Conjugal parkinsonism - Clinical, pathology and genetic study. No evidence of person-to-person transmission.
Identifieur interne : 000402 ( Main/Exploration ); précédent : 000401; suivant : 000403Conjugal parkinsonism - Clinical, pathology and genetic study. No evidence of person-to-person transmission.
Auteurs : Ali H. Rajput [Canada] ; Leslie W. Ferguson [Canada] ; Christopher A. Robinson [Canada] ; Ilaria Guella [Canada] ; Matthew J. Farrer [Canada] ; Alexander Rajput [Canada]Source :
- Parkinsonism & related disorders [ 1873-5126 ] ; 2016.
Abstract
Neurodegeneration is known basis of several different Parkinson syndromes. The most common Parkinson syndrome is the Parkinson's disease. Distinction between different Parkinson syndromes is based on pathology or genetic findings. Recent studies indicate that several major variants of PS have some characteristics of a prion disease and may therefore be transmissible. Married couples offer a unique opportunity to study person-to-person transmission and the role of shared environments as the cause of parkinsonism.
DOI: 10.1016/j.parkreldis.2016.07.011
PubMed: 27481034
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000149
- to stream PubMed, to step Curation: 000149
- to stream PubMed, to step Checkpoint: 000149
- to stream Ncbi, to step Merge: 002041
- to stream Ncbi, to step Curation: 002041
- to stream Ncbi, to step Checkpoint: 002041
- to stream Main, to step Merge: 000403
- to stream Main, to step Curation: 000402
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Conjugal parkinsonism - Clinical, pathology and genetic study. No evidence of person-to-person transmission.</title>
<author><name sortKey="Rajput, Ali H" sort="Rajput, Ali H" uniqKey="Rajput A" first="Ali H" last="Rajput">Ali H. Rajput</name>
<affiliation wicri:level="1"><nlm:affiliation>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region, Canada. Electronic address: ali.rajput@saskatoonhealthregion.ca.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>University of Saskatchewan/Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Ferguson, Leslie W" sort="Ferguson, Leslie W" uniqKey="Ferguson L" first="Leslie W" last="Ferguson">Leslie W. Ferguson</name>
<affiliation wicri:level="1"><nlm:affiliation>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>University of Saskatchewan/Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Robinson, Christopher A" sort="Robinson, Christopher A" uniqKey="Robinson C" first="Christopher A" last="Robinson">Christopher A. Robinson</name>
<affiliation wicri:level="1"><nlm:affiliation>Division of Neuropathology, Department of Pathology, Saskatoon Health Region, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Division of Neuropathology, Department of Pathology, Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Guella, Ilaria" sort="Guella, Ilaria" uniqKey="Guella I" first="Ilaria" last="Guella">Ilaria Guella</name>
<affiliation wicri:level="1"><nlm:affiliation>Centre of Applied Neurogenetics, University of British Columbia, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Centre of Applied Neurogenetics, University of British Columbia</wicri:regionArea>
<wicri:noRegion>University of British Columbia</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
<affiliation wicri:level="1"><nlm:affiliation>Centre of Applied Neurogenetics, University of British Columbia, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Centre of Applied Neurogenetics, University of British Columbia</wicri:regionArea>
<wicri:noRegion>University of British Columbia</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Rajput, Alexander" sort="Rajput, Alexander" uniqKey="Rajput A" first="Alexander" last="Rajput">Alexander Rajput</name>
<affiliation wicri:level="1"><nlm:affiliation>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>University of Saskatchewan/Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2016">2016</date>
<idno type="RBID">pubmed:27481034</idno>
<idno type="pmid">27481034</idno>
<idno type="doi">10.1016/j.parkreldis.2016.07.011</idno>
<idno type="wicri:Area/PubMed/Corpus">000149</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000149</idno>
<idno type="wicri:Area/PubMed/Curation">000149</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000149</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000149</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000149</idno>
<idno type="wicri:Area/Ncbi/Merge">002041</idno>
<idno type="wicri:Area/Ncbi/Curation">002041</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002041</idno>
<idno type="wicri:Area/Main/Merge">000403</idno>
<idno type="wicri:Area/Main/Curation">000402</idno>
<idno type="wicri:Area/Main/Exploration">000402</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Conjugal parkinsonism - Clinical, pathology and genetic study. No evidence of person-to-person transmission.</title>
<author><name sortKey="Rajput, Ali H" sort="Rajput, Ali H" uniqKey="Rajput A" first="Ali H" last="Rajput">Ali H. Rajput</name>
<affiliation wicri:level="1"><nlm:affiliation>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region, Canada. Electronic address: ali.rajput@saskatoonhealthregion.ca.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>University of Saskatchewan/Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Ferguson, Leslie W" sort="Ferguson, Leslie W" uniqKey="Ferguson L" first="Leslie W" last="Ferguson">Leslie W. Ferguson</name>
<affiliation wicri:level="1"><nlm:affiliation>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>University of Saskatchewan/Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Robinson, Christopher A" sort="Robinson, Christopher A" uniqKey="Robinson C" first="Christopher A" last="Robinson">Christopher A. Robinson</name>
<affiliation wicri:level="1"><nlm:affiliation>Division of Neuropathology, Department of Pathology, Saskatoon Health Region, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Division of Neuropathology, Department of Pathology, Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Guella, Ilaria" sort="Guella, Ilaria" uniqKey="Guella I" first="Ilaria" last="Guella">Ilaria Guella</name>
<affiliation wicri:level="1"><nlm:affiliation>Centre of Applied Neurogenetics, University of British Columbia, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Centre of Applied Neurogenetics, University of British Columbia</wicri:regionArea>
<wicri:noRegion>University of British Columbia</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
<affiliation wicri:level="1"><nlm:affiliation>Centre of Applied Neurogenetics, University of British Columbia, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Centre of Applied Neurogenetics, University of British Columbia</wicri:regionArea>
<wicri:noRegion>University of British Columbia</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Rajput, Alexander" sort="Rajput, Alexander" uniqKey="Rajput A" first="Alexander" last="Rajput">Alexander Rajput</name>
<affiliation wicri:level="1"><nlm:affiliation>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Saskatchewan Movement Disorders Program, University of Saskatchewan/Saskatoon Health Region</wicri:regionArea>
<wicri:noRegion>University of Saskatchewan/Saskatoon Health Region</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">Parkinsonism & related disorders</title>
<idno type="eISSN">1873-5126</idno>
<imprint><date when="2016" type="published">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Neurodegeneration is known basis of several different Parkinson syndromes. The most common Parkinson syndrome is the Parkinson's disease. Distinction between different Parkinson syndromes is based on pathology or genetic findings. Recent studies indicate that several major variants of PS have some characteristics of a prion disease and may therefore be transmissible. Married couples offer a unique opportunity to study person-to-person transmission and the role of shared environments as the cause of parkinsonism.</div>
</front>
</TEI>
<affiliations><list><country><li>Canada</li>
</country>
</list>
<tree><country name="Canada"><noRegion><name sortKey="Rajput, Ali H" sort="Rajput, Ali H" uniqKey="Rajput A" first="Ali H" last="Rajput">Ali H. Rajput</name>
</noRegion>
<name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
<name sortKey="Ferguson, Leslie W" sort="Ferguson, Leslie W" uniqKey="Ferguson L" first="Leslie W" last="Ferguson">Leslie W. Ferguson</name>
<name sortKey="Guella, Ilaria" sort="Guella, Ilaria" uniqKey="Guella I" first="Ilaria" last="Guella">Ilaria Guella</name>
<name sortKey="Rajput, Alexander" sort="Rajput, Alexander" uniqKey="Rajput A" first="Alexander" last="Rajput">Alexander Rajput</name>
<name sortKey="Robinson, Christopher A" sort="Robinson, Christopher A" uniqKey="Robinson C" first="Christopher A" last="Robinson">Christopher A. Robinson</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Canada/explor/ParkinsonCanadaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000402 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000402 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Canada |area= ParkinsonCanadaV1 |flux= Main |étape= Exploration |type= RBID |clé= pubmed:27481034 |texte= Conjugal parkinsonism - Clinical, pathology and genetic study. No evidence of person-to-person transmission. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:27481034" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \ | NlmPubMed2Wicri -a ParkinsonCanadaV1
This area was generated with Dilib version V0.6.29. |