Lymphangiogenesis and lymphologic syndromes.
Identifieur interne : 009A10 ( Ncbi/Merge ); précédent : 009A09; suivant : 009A11Lymphangiogenesis and lymphologic syndromes.
Auteurs : M H Witte ; C L WitteSource :
- Lymphology [ 0024-7766 ] ; 1986.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Femelle, Foetus (physiopathologie), Humains, Lymphangiectasie (physiopathologie), Lymphangiome (physiopathologie), Lymphangiosarcome (physiopathologie), Lymphographie (), Maladies lymphatiques (physiopathologie), Mâle, Nouveau-né, Poumon (physiopathologie), Syndrome de Turner (diagnostic), Syndrome de Turner (génétique), Système lymphatique (croissance et développement), Système lymphatique (physiopathologie).
- MESH :
- croissance et développement : Système lymphatique.
- diagnostic : Syndrome de Turner.
- génétique : Syndrome de Turner.
- physiopathologie : Foetus, Lymphangiectasie, Lymphangiome, Lymphangiosarcome, Maladies lymphatiques, Poumon, Système lymphatique.
- Adolescent, Adulte, Femelle, Humains, Lymphographie, Mâle, Nouveau-né.
English descriptors
- KwdEn :
- Adolescent, Adult, Female, Fetus (physiopathology), Humans, Infant, Newborn, Lung (physiopathology), Lymphangiectasis (physiopathology), Lymphangioma (physiopathology), Lymphangiosarcoma (physiopathology), Lymphatic Diseases (physiopathology), Lymphatic System (growth & development), Lymphatic System (physiopathology), Lymphography (methods), Male, Turner Syndrome (diagnosis), Turner Syndrome (genetics).
- MESH :
- diagnosis : Turner Syndrome.
- genetics : Turner Syndrome.
- growth & development : Lymphatic System.
- methods : Lymphography.
- physiopathology : Fetus, Lung, Lymphangiectasis, Lymphangioma, Lymphangiosarcoma, Lymphatic Diseases, Lymphatic System.
- Adolescent, Adult, Female, Humans, Infant, Newborn, Male.
Abstract
A unifying concept linking disorders of lymphatic dysplasia, hyperplasia and neoplasia is presented. The central role of disturbed lymphangiogenesis is illustrated in a wide variety of lymphologic syndromes characterized by lymphedema, lymphangiectasia, lymphangioma, and lymphangiosarcoma.
PubMed: 3724235
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pubmed:3724235Le document en format XML
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The central role of disturbed lymphangiogenesis is illustrated in a wide variety of lymphologic syndromes characterized by lymphedema, lymphangiectasia, lymphangioma, and lymphangiosarcoma.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">3724235</PMID><DateCreated><Year>1986</Year><Month>08</Month><Day>12</Day></DateCreated><DateCompleted><Year>1986</Year><Month>08</Month><Day>12</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0024-7766</ISSN><JournalIssue CitedMedium="Print"><Volume>19</Volume><Issue>1</Issue><PubDate><Year>1986</Year><Month>Mar</Month></PubDate></JournalIssue><Title>Lymphology</Title><ISOAbbreviation>Lymphology</ISOAbbreviation></Journal><ArticleTitle>Lymphangiogenesis and lymphologic syndromes.</ArticleTitle><Pagination><MedlinePgn>21-8</MedlinePgn></Pagination><Abstract><AbstractText>A unifying concept linking disorders of lymphatic dysplasia, hyperplasia and neoplasia is presented. The central role of disturbed lymphangiogenesis is illustrated in a wide variety of lymphologic syndromes characterized by lymphedema, lymphangiectasia, lymphangioma, and lymphangiosarcoma.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Witte</LastName><ForeName>M H</ForeName><Initials>MH</Initials></Author><Author ValidYN="Y"><LastName>Witte</LastName><ForeName>C L</ForeName><Initials>CL</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Lymphology</MedlineTA><NlmUniqueID>0155112</NlmUniqueID><ISSNLinking>0024-7766</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005333" MajorTopicYN="N">Fetus</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007231" MajorTopicYN="N">Infant, Newborn</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008168" MajorTopicYN="N">Lung</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008200" MajorTopicYN="N">Lymphangiectasis</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008202" MajorTopicYN="N">Lymphangioma</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008206" MajorTopicYN="N">Lymphatic Diseases</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="Y">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008208" MajorTopicYN="N">Lymphatic System</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008220" MajorTopicYN="N">Lymphography</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014424" MajorTopicYN="N">Turner Syndrome</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1986</Year><Month>3</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1986</Year><Month>3</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1986</Year><Month>3</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">3724235</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Witte, C L" sort="Witte, C L" uniqKey="Witte C" first="C L" last="Witte">C L Witte</name><name sortKey="Witte, M H" sort="Witte, M H" uniqKey="Witte M" first="M H" last="Witte">M H Witte</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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