Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".
Identifieur interne : 000625 ( Main/Exploration ); précédent : 000624; suivant : 000626Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".
Auteurs : Kishore R. Kumar [Australie] ; Christine KleinSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Arginine, Prions.
- genetics : Creutzfeldt-Jakob Syndrome, Mutation.
- physiopathology : Supranuclear Palsy, Progressive.
- Female, Humans.
DOI: 10.1002/mds.25089
PubMed: 22753322
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000D16
- to stream PubMed, to step Curation: 000D16
- to stream PubMed, to step Checkpoint: 000641
- to stream Ncbi, to step Merge: 003730
- to stream Ncbi, to step Curation: 003730
- to stream Ncbi, to step Checkpoint: 003730
- to stream Main, to step Merge: 000625
- to stream Main, to step Curation: 000625
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".</title><author><name sortKey="Kumar, Kishore R" sort="Kumar, Kishore R" uniqKey="Kumar K" first="Kishore R" last="Kumar">Kishore R. Kumar</name><affiliation wicri:level="1"><nlm:affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales</wicri:regionArea><wicri:noRegion>New South Wales</wicri:noRegion></affiliation></author><author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2014">2014</date><idno type="doi">10.1002/mds.25089</idno><idno type="RBID">pubmed:22753322</idno><idno type="pmid">22753322</idno><idno type="wicri:Area/PubMed/Corpus">000D16</idno><idno type="wicri:Area/PubMed/Curation">000D16</idno><idno type="wicri:Area/PubMed/Checkpoint">000641</idno><idno type="wicri:Area/Ncbi/Merge">003730</idno><idno type="wicri:Area/Ncbi/Curation">003730</idno><idno type="wicri:Area/Ncbi/Checkpoint">003730</idno><idno type="wicri:Area/Main/Merge">000625</idno><idno type="wicri:Area/Main/Curation">000625</idno><idno type="wicri:Area/Main/Exploration">000625</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".</title><author><name sortKey="Kumar, Kishore R" sort="Kumar, Kishore R" uniqKey="Kumar K" first="Kishore R" last="Kumar">Kishore R. Kumar</name><affiliation wicri:level="1"><nlm:affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia.</nlm:affiliation><country xml:lang="fr">Australie</country><wicri:regionArea>Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lübeck, Lübeck, Germany; Department of Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales</wicri:regionArea><wicri:noRegion>New South Wales</wicri:noRegion></affiliation></author><author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="eISSN">1531-8257</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Arginine (genetics)</term><term>Creutzfeldt-Jakob Syndrome (genetics)</term><term>Female</term><term>Humans</term><term>Mutation (genetics)</term><term>Prions (genetics)</term><term>Supranuclear Palsy, Progressive (physiopathology)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Arginine</term><term>Prions</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Creutzfeldt-Jakob Syndrome</term><term>Mutation</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Supranuclear Palsy, Progressive</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Female</term><term>Humans</term></keywords></textClass></profileDesc></teiHeader></TEI><affiliations><list><country><li>Australie</li></country></list><tree><noCountry><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name></noCountry><country name="Australie"><noRegion><name sortKey="Kumar, Kishore R" sort="Kumar, Kishore R" uniqKey="Kumar K" first="Kishore R" last="Kumar">Kishore R. Kumar</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000625 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000625 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= Main
|étape= Exploration
|type= RBID
|clé= pubmed:22753322
|texte= Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:22753322" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a MovDisordV3
| This area was generated with Dilib version V0.6.23. |  |