The diverse neurological features of Niemann-Pick disease type C: a report of two cases
Identifieur interne : 009945 ( Main/Merge ); précédent : 009944; suivant : 009946The diverse neurological features of Niemann-Pick disease type C: a report of two cases
Auteurs : R. J. Coleman ; S. A. Robb ; B. D. Lake ; E. M. Brett ; A. E. HardingSource :
- Movement disorders [ 0885-3185 ] ; 1988.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Enfant.
English descriptors
- KwdEn :
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 003993
- to stream PascalFrancis, to step Curation: 002E32
- to stream PascalFrancis, to step Checkpoint: 003A31
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Pascal:90-0140310Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">The diverse neurological features of Niemann-Pick disease type C: a report of two cases</title>
<author><name sortKey="Coleman, R J" sort="Coleman, R J" uniqKey="Coleman R" first="R. J." last="Coleman">R. J. Coleman</name>
</author>
<author><name sortKey="Robb, S A" sort="Robb, S A" uniqKey="Robb S" first="S. A." last="Robb">S. A. Robb</name>
</author>
<author><name sortKey="Lake, B D" sort="Lake, B D" uniqKey="Lake B" first="B. D." last="Lake">B. D. Lake</name>
</author>
<author><name sortKey="Brett, E M" sort="Brett, E M" uniqKey="Brett E" first="E. M." last="Brett">E. M. Brett</name>
</author>
<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
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<idno type="inist">90-0140310</idno>
<date when="1988">1988</date>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">The diverse neurological features of Niemann-Pick disease type C: a report of two cases</title>
<author><name sortKey="Coleman, R J" sort="Coleman, R J" uniqKey="Coleman R" first="R. J." last="Coleman">R. J. Coleman</name>
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<author><name sortKey="Robb, S A" sort="Robb, S A" uniqKey="Robb S" first="S. A." last="Robb">S. A. Robb</name>
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<author><name sortKey="Lake, B D" sort="Lake, B D" uniqKey="Lake B" first="B. D." last="Lake">B. D. Lake</name>
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<author><name sortKey="Brett, E M" sort="Brett, E M" uniqKey="Brett E" first="E. M." last="Brett">E. M. Brett</name>
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<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
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<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="1988">1988</date>
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<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Ataxia</term>
<term>Case study</term>
<term>Cerebellum</term>
<term>Child</term>
<term>Genetic disease</term>
<term>Lipids</term>
<term>Metabolic diseases</term>
<term>Nervous system diseases</term>
<term>Niemann Pick disease</term>
<term>Symptomatology</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Sphingolipidose héréditaire Niemann Pick</term>
<term>Lipide</term>
<term>Ataxie</term>
<term>Maladie héréditaire</term>
<term>Métabolisme pathologie</term>
<term>Système nerveux pathologie</term>
<term>Cervelet</term>
<term>Symptomatologie</term>
<term>Enfant</term>
<term>Etude cas</term>
<term>Parkinson syndrome</term>
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<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Enfant</term>
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<tree><noCountry><name sortKey="Brett, E M" sort="Brett, E M" uniqKey="Brett E" first="E. M." last="Brett">E. M. Brett</name>
<name sortKey="Coleman, R J" sort="Coleman, R J" uniqKey="Coleman R" first="R. J." last="Coleman">R. J. Coleman</name>
<name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
<name sortKey="Lake, B D" sort="Lake, B D" uniqKey="Lake B" first="B. D." last="Lake">B. D. Lake</name>
<name sortKey="Robb, S A" sort="Robb, S A" uniqKey="Robb S" first="S. A." last="Robb">S. A. Robb</name>
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