[Congenital soft tissue dysplasia. A new anatomo-clinical entity].
Identifieur interne : 005E17 ( PubMed/Checkpoint ); précédent : 005E16; suivant : 005E18[Congenital soft tissue dysplasia. A new anatomo-clinical entity].
Auteurs : D. Pellerin ; H. Martelli ; X. Latouche ; F. GasnierSource :
- Chirurgie; memoires de l'Academie de chirurgie [ 0001-4001 ] ; 1985.
Descripteurs français
- KwdFr :
- Ectoderme (anatomopathologie), Enfant, Enfant d'âge préscolaire, Femelle, Gigantisme (anatomopathologie), Hamartomes (anatomopathologie), Humains, Lymphoedème (), Malformations multiples (), Malformations multiples (anatomopathologie), Mâle, Mésoderme (anatomopathologie), Neurofibromatose de type 1 (anatomopathologie), Nourrisson, Nouveau-né, Syndrome de Klippel-Trénaunay (anatomopathologie), Tumeurs des tissus mous (anatomopathologie).
- MESH :
English descriptors
- KwdEn :
- Abnormalities, Multiple (pathology), Abnormalities, Multiple (therapy), Child, Child, Preschool, Ectoderm (pathology), Female, Gigantism (pathology), Hamartoma (pathology), Humans, Infant, Infant, Newborn, Klippel-Trenaunay-Weber Syndrome (pathology), Lymphedema (congenital), Male, Mesoderm (pathology), Neurofibromatosis 1 (pathology), Soft Tissue Neoplasms (pathology).
- MESH :
- congenital : Lymphedema.
- pathology : Abnormalities, Multiple, Ectoderm, Gigantism, Hamartoma, Klippel-Trenaunay-Weber Syndrome, Mesoderm, Neurofibromatosis 1, Soft Tissue Neoplasms.
- therapy : Abnormalities, Multiple.
- Child, Child, Preschool, Female, Humans, Infant, Infant, Newborn, Male.
PubMed: 3013512
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:3013512Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Congenital soft tissue dysplasia. A new anatomo-clinical entity].</title>
<author><name sortKey="Pellerin, D" sort="Pellerin, D" uniqKey="Pellerin D" first="D" last="Pellerin">D. Pellerin</name>
</author>
<author><name sortKey="Martelli, H" sort="Martelli, H" uniqKey="Martelli H" first="H" last="Martelli">H. Martelli</name>
</author>
<author><name sortKey="Latouche, X" sort="Latouche, X" uniqKey="Latouche X" first="X" last="Latouche">X. Latouche</name>
</author>
<author><name sortKey="Gasnier, F" sort="Gasnier, F" uniqKey="Gasnier F" first="F" last="Gasnier">F. Gasnier</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1985">1985</date>
<idno type="RBID">pubmed:3013512</idno>
<idno type="pmid">3013512</idno>
<idno type="wicri:Area/PubMed/Corpus">006882</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">006882</idno>
<idno type="wicri:Area/PubMed/Curation">006882</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">006882</idno>
<idno type="wicri:Area/PubMed/Checkpoint">006882</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">006882</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">[Congenital soft tissue dysplasia. A new anatomo-clinical entity].</title>
<author><name sortKey="Pellerin, D" sort="Pellerin, D" uniqKey="Pellerin D" first="D" last="Pellerin">D. Pellerin</name>
</author>
<author><name sortKey="Martelli, H" sort="Martelli, H" uniqKey="Martelli H" first="H" last="Martelli">H. Martelli</name>
</author>
<author><name sortKey="Latouche, X" sort="Latouche, X" uniqKey="Latouche X" first="X" last="Latouche">X. Latouche</name>
</author>
<author><name sortKey="Gasnier, F" sort="Gasnier, F" uniqKey="Gasnier F" first="F" last="Gasnier">F. Gasnier</name>
</author>
</analytic>
<series><title level="j">Chirurgie; memoires de l'Academie de chirurgie</title>
<idno type="ISSN">0001-4001</idno>
<imprint><date when="1985" type="published">1985</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abnormalities, Multiple (pathology)</term>
<term>Abnormalities, Multiple (therapy)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Ectoderm (pathology)</term>
<term>Female</term>
<term>Gigantism (pathology)</term>
<term>Hamartoma (pathology)</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Klippel-Trenaunay-Weber Syndrome (pathology)</term>
<term>Lymphedema (congenital)</term>
<term>Male</term>
<term>Mesoderm (pathology)</term>
<term>Neurofibromatosis 1 (pathology)</term>
<term>Soft Tissue Neoplasms (pathology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Ectoderme (anatomopathologie)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Gigantisme (anatomopathologie)</term>
<term>Hamartomes (anatomopathologie)</term>
<term>Humains</term>
<term>Lymphoedème ()</term>
<term>Malformations multiples ()</term>
<term>Malformations multiples (anatomopathologie)</term>
<term>Mâle</term>
<term>Mésoderme (anatomopathologie)</term>
<term>Neurofibromatose de type 1 (anatomopathologie)</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Syndrome de Klippel-Trénaunay (anatomopathologie)</term>
<term>Tumeurs des tissus mous (anatomopathologie)</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Ectoderme</term>
<term>Gigantisme</term>
<term>Hamartomes</term>
<term>Malformations multiples</term>
<term>Mésoderme</term>
<term>Neurofibromatose de type 1</term>
<term>Syndrome de Klippel-Trénaunay</term>
<term>Tumeurs des tissus mous</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Abnormalities, Multiple</term>
<term>Ectoderm</term>
<term>Gigantism</term>
<term>Hamartoma</term>
<term>Klippel-Trenaunay-Weber Syndrome</term>
<term>Mesoderm</term>
<term>Neurofibromatosis 1</term>
<term>Soft Tissue Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Abnormalities, Multiple</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Malformations multiples</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">3013512</PMID>
<DateCreated><Year>1986</Year>
<Month>08</Month>
<Day>13</Day>
</DateCreated>
<DateCompleted><Year>1986</Year>
<Month>08</Month>
<Day>13</Day>
</DateCompleted>
<DateRevised><Year>2006</Year>
<Month>11</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0001-4001</ISSN>
<JournalIssue CitedMedium="Print"><Volume>111</Volume>
<Issue>8</Issue>
<PubDate><Year>1985</Year>
</PubDate>
</JournalIssue>
<Title>Chirurgie; memoires de l'Academie de chirurgie</Title>
<ISOAbbreviation>Chirurgie</ISOAbbreviation>
</Journal>
<ArticleTitle>[Congenital soft tissue dysplasia. A new anatomo-clinical entity].</ArticleTitle>
<Pagination><MedlinePgn>667-76</MedlinePgn>
</Pagination>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Pellerin</LastName>
<ForeName>D</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y"><LastName>Martelli</LastName>
<ForeName>H</ForeName>
<Initials>H</Initials>
</Author>
<Author ValidYN="Y"><LastName>Latouche</LastName>
<ForeName>X</ForeName>
<Initials>X</Initials>
</Author>
<Author ValidYN="Y"><LastName>Gasnier</LastName>
<ForeName>F</ForeName>
<Initials>F</Initials>
</Author>
</AuthorList>
<Language>fre</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D004740">English Abstract</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<VernacularTitle>La dysplasie tissulaire congénitale. Une nouvelle entité anatomo-clinique.</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>France</Country>
<MedlineTA>Chirurgie</MedlineTA>
<NlmUniqueID>0236600</NlmUniqueID>
<ISSNLinking>0001-4001</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000015" MajorTopicYN="N">Abnormalities, Multiple</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004475" MajorTopicYN="N">Ectoderm</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005877" MajorTopicYN="N">Gigantism</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006222" MajorTopicYN="N">Hamartoma</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007223" MajorTopicYN="N">Infant</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007231" MajorTopicYN="N">Infant, Newborn</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007715" MajorTopicYN="N">Klippel-Trenaunay-Weber Syndrome</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000151" MajorTopicYN="N">congenital</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008648" MajorTopicYN="N">Mesoderm</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009456" MajorTopicYN="N">Neurofibromatosis 1</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012983" MajorTopicYN="N">Soft Tissue Neoplasms</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1985</Year>
<Month>1</Month>
<Day>1</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1985</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>1</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>1985</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">3013512</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list></list>
<tree><noCountry><name sortKey="Gasnier, F" sort="Gasnier, F" uniqKey="Gasnier F" first="F" last="Gasnier">F. Gasnier</name>
<name sortKey="Latouche, X" sort="Latouche, X" uniqKey="Latouche X" first="X" last="Latouche">X. Latouche</name>
<name sortKey="Martelli, H" sort="Martelli, H" uniqKey="Martelli H" first="H" last="Martelli">H. Martelli</name>
<name sortKey="Pellerin, D" sort="Pellerin, D" uniqKey="Pellerin D" first="D" last="Pellerin">D. Pellerin</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/PubMed/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 005E17 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 005E17 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= LymphedemaV1 |flux= PubMed |étape= Checkpoint |type= RBID |clé= pubmed:3013512 |texte= [Congenital soft tissue dysplasia. A new anatomo-clinical entity]. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i -Sk "pubmed:3013512" \ | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
![]() | This area was generated with Dilib version V0.6.31. | ![]() |