`	`X`	`ENG`	`@0 Neurological disorder @5 40`
C07	`04`	`X`	`SPA`	`@0 Trastorno neurológico @5 40`
C07	`05`	`X`	`FRE`	`@0 Encéphale pathologie @5 41`
C07	`05`	`X`	`ENG`	`@0 Cerebral disorder @5 41`
C07	`05`	`X`	`SPA`	`@0 Encéfalo patología @5 41`
C07	`06`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 42`
C07	`06`	`X`	`ENG`	`@0 Central nervous system disease @5 42`
C07	`06`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 42`
N21				`@1 101`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 05-0149713 INIST
ET :	Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation
AU :	DEUTSCHLÄNDER (Angela); ASMUS (Friedrich); GASSER (Thomas); STEUDE (Ulrich); BÖTZEL (Kai)
AF :	Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University/Munich/Allemagne (1 aut., 5 aut.); Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen/Tubingen/Allemagne (2 aut., 3 aut.); Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians University/Munich/Allemagne (4 aut.)
DT :	Publication en série; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. 2; Pp. 254-257; Bibl. 21 ref.
LA :	Anglais
EA :	We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms.
CC :	002B17; 002B17H; 002B17G
FD :	Système nerveux pathologie; Sporadique; Dystonie; Parkinsonisme; Contrôle moteur
FG :	Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie
ED :	Nervous system diseases; Sporadic; Dystonia; Parkinsonism; Motor control
EG :	Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease
SD :	Sistema nervioso patología; Esporádico; Distonía; Parkinson síndrome; Control motor
LO :	INIST-20953.354000126378730230
ID :	05-0149713

Links to Exploration step

Pascal:05-0149713

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation</title>
<author><name sortKey="Deutschl Nder, Angela" sort="Deutschl Nder, Angela" uniqKey="Deutschl Nder A" first="Angela" last="Deutschl Nder">Angela Deutschl Nder</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Asmus, Friedrich" sort="Asmus, Friedrich" uniqKey="Asmus F" first="Friedrich" last="Asmus">Friedrich Asmus</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen</s1>
<s2>Tubingen</s2>
<s3>DEU</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Gasser, Thomas" sort="Gasser, Thomas" uniqKey="Gasser T" first="Thomas" last="Gasser">Thomas Gasser</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen</s1>
<s2>Tubingen</s2>
<s3>DEU</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Steude, Ulrich" sort="Steude, Ulrich" uniqKey="Steude U" first="Ulrich" last="Steude">Ulrich Steude</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Botzel, Kai" sort="Botzel, Kai" uniqKey="Botzel K" first="Kai" last="Bötzel">Kai Bötzel</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">05-0149713</idno>
<date when="2005">2005</date>
<idno type="stanalyst">PASCAL 05-0149713 INIST</idno>
<idno type="RBID">Pascal:05-0149713</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">001F70</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation</title>
<author><name sortKey="Deutschl Nder, Angela" sort="Deutschl Nder, Angela" uniqKey="Deutschl Nder A" first="Angela" last="Deutschl Nder">Angela Deutschl Nder</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Asmus, Friedrich" sort="Asmus, Friedrich" uniqKey="Asmus F" first="Friedrich" last="Asmus">Friedrich Asmus</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen</s1>
<s2>Tubingen</s2>
<s3>DEU</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Gasser, Thomas" sort="Gasser, Thomas" uniqKey="Gasser T" first="Thomas" last="Gasser">Thomas Gasser</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen</s1>
<s2>Tubingen</s2>
<s3>DEU</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Steude, Ulrich" sort="Steude, Ulrich" uniqKey="Steude U" first="Ulrich" last="Steude">Ulrich Steude</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Botzel, Kai" sort="Botzel, Kai" uniqKey="Botzel K" first="Kai" last="Bötzel">Kai Bötzel</name>
<affiliation><inist:fA14 i1="01"><s1>Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>5 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="2005">2005</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>Dystonia</term>
<term>Motor control</term>
<term>Nervous system diseases</term>
<term>Parkinsonism</term>
<term>Sporadic</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Sporadique</term>
<term>Dystonie</term>
<term>Parkinsonisme</term>
<term>Contrôle moteur</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms.</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>20</s2>
</fA05>
<fA06><s2>2</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>DEUTSCHLÄNDER (Angela)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>ASMUS (Friedrich)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>GASSER (Thomas)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>STEUDE (Ulrich)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>BÖTZEL (Kai)</s1>
</fA11>
<fA14 i1="01"><s1>Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen</s1>
<s2>Tubingen</s2>
<s3>DEU</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians University</s1>
<s2>Munich</s2>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA20><s1>254-257</s1>
</fA20>
<fA21><s1>2005</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>20953</s2>
<s5>354000126378730230</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2005 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>21 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>05-0149713</s0>
</fA47>
<fA60><s1>P</s1>
</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>We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B17</s0>
</fC02>
<fC02 i1="02" i2="X"><s0>002B17H</s0>
</fC02>
<fC02 i1="03" i2="X"><s0>002B17G</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Sporadique</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Sporadic</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Esporádico</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Dystonie</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Dystonia</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Distonía</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Parkinsonisme</s0>
<s2>NM</s2>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Parkinsonism</s0>
<s2>NM</s2>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Parkinson síndrome</s0>
<s2>NM</s2>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Contrôle moteur</s0>
<s5>25</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Motor control</s0>
<s5>25</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Control motor</s0>
<s5>25</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Mouvement involontaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Involuntary movement</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Movimiento involuntario</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Muscle strié pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Striated muscle disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Músculo estriado patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>42</s5>
</fC07>
<fN21><s1>101</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 05-0149713 INIST</NO>
<ET>Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation</ET>
<AU>DEUTSCHLÄNDER (Angela); ASMUS (Friedrich); GASSER (Thomas); STEUDE (Ulrich); BÖTZEL (Kai)</AU>
<AF>Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians University/Munich/Allemagne (1 aut., 5 aut.); Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen/Tubingen/Allemagne (2 aut., 3 aut.); Department of Neurosurgery, Klinikum Grosshadern, Ludwig-Maximilians University/Munich/Allemagne (4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. 2; Pp. 254-257; Bibl. 21 ref.</SO>
<LA>Anglais</LA>
<EA>We report on a woman who had a severe sporadic nonprogressive dystonia-parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid-onset dystonia-parkinsonism, except for autosomal-dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms.</EA>
<CC>002B17; 002B17H; 002B17G</CC>
<FD>Système nerveux pathologie; Sporadique; Dystonie; Parkinsonisme; Contrôle moteur</FD>
<FG>Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie</FG>
<ED>Nervous system diseases; Sporadic; Dystonia; Parkinsonism; Motor control</ED>
<EG>Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Esporádico; Distonía; Parkinson síndrome; Control motor</SD>
<LO>INIST-20953.354000126378730230</LO>
<ID>05-0149713</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 001F70 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 001F70 | 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:05-0149713
   |texte=   Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation
}}

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation

Sporadic rapid-onset dystonia-parkinsonism syndrome : Failure of bilateral pallidal stimulation

Source :

Descripteurs français

English descriptors

Abstract

Notice en format standard (ISO 2709)

Format Inist (serveur)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri