Apraxia in diseases of the basal ganglia.
Identifieur interne : 000294 ( Ncbi/Checkpoint ); précédent : 000293; suivant : 000295Apraxia in diseases of the basal ganglia.
Auteurs : E A RoySource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2000.
English descriptors
- KwdEn :
- Apraxia, Ideomotor (diagnosis), Apraxia, Ideomotor (physiopathology), Basal Ganglia (physiopathology), Basal Ganglia Diseases (diagnosis), Basal Ganglia Diseases (physiopathology), Brain Mapping, Humans, Multiple System Atrophy (diagnosis), Multiple System Atrophy (physiopathology), Parkinson Disease (diagnosis), Parkinson Disease (physiopathology), Supranuclear Palsy, Progressive (diagnosis), Supranuclear Palsy, Progressive (physiopathology).
- MESH :
- diagnosis : Apraxia, Ideomotor, Basal Ganglia Diseases, Multiple System Atrophy, Parkinson Disease, Supranuclear Palsy, Progressive.
- physiopathology : Apraxia, Ideomotor, Basal Ganglia, Basal Ganglia Diseases, Multiple System Atrophy, Parkinson Disease, Supranuclear Palsy, Progressive.
- Brain Mapping, Humans.
PubMed: 10928568
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 003F57
- to stream PubMed, to step Curation: 003F57
- to stream PubMed, to step Checkpoint: 004040
- to stream Ncbi, to step Merge: 000294
- to stream Ncbi, to step Curation: 000294
Links to Exploration step
pubmed:10928568Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Apraxia in diseases of the basal ganglia.</title>
<author><name sortKey="Roy, E A" sort="Roy, E A" uniqKey="Roy E" first="E A" last="Roy">E A Roy</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2000">2000</date>
<idno type="RBID">pubmed:10928568</idno>
<idno type="pmid">10928568</idno>
<idno type="wicri:Area/PubMed/Corpus">003F57</idno>
<idno type="wicri:Area/PubMed/Curation">003F57</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004040</idno>
<idno type="wicri:Area/Ncbi/Merge">000294</idno>
<idno type="wicri:Area/Ncbi/Curation">000294</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000294</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Apraxia in diseases of the basal ganglia.</title>
<author><name sortKey="Roy, E A" sort="Roy, E A" uniqKey="Roy E" first="E A" last="Roy">E A Roy</name>
</author>
</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2000" type="published">2000</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Apraxia, Ideomotor (diagnosis)</term>
<term>Apraxia, Ideomotor (physiopathology)</term>
<term>Basal Ganglia (physiopathology)</term>
<term>Basal Ganglia Diseases (diagnosis)</term>
<term>Basal Ganglia Diseases (physiopathology)</term>
<term>Brain Mapping</term>
<term>Humans</term>
<term>Multiple System Atrophy (diagnosis)</term>
<term>Multiple System Atrophy (physiopathology)</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (physiopathology)</term>
<term>Supranuclear Palsy, Progressive (diagnosis)</term>
<term>Supranuclear Palsy, Progressive (physiopathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Apraxia, Ideomotor</term>
<term>Basal Ganglia Diseases</term>
<term>Multiple System Atrophy</term>
<term>Parkinson Disease</term>
<term>Supranuclear Palsy, Progressive</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Apraxia, Ideomotor</term>
<term>Basal Ganglia</term>
<term>Basal Ganglia Diseases</term>
<term>Multiple System Atrophy</term>
<term>Parkinson Disease</term>
<term>Supranuclear Palsy, Progressive</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Brain Mapping</term>
<term>Humans</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list></list>
<tree><noCountry><name sortKey="Roy, E A" sort="Roy, E A" uniqKey="Roy E" first="E A" last="Roy">E A Roy</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Ncbi/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000294 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/biblio.hfd -nk 000294 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Ncbi |étape= Checkpoint |type= RBID |clé= pubmed:10928568 |texte= Apraxia in diseases of the basal ganglia. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/RBID.i -Sk "pubmed:10928568" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Checkpoint/biblio.hfd \ | NlmPubMed2Wicri -a MovDisordV3
This area was generated with Dilib version V0.6.23. |