More on vascular malformations.
Identifieur interne : 000981 ( Ncbi/Merge ); précédent : 000980; suivant : 000982More on vascular malformations.
Auteurs : M Michael CohenSource :
- Plastic and reconstructive surgery [ 0032-1052 ] ; 2002.
Descripteurs français
- KwdFr :
- Humains, Lymphoedème (diagnostic), Lymphoedème (génétique), Phosphohydrolase PTEN, Phosphoric monoester hydrolases (génétique), Protein Tyrosine Phosphatases, Protéines membranaires, Syndrome, Syndrome de Klippel-Trénaunay (diagnostic), Syndrome de Klippel-Trénaunay (génétique), Vaisseaux sanguins (malformations).
- MESH :
- diagnostic : Lymphoedème, Syndrome de Klippel-Trénaunay.
- génétique : Lymphoedème, Phosphoric monoester hydrolases, Syndrome de Klippel-Trénaunay.
- malformations : Vaisseaux sanguins.
- Humains, Phosphohydrolase PTEN, Protein Tyrosine Phosphatases, Protéines membranaires, Syndrome.
English descriptors
- KwdEn :
- Blood Vessels (abnormalities), Humans, Klippel-Trenaunay-Weber Syndrome (diagnosis), Klippel-Trenaunay-Weber Syndrome (genetics), Lymphedema (diagnosis), Lymphedema (genetics), Membrane Proteins, PTEN Phosphohydrolase, Phosphoric Monoester Hydrolases (genetics), Protein Tyrosine Phosphatases, Syndrome.
- MESH :
- chemical , genetics : Phosphoric Monoester Hydrolases.
- chemical : Membrane Proteins, PTEN Phosphohydrolase, Protein Tyrosine Phosphatases.
- abnormalities : Blood Vessels.
- diagnosis : Klippel-Trenaunay-Weber Syndrome, Lymphedema.
- genetics : Klippel-Trenaunay-Weber Syndrome, Lymphedema.
- Humans, Syndrome.
PubMed: 12045604
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 004568
- to stream PubMed, to step Curation: 004568
- to stream PubMed, to step Checkpoint: 004568
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pubmed:12045604Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Blood Vessels (abnormalities)</term>
<term>Humans</term>
<term>Klippel-Trenaunay-Weber Syndrome (diagnosis)</term>
<term>Klippel-Trenaunay-Weber Syndrome (genetics)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (genetics)</term>
<term>Membrane Proteins</term>
<term>PTEN Phosphohydrolase</term>
<term>Phosphoric Monoester Hydrolases (genetics)</term>
<term>Protein Tyrosine Phosphatases</term>
<term>Syndrome</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Humains</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (génétique)</term>
<term>Phosphohydrolase PTEN</term>
<term>Phosphoric monoester hydrolases (génétique)</term>
<term>Protein Tyrosine Phosphatases</term>
<term>Protéines membranaires</term>
<term>Syndrome</term>
<term>Syndrome de Klippel-Trénaunay (diagnostic)</term>
<term>Syndrome de Klippel-Trénaunay (génétique)</term>
<term>Vaisseaux sanguins (malformations)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Phosphoric Monoester Hydrolases</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Membrane Proteins</term>
<term>PTEN Phosphohydrolase</term>
<term>Protein Tyrosine Phosphatases</term>
</keywords>
<keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Blood Vessels</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Klippel-Trenaunay-Weber Syndrome</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphoedème</term>
<term>Syndrome de Klippel-Trénaunay</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Klippel-Trenaunay-Weber Syndrome</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphoedème</term>
<term>Phosphoric monoester hydrolases</term>
<term>Syndrome de Klippel-Trénaunay</term>
</keywords>
<keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Vaisseaux sanguins</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Humains</term>
<term>Phosphohydrolase PTEN</term>
<term>Protein Tyrosine Phosphatases</term>
<term>Protéines membranaires</term>
<term>Syndrome</term>
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<Month>06</Month>
<Day>04</Day>
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<DateCompleted><Year>2002</Year>
<Month>06</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised><Year>2016</Year>
<Month>11</Month>
<Day>24</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0032-1052</ISSN>
<JournalIssue CitedMedium="Print"><Volume>109</Volume>
<Issue>7</Issue>
<PubDate><Year>2002</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Plastic and reconstructive surgery</Title>
<ISOAbbreviation>Plast. Reconstr. Surg.</ISOAbbreviation>
</Journal>
<ArticleTitle>More on vascular malformations.</ArticleTitle>
<Pagination><MedlinePgn>2591-4; author reply 2594-5</MedlinePgn>
</Pagination>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Cohen</LastName>
<ForeName>M Michael</ForeName>
<Initials>MM</Initials>
<Suffix>Jr</Suffix>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Plast Reconstr Surg</MedlineTA>
<NlmUniqueID>1306050</NlmUniqueID>
<ISSNLinking>0032-1052</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008565">Membrane Proteins</NameOfSubstance>
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<Chemical><RegistryNumber>EC 3.1.3.2</RegistryNumber>
<NameOfSubstance UI="D010744">Phosphoric Monoester Hydrolases</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.1.3.48</RegistryNumber>
<NameOfSubstance UI="D017027">Protein Tyrosine Phosphatases</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.1.3.48</RegistryNumber>
<NameOfSubstance UI="C446603">TPTE protein, human</NameOfSubstance>
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<Chemical><RegistryNumber>EC 3.1.3.67</RegistryNumber>
<NameOfSubstance UI="D051059">PTEN Phosphohydrolase</NameOfSubstance>
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<CitationSubset>AIM</CitationSubset>
<CitationSubset>IM</CitationSubset>
<CommentsCorrectionsList><CommentsCorrections RefType="CommentOn"><RefSource>Plast Reconstr Surg. 2001 May;107(6):1509-23</RefSource>
<PMID Version="1">11335828</PMID>
</CommentsCorrections>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D001808" MajorTopicYN="N">Blood Vessels</DescriptorName>
<QualifierName UI="Q000002" MajorTopicYN="Y">abnormalities</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007715" MajorTopicYN="N">Klippel-Trenaunay-Weber Syndrome</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008565" MajorTopicYN="Y">Membrane Proteins</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D051059" MajorTopicYN="N">PTEN Phosphohydrolase</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010744" MajorTopicYN="N">Phosphoric Monoester Hydrolases</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017027" MajorTopicYN="Y">Protein Tyrosine Phosphatases</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName>
</MeshHeading>
</MeshHeadingList>
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