Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review
Identifieur interne :
002330 ( PascalFrancis/Curation );
précédent :
002329;
suivant :
002331
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 [
Royaume-Uni,
Espagne] ;
Petra Katschnig [
Royaume-Uni] ;
Arianna Tucci [
Royaume-Uni] ;
Miryam Carecchio [
Royaume-Uni] ;
Nicholas W. Wood [
Royaume-Uni] ;
Mark Edwards [
Royaume-Uni] ;
Juan Carlos Martinez Castrillo [
Espagne] ;
Derek Burke [
Royaume-Uni] ;
Simon Heales [
Royaume-Uni] ;
Kailash P. Bhatia [
Royaume-Uni]
Source :
-
Movement disorders [ 0885-3185 ] ; 2010.
RBID : Pascal:10-0377349
Descripteurs français
English descriptors
pA |
A01 | 01 | 1 | | @0 0885-3185 |
---|
A03 | | 1 | | @0 Mov. disord. |
---|
A05 | | | | @2 25 |
---|
A06 | | | | @2 10 |
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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. |
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A47 | 01 | 1 | | @0 10-0377349 |
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A60 | | | | @1 P @3 LT |
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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 |
---|
|
Links toward previous steps (curation, corpus...)
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Pascal:10-0377349
Le document en format XML
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<term>Apraxie</term>
<term>Sphingolipidose héréditaire de Gaucher</term>
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<fA03 i2="1"><s0>Mov. disord.</s0>
</fA03>
<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>
<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>
</inist>
</record>
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