[Description of a case of sporadic congenital lymphedema associated with chronic steatorrhea].
Identifieur interne : 010B79 ( Main/Exploration ); précédent : 010B78; suivant : 010B80[Description of a case of sporadic congenital lymphedema associated with chronic steatorrhea].
Auteurs : M. MasaroneSource :
- Minerva pediatrica [ 0026-4946 ] ; 1970.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- complications : Celiac Disease, Lymphangiectasis, Protein-Losing Enteropathies.
- congenital : Lymphedema.
- Humans, Infant, Lipid Metabolism, Male.
PubMed: 5436274
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 007830
- to stream PubMed, to step Curation: 007830
- to stream PubMed, to step Checkpoint: 007830
- to stream Ncbi, to step Merge: 00A440
- to stream Ncbi, to step Curation: 00A440
- to stream Ncbi, to step Checkpoint: 00A440
- to stream Main, to step Merge: 011C44
- to stream Main, to step Curation: 010B79
Le document en format XML
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<author><name sortKey="Masarone, M" sort="Masarone, M" uniqKey="Masarone M" first="M" last="Masarone">M. Masarone</name>
</author>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[Description of a case of sporadic congenital lymphedema associated with chronic steatorrhea].</title>
<author><name sortKey="Masarone, M" sort="Masarone, M" uniqKey="Masarone M" first="M" last="Masarone">M. Masarone</name>
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<series><title level="j">Minerva pediatrica</title>
<idno type="ISSN">0026-4946</idno>
<imprint><date when="1970" type="published">1970</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Celiac Disease (complications)</term>
<term>Humans</term>
<term>Infant</term>
<term>Lipid Metabolism</term>
<term>Lymphangiectasis (complications)</term>
<term>Lymphedema (congenital)</term>
<term>Male</term>
<term>Protein-Losing Enteropathies (complications)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Entéropathie exsudative ()</term>
<term>Humains</term>
<term>Lymphangiectasie ()</term>
<term>Lymphoedème ()</term>
<term>Maladie coeliaque ()</term>
<term>Mâle</term>
<term>Métabolisme des lipides</term>
<term>Nourrisson</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Celiac Disease</term>
<term>Lymphangiectasis</term>
<term>Protein-Losing Enteropathies</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
<term>Infant</term>
<term>Lipid Metabolism</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Entéropathie exsudative</term>
<term>Humains</term>
<term>Lymphangiectasie</term>
<term>Lymphoedème</term>
<term>Maladie coeliaque</term>
<term>Mâle</term>
<term>Métabolisme des lipides</term>
<term>Nourrisson</term>
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<affiliations><list></list>
<tree><noCountry><name sortKey="Masarone, M" sort="Masarone, M" uniqKey="Masarone M" first="M" last="Masarone">M. Masarone</name>
</noCountry>
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</record>
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