Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration
Identifieur interne : 006012 ( Main/Curation ); précédent : 006011; suivant : 006013Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration
Auteurs : Nir Giladi [États-Unis] ; Stanley Fahn [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 1992.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Atrophy, Basal Ganglia (pathology), Basal Ganglia Diseases (diagnosis), Basal Ganglia Diseases (pathology), Basal ganglion, Brain (vertebrata), Cerebral Cortex (pathology), Degeneration, Diagnosis, Diagnosis, Differential, Functional Laterality (physiology), Hemiatrophy, Human, Humans, Magnetic Resonance Imaging, Male, Muscular Atrophy (diagnosis), Muscular Atrophy (pathology), Nerve Degeneration (physiology), Neurologic Examination, Parkinson Disease, Secondary (diagnosis), Parkinson Disease, Secondary (pathology).
- MESH :
- diagnosis : Basal Ganglia Diseases, Muscular Atrophy, Parkinson Disease, Secondary.
- pathology : Basal Ganglia, Basal Ganglia Diseases, Cerebral Cortex, Muscular Atrophy, Parkinson Disease, Secondary.
- physiology : Functional Laterality, Nerve Degeneration.
- Adult, Atrophy, Diagnosis, Differential, Humans, Magnetic Resonance Imaging, Male, Neurologic Examination.
Url:
DOI: 10.1002/mds.870070419
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: Pour aller vers cette notice dans l'étape Curation :003D70
- to stream Istex, to step Curation: Pour aller vers cette notice dans l'étape Curation :003D70
- to stream Istex, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :004205
- to stream PubMed, to step Corpus: Pour aller vers cette notice dans l'étape Curation :004D05
- to stream PubMed, to step Curation: Pour aller vers cette notice dans l'étape Curation :004D05
- to stream PubMed, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :004D45
- to stream Ncbi, to step Merge: Pour aller vers cette notice dans l'étape Curation :000D18
- to stream Ncbi, to step Curation: Pour aller vers cette notice dans l'étape Curation :000D18
- to stream Ncbi, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :000D18
- to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :009295
- to stream PascalFrancis, to step Corpus: Pour aller vers cette notice dans l'étape Curation :003795
- to stream PascalFrancis, to step Curation: Pour aller vers cette notice dans l'étape Curation :003029
- to stream PascalFrancis, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :003809
- to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :009385
Links to Exploration step
ISTEX:3238DE35DE8AB3B23D0A1CC7BC333318B656F225Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration</title>
<author><name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
</author>
<author><name sortKey="Fahn, Stanley" sort="Fahn, Stanley" uniqKey="Fahn S" first="Stanley" last="Fahn">Stanley Fahn</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:3238DE35DE8AB3B23D0A1CC7BC333318B656F225</idno>
<date when="1992" year="1992">1992</date>
<idno type="doi">10.1002/mds.870070419</idno>
<idno type="url">https://api.istex.fr/document/3238DE35DE8AB3B23D0A1CC7BC333318B656F225/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003D70</idno>
<idno type="wicri:Area/Istex/Curation">003D70</idno>
<idno type="wicri:Area/Istex/Checkpoint">004205</idno>
<idno type="wicri:doubleKey">0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:1484539</idno>
<idno type="wicri:Area/PubMed/Corpus">004D05</idno>
<idno type="wicri:Area/PubMed/Curation">004D05</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004D45</idno>
<idno type="wicri:Area/Ncbi/Merge">000D18</idno>
<idno type="wicri:Area/Ncbi/Curation">000D18</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000D18</idno>
<idno type="wicri:doubleKey">0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome</idno>
<idno type="wicri:Area/Main/Merge">009295</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:93-0050919</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003795</idno>
<idno type="wicri:Area/PascalFrancis/Curation">003029</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">003809</idno>
<idno type="wicri:doubleKey">0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome</idno>
<idno type="wicri:Area/Main/Merge">009385</idno>
<idno type="wicri:Area/Main/Curation">006012</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration</title>
<author><name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<placeName><region type="state">État de New York</region>
</placeName>
<wicri:cityArea>Movement Disorder Group, Neurological Institute, Columbia‐Presbyterian Medical Center, New York</wicri:cityArea>
</affiliation>
</author>
<author><name sortKey="Fahn, Stanley" sort="Fahn, Stanley" uniqKey="Fahn S" first="Stanley" last="Fahn">Stanley Fahn</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<placeName><region type="state">État de New York</region>
</placeName>
<wicri:cityArea>Movement Disorder Group, Neurological Institute, Columbia‐Presbyterian Medical Center, New York</wicri:cityArea>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="1992">1992</date>
<biblScope unit="vol">7</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="384">384</biblScope>
<biblScope unit="page" to="385">385</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">3238DE35DE8AB3B23D0A1CC7BC333318B656F225</idno>
<idno type="DOI">10.1002/mds.870070419</idno>
<idno type="ArticleID">MDS870070419</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Basal Ganglia (pathology)</term>
<term>Basal Ganglia Diseases (diagnosis)</term>
<term>Basal Ganglia Diseases (pathology)</term>
<term>Basal ganglion</term>
<term>Brain (vertebrata)</term>
<term>Cerebral Cortex (pathology)</term>
<term>Degeneration</term>
<term>Diagnosis</term>
<term>Diagnosis, Differential</term>
<term>Functional Laterality (physiology)</term>
<term>Hemiatrophy</term>
<term>Human</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Muscular Atrophy (diagnosis)</term>
<term>Muscular Atrophy (pathology)</term>
<term>Nerve Degeneration (physiology)</term>
<term>Neurologic Examination</term>
<term>Parkinson Disease, Secondary (diagnosis)</term>
<term>Parkinson Disease, Secondary (pathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Basal Ganglia Diseases</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia</term>
<term>Basal Ganglia Diseases</term>
<term>Cerebral Cortex</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Functional Laterality</term>
<term>Nerve Degeneration</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Neurologic Examination</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Diagnostic</term>
<term>Dégénérescence</term>
<term>Encéphale</term>
<term>Homme</term>
<term>Hémiatrophie</term>
<term>Noyau gris central</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
</TEI>
<double idat="0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome"><INIST><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Hemiparkinsonism-hemiatrophy syndrome may mimic early-stage cortical-basal ganglionic degeneration</title>
<author><name sortKey="Giladi, N" sort="Giladi, N" uniqKey="Giladi N" first="N." last="Giladi">N. Giladi</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Columbia-presbyterian medical cent., neurological inst., movement disorder group</s1>
<s2>New York NY</s2>
<s3>USA</s3>
</inist:fA14>
<country>États-Unis</country>
<wicri:noRegion>New York NY</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S." last="Fahn">S. Fahn</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">93-0050919</idno>
<date when="1992">1992</date>
<idno type="stanalyst">PASCAL 93-0050919 INIST</idno>
<idno type="RBID">Pascal:93-0050919</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003795</idno>
<idno type="wicri:Area/PascalFrancis/Curation">003029</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">003809</idno>
<idno type="wicri:doubleKey">0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome</idno>
<idno type="wicri:Area/Main/Merge">009385</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Hemiparkinsonism-hemiatrophy syndrome may mimic early-stage cortical-basal ganglionic degeneration</title>
<author><name sortKey="Giladi, N" sort="Giladi, N" uniqKey="Giladi N" first="N." last="Giladi">N. Giladi</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Columbia-presbyterian medical cent., neurological inst., movement disorder group</s1>
<s2>New York NY</s2>
<s3>USA</s3>
</inist:fA14>
<country>États-Unis</country>
<wicri:noRegion>New York NY</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S." last="Fahn">S. Fahn</name>
</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="1992">1992</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>Brain (vertebrata)</term>
<term>Degeneration</term>
<term>Diagnosis</term>
<term>Hemiatrophy</term>
<term>Human</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dégénérescence</term>
<term>Encéphale</term>
<term>Diagnostic</term>
<term>Homme</term>
<term>Hémiatrophie</term>
<term>Noyau gris central</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
</INIST>
<ISTEX><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration</title>
<author><name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
</author>
<author><name sortKey="Fahn, Stanley" sort="Fahn, Stanley" uniqKey="Fahn S" first="Stanley" last="Fahn">Stanley Fahn</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:3238DE35DE8AB3B23D0A1CC7BC333318B656F225</idno>
<date when="1992" year="1992">1992</date>
<idno type="doi">10.1002/mds.870070419</idno>
<idno type="url">https://api.istex.fr/document/3238DE35DE8AB3B23D0A1CC7BC333318B656F225/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003D70</idno>
<idno type="wicri:Area/Istex/Curation">003D70</idno>
<idno type="wicri:Area/Istex/Checkpoint">004205</idno>
<idno type="wicri:doubleKey">0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:1484539</idno>
<idno type="wicri:Area/PubMed/Corpus">004D05</idno>
<idno type="wicri:Area/PubMed/Curation">004D05</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004D45</idno>
<idno type="wicri:Area/Ncbi/Merge">000D18</idno>
<idno type="wicri:Area/Ncbi/Curation">000D18</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000D18</idno>
<idno type="wicri:doubleKey">0885-3185:1992:Giladi N:hemiparkinsonism:hemiatrophy:syndrome</idno>
<idno type="wicri:Area/Main/Merge">009295</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration</title>
<author><name sortKey="Giladi, Nir" sort="Giladi, Nir" uniqKey="Giladi N" first="Nir" last="Giladi">Nir Giladi</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<placeName><region type="state">État de New York</region>
</placeName>
<wicri:cityArea>Movement Disorder Group, Neurological Institute, Columbia‐Presbyterian Medical Center, New York</wicri:cityArea>
</affiliation>
</author>
<author><name sortKey="Fahn, Stanley" sort="Fahn, Stanley" uniqKey="Fahn S" first="Stanley" last="Fahn">Stanley Fahn</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<placeName><region type="state">État de New York</region>
</placeName>
<wicri:cityArea>Movement Disorder Group, Neurological Institute, Columbia‐Presbyterian Medical Center, New York</wicri:cityArea>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="1992">1992</date>
<biblScope unit="vol">7</biblScope>
<biblScope unit="issue">4</biblScope>
<biblScope unit="page" from="384">384</biblScope>
<biblScope unit="page" to="385">385</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">3238DE35DE8AB3B23D0A1CC7BC333318B656F225</idno>
<idno type="DOI">10.1002/mds.870070419</idno>
<idno type="ArticleID">MDS870070419</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Basal Ganglia (pathology)</term>
<term>Basal Ganglia Diseases (diagnosis)</term>
<term>Basal Ganglia Diseases (pathology)</term>
<term>Cerebral Cortex (pathology)</term>
<term>Diagnosis, Differential</term>
<term>Functional Laterality (physiology)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Muscular Atrophy (diagnosis)</term>
<term>Muscular Atrophy (pathology)</term>
<term>Nerve Degeneration (physiology)</term>
<term>Neurologic Examination</term>
<term>Parkinson Disease, Secondary (diagnosis)</term>
<term>Parkinson Disease, Secondary (pathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Basal Ganglia Diseases</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia</term>
<term>Basal Ganglia Diseases</term>
<term>Cerebral Cortex</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Functional Laterality</term>
<term>Nerve Degeneration</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Neurologic Examination</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
</TEI>
</ISTEX>
</double>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 006012 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 006012 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Curation |type= RBID |clé= ISTEX:3238DE35DE8AB3B23D0A1CC7BC333318B656F225 |texte= Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration }}
This area was generated with Dilib version V0.6.23. |