MovDisordV3, PascalFrancis, Corpus, bibRecord, 000989

Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review

Identifieur interne : 000989 ( PascalFrancis/Corpus ); précédent : 000988; suivant : 000990

Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review

Auteurs : Araceli Alonso-Canovas ; Petra Katschnig ; Arianna Tucci ; Miryam Carecchio ; Nicholas W. Wood ; Mark Edwards ; Juan Carlos Martinez Castrillo ; Derek Burke ; Simon Heales ; Kailash P. Bhatia

Source :

Movement disorders [ 0885-3185 ] ; 2010.

RBID : Pascal:10-0377349

Descripteurs français

Pascal (Inist)
- Parkinsonisme, Apraxie, Sphingolipidose héréditaire de Gaucher, Pathologie du système nerveux, Regard, Etude cas, Lipide.

English descriptors

KwdEn :
- Apraxia, Case study, Gaucher disease, Gaze, Lipids, Nervous system diseases, Parkinsonism.

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 25`
A06				`@2 10`
A08	`01`	`1`	`ENG`	`@1 Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review`
A11	`01`	`1`		`@1 ALONSO-CANOVAS (Araceli)`
A11	`02`	`1`		`@1 KATSCHNIG (Petra)`
A11	`03`	`1`		`@1 TUCCI (Arianna)`
A11	`04`	`1`		`@1 CARECCHIO (Miryam)`
A11	`05`	`1`		`@1 WOOD (Nicholas W.)`
A11	`06`	`1`		`@1 EDWARDS (Mark)`
A11	`07`	`1`		`@1 MARTINEZ CASTRILLO (Juan Carlos)`
A11	`08`	`1`		`@1 BURKE (Derek)`
A11	`09`	`1`		`@1 HEALES (Simon)`
A11	`10`	`1`		`@1 BHATIA (Kailash P.)`
A14	`01`			`@1 Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London @2 London @3 GBR @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 10 aut.`
A14	`02`			`@1 Department of Neurology Hospital Universitario Ramon y Cajal @2 Madrid @3 ESP @Z 1 aut. @Z 7 aut.`
A14	`03`			`@1 Department of Molecular Neuroscience Institute of Neurology University College London @2 London @3 GBR @Z 3 aut. @Z 9 aut.`
A14	`04`			`@1 Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital @2 London @3 GBR @Z 8 aut. @Z 9 aut.`
A14	`05`			`@1 Neurometabolic Unit National Hospital for Neurology and Neurosurgery Queen Square @2 London @3 GBR @Z 9 aut.`
A20				`@1 1506-1509`
A21				`@1 2010`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000194762830290`
A44				`@0 0000 @1 © 2010 INIST-CNRS. All rights reserved.`
A45				`@0 10 ref.`
A47	`01`	`1`		`@0 10-0377349`
A60				`@1 P @3 LT`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C02	`01`	`X`		`@0 002B17`
C02	`02`	`X`		`@0 002B17G`
C03	`01`	`X`	`FRE`	`@0 Parkinsonisme @2 NM @5 01`
C03	`01`	`X`	`ENG`	`@0 Parkinsonism @2 NM @5 01`
C03	`01`	`X`	`SPA`	`@0 Parkinson síndrome @2 NM @5 01`
C03	`02`	`X`	`FRE`	`@0 Apraxie @5 02`
C03	`02`	`X`	`ENG`	`@0 Apraxia @5 02`
C03	`02`	`X`	`SPA`	`@0 Apraxia @5 02`
C03	`03`	`X`	`FRE`	`@0 Sphingolipidose héréditaire de Gaucher @5 03`
C03	`03`	`X`	`ENG`	`@0 Gaucher disease @5 03`
C03	`03`	`X`	`SPA`	`@0 Esfingolipidosis hereditaria Gaucher @5 03`
C03	`04`	`X`	`FRE`	`@0 Pathologie du système nerveux @5 04`
C03	`04`	`X`	`ENG`	`@0 Nervous system diseases @5 04`
C03	`04`	`X`	`SPA`	`@0 Sistema nervioso patología @5 04`
C03	`05`	`X`	`FRE`	`@0 Regard @5 09`
C03	`05`	`X`	`ENG`	`@0 Gaze @5 09`
C03	`05`	`X`	`SPA`	`@0 Mirada @5 09`
C03	`06`	`X`	`FRE`	`@0 Etude cas @5 10`
C03	`06`	`X`	`ENG`	`@0 Case study @5 10`
C03	`06`	`X`	`SPA`	`@0 Estudio caso @5 10`
C03	`07`	`X`	`FRE`	`@0 Lipide @5 78`
C03	`07`	`X`	`ENG`	`@0 Lipids @5 78`
C03	`07`	`X`	`SPA`	`@0 Lípido @5 78`
C07	`01`	`X`	`FRE`	`@0 Pathologie de l'encéphale @5 38`
C07	`01`	`X`	`ENG`	`@0 Cerebral disorder @5 38`
C07	`01`	`X`	`SPA`	`@0 Encéfalo patología @5 38`
C07	`02`	`X`	`FRE`	`@0 Pathologie du système nerveux central @5 39`
C07	`02`	`X`	`ENG`	`@0 Central nervous system disease @5 39`
C07	`02`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 39`
C07	`03`	`X`	`FRE`	`@0 Trouble neurologique @5 40`
C07	`03`	`X`	`ENG`	`@0 Neurological disorder @5 40`
C07	`03`	`X`	`SPA`	`@0 Trastorno neurológico @5 40`
C07	`04`	`X`	`FRE`	`@0 Enzymopathie @5 41`
C07	`04`	`X`	`ENG`	`@0 Enzymopathy @5 41`
C07	`04`	`X`	`SPA`	`@0 Enzimopatía @5 41`
C07	`05`	`X`	`FRE`	`@0 Lipoïdose @5 42`
C07	`05`	`X`	`ENG`	`@0 Lipoidosis @5 42`
C07	`05`	`X`	`SPA`	`@0 Lipoidosis @5 42`
C07	`06`	`X`	`FRE`	`@0 Maladie héréditaire @5 43`
C07	`06`	`X`	`ENG`	`@0 Genetic disease @5 43`
C07	`06`	`X`	`SPA`	`@0 Enfermedad hereditaria @5 43`
C07	`07`	`X`	`FRE`	`@0 Maladie métabolique @5 44`
C07	`07`	`X`	`ENG`	`@0 Metabolic diseases @5 44`
C07	`07`	`X`	`SPA`	`@0 Metabolismo patología @5 44`
N21				`@1 242`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 10-0377349 INIST
ET :	Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review
AU :	ALONSO-CANOVAS (Araceli); KATSCHNIG (Petra); TUCCI (Arianna); CARECCHIO (Miryam); WOOD (Nicholas W.); EDWARDS (Mark); MARTINEZ CASTRILLO (Juan Carlos); BURKE (Derek); HEALES (Simon); BHATIA (Kailash P.)
AF :	Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London/London/Royaume-Uni (1 aut., 2 aut., 4 aut., 5 aut., 6 aut., 10 aut.); Department of Neurology Hospital Universitario Ramon y Cajal/Madrid/Espagne (1 aut., 7 aut.); Department of Molecular Neuroscience Institute of Neurology University College London/London/Royaume-Uni (3 aut., 9 aut.); Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital/London/Royaume-Uni (8 aut., 9 aut.); Neurometabolic Unit National Hospital for Neurology and Neurosurgery Queen Square/London/Royaume-Uni (9 aut.)
DT :	Publication en série; Lettre à l'éditeur; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2010; Vol. 25; No. 10; Pp. 1506-1509; Bibl. 10 ref.
LA :	Anglais
CC :	002B17; 002B17G
FD :	Parkinsonisme; Apraxie; Sphingolipidose héréditaire de Gaucher; Pathologie du système nerveux; Regard; Etude cas; Lipide
FG :	Pathologie de l'encéphale; Pathologie du système nerveux central; Trouble neurologique; Enzymopathie; Lipoïdose; Maladie héréditaire; Maladie métabolique
ED :	Parkinsonism; Apraxia; Gaucher disease; Nervous system diseases; Gaze; Case study; Lipids
EG :	Cerebral disorder; Central nervous system disease; Neurological disorder; Enzymopathy; Lipoidosis; Genetic disease; Metabolic diseases
SD :	Parkinson síndrome; Apraxia; Esfingolipidosis hereditaria Gaucher; Sistema nervioso patología; Mirada; Estudio caso; Lípido
LO :	INIST-20953.354000194762830290
ID :	10-0377349

Links to Exploration step

Pascal:10-0377349

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review</title>
<author><name sortKey="Alonso Canovas, Araceli" sort="Alonso Canovas, Araceli" uniqKey="Alonso Canovas A" first="Araceli" last="Alonso-Canovas">Araceli Alonso-Canovas</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurology Hospital Universitario Ramon y Cajal</s1>
<s2>Madrid</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Katschnig, Petra" sort="Katschnig, Petra" uniqKey="Katschnig P" first="Petra" last="Katschnig">Petra Katschnig</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Tucci, Arianna" sort="Tucci, Arianna" uniqKey="Tucci A" first="Arianna" last="Tucci">Arianna Tucci</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Molecular Neuroscience Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>3 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Carecchio, Miryam" sort="Carecchio, Miryam" uniqKey="Carecchio M" first="Miryam" last="Carecchio">Miryam Carecchio</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W." last="Wood">Nicholas W. Wood</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Edwards, Mark" sort="Edwards, Mark" uniqKey="Edwards M" first="Mark" last="Edwards">Mark Edwards</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Martinez Castrillo, Juan Carlos" sort="Martinez Castrillo, Juan Carlos" uniqKey="Martinez Castrillo J" first="Juan Carlos" last="Martinez Castrillo">Juan Carlos Martinez Castrillo</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurology Hospital Universitario Ramon y Cajal</s1>
<s2>Madrid</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Burke, Derek" sort="Burke, Derek" uniqKey="Burke D" first="Derek" last="Burke">Derek Burke</name>
<affiliation><inist:fA14 i1="04"><s1>Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Heales, Simon" sort="Heales, Simon" uniqKey="Heales S" first="Simon" last="Heales">Simon Heales</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Molecular Neuroscience Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>3 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="04"><s1>Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="05"><s1>Neurometabolic Unit National Hospital for Neurology and Neurosurgery Queen Square</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">10-0377349</idno>
<date when="2010">2010</date>
<idno type="stanalyst">PASCAL 10-0377349 INIST</idno>
<idno type="RBID">Pascal:10-0377349</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000989</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review</title>
<author><name sortKey="Alonso Canovas, Araceli" sort="Alonso Canovas, Araceli" uniqKey="Alonso Canovas A" first="Araceli" last="Alonso-Canovas">Araceli Alonso-Canovas</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurology Hospital Universitario Ramon y Cajal</s1>
<s2>Madrid</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Katschnig, Petra" sort="Katschnig, Petra" uniqKey="Katschnig P" first="Petra" last="Katschnig">Petra Katschnig</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Tucci, Arianna" sort="Tucci, Arianna" uniqKey="Tucci A" first="Arianna" last="Tucci">Arianna Tucci</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Molecular Neuroscience Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>3 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Carecchio, Miryam" sort="Carecchio, Miryam" uniqKey="Carecchio M" first="Miryam" last="Carecchio">Miryam Carecchio</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W." last="Wood">Nicholas W. Wood</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Edwards, Mark" sort="Edwards, Mark" uniqKey="Edwards M" first="Mark" last="Edwards">Mark Edwards</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Martinez Castrillo, Juan Carlos" sort="Martinez Castrillo, Juan Carlos" uniqKey="Martinez Castrillo J" first="Juan Carlos" last="Martinez Castrillo">Juan Carlos Martinez Castrillo</name>
<affiliation><inist:fA14 i1="02"><s1>Department of Neurology Hospital Universitario Ramon y Cajal</s1>
<s2>Madrid</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Burke, Derek" sort="Burke, Derek" uniqKey="Burke D" first="Derek" last="Burke">Derek Burke</name>
<affiliation><inist:fA14 i1="04"><s1>Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Heales, Simon" sort="Heales, Simon" uniqKey="Heales S" first="Simon" last="Heales">Simon Heales</name>
<affiliation><inist:fA14 i1="03"><s1>Department of Molecular Neuroscience Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>3 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="04"><s1>Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation><inist:fA14 i1="05"><s1>Neurometabolic Unit National Hospital for Neurology and Neurosurgery Queen Square</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
<affiliation><inist:fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 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="2010">2010</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>Apraxia</term>
<term>Case study</term>
<term>Gaucher disease</term>
<term>Gaze</term>
<term>Lipids</term>
<term>Nervous system diseases</term>
<term>Parkinsonism</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Parkinsonisme</term>
<term>Apraxie</term>
<term>Sphingolipidose héréditaire de Gaucher</term>
<term>Pathologie du   système nerveux</term>
<term>Regard</term>
<term>Etude cas</term>
<term>Lipide</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</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>25</s2>
</fA05>
<fA06><s2>10</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>ALONSO-CANOVAS (Araceli)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>KATSCHNIG (Petra)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>TUCCI (Arianna)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>CARECCHIO (Miryam)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>WOOD (Nicholas W.)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>EDWARDS (Mark)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>MARTINEZ CASTRILLO (Juan Carlos)</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>BURKE (Derek)</s1>
</fA11>
<fA11 i1="09" i2="1"><s1>HEALES (Simon)</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>BHATIA (Kailash P.)</s1>
</fA11>
<fA14 i1="01"><s1>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Department of Neurology Hospital Universitario Ramon y Cajal</s1>
<s2>Madrid</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Department of Molecular Neuroscience Institute of Neurology University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>3 aut.</sZ>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="05"><s1>Neurometabolic Unit National Hospital for Neurology and Neurosurgery Queen Square</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA20><s1>1506-1509</s1>
</fA20>
<fA21><s1>2010</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>20953</s2>
<s5>354000194762830290</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2010 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>10 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>10-0377349</s0>
</fA47>
<fA60><s1>P</s1>
<s3>LT</s3>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Movement disorders</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<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>Parkinsonisme</s0>
<s2>NM</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Parkinsonism</s0>
<s2>NM</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Parkinson síndrome</s0>
<s2>NM</s2>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Apraxie</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Apraxia</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Apraxia</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Sphingolipidose héréditaire de Gaucher</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Gaucher disease</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Esfingolipidosis hereditaria Gaucher</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>Regard</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Gaze</s0>
<s5>09</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Mirada</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Etude cas</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Case study</s0>
<s5>10</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Estudio caso</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Lipide</s0>
<s5>78</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Lipids</s0>
<s5>78</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Lípido</s0>
<s5>78</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'encéphale</s0>
<s5>38</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>38</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Pathologie du   système nerveux central</s0>
<s5>39</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Trouble neurologique</s0>
<s5>40</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Neurological disorder</s0>
<s5>40</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Trastorno neurológico</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Enzymopathie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Enzymopathy</s0>
<s5>41</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Enzimopatía</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Lipoïdose</s0>
<s5>42</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Lipoidosis</s0>
<s5>42</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Lipoidosis</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Maladie héréditaire</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Genetic disease</s0>
<s5>43</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Enfermedad hereditaria</s0>
<s5>43</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE"><s0>Maladie métabolique</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG"><s0>Metabolic diseases</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA"><s0>Metabolismo patología</s0>
<s5>44</s5>
</fC07>
<fN21><s1>242</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 10-0377349 INIST</NO>
<ET>Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review</ET>
<AU>ALONSO-CANOVAS (Araceli); KATSCHNIG (Petra); TUCCI (Arianna); CARECCHIO (Miryam); WOOD (Nicholas W.); EDWARDS (Mark); MARTINEZ CASTRILLO (Juan Carlos); BURKE (Derek); HEALES (Simon); BHATIA (Kailash P.)</AU>
<AF>Sobell Department of Motor Neuroscience and Movement Disorders Institute of Neurology University College London/London/Royaume-Uni (1 aut., 2 aut., 4 aut., 5 aut., 6 aut., 10 aut.); Department of Neurology Hospital Universitario Ramon y Cajal/Madrid/Espagne (1 aut., 7 aut.); Department of Molecular Neuroscience Institute of Neurology University College London/London/Royaume-Uni (3 aut., 9 aut.); Enzyme Unit Department of Chemical Pathology Great Ormond Street Hospital/London/Royaume-Uni (8 aut., 9 aut.); Neurometabolic Unit National Hospital for Neurology and Neurosurgery Queen Square/London/Royaume-Uni (9 aut.)</AF>
<DT>Publication en série; Lettre à l'éditeur; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2010; Vol. 25; No. 10; Pp. 1506-1509; Bibl. 10 ref.</SO>
<LA>Anglais</LA>
<CC>002B17; 002B17G</CC>
<FD>Parkinsonisme; Apraxie; Sphingolipidose héréditaire de Gaucher; Pathologie du   système nerveux; Regard; Etude cas; Lipide</FD>
<FG>Pathologie de l'encéphale; Pathologie du   système nerveux central; Trouble neurologique; Enzymopathie; Lipoïdose; Maladie héréditaire; Maladie métabolique</FG>
<ED>Parkinsonism; Apraxia; Gaucher disease; Nervous system diseases; Gaze; Case study; Lipids</ED>
<EG>Cerebral disorder; Central nervous system disease; Neurological disorder; Enzymopathy; Lipoidosis; Genetic disease; Metabolic diseases</EG>
<SD>Parkinson síndrome; Apraxia; Esfingolipidosis hereditaria Gaucher; Sistema nervioso patología; Mirada; Estudio caso; Lípido</SD>
<LO>INIST-20953.354000194762830290</LO>
<ID>10-0377349</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 000989 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 000989 | 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:10-0377349
   |texte=   Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review
}}

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)

Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review

Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review

Source :

Descripteurs français

English descriptors

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