[You make the diagnosis: congenital hereditary lymphedema].
Identifieur interne : 00F060 ( Main/Exploration ); précédent : 00F059; suivant : 00F061[You make the diagnosis: congenital hereditary lymphedema].
Auteurs : P H Schober ; M. Kratky ; W D MüllerSource :
- Padiatrie und Padologie [ 0030-9338 ] ; 1984.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphoedème.
- génétique : Lymphoedème.
- Diagnostic différentiel, Humains, Mâle, Nouveau-né.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Lymphedema.
- genetics : Lymphedema.
- Diagnosis, Differential, Humans, Infant, Newborn, Male.
PubMed: 6504549
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 006A00
- to stream PubMed, to step Curation: 006A00
- to stream PubMed, to step Checkpoint: 006A00
- to stream Ncbi, to step Merge: 00AA91
- to stream Ncbi, to step Curation: 00AA91
- to stream Ncbi, to step Checkpoint: 00AA91
- to stream Main, to step Merge: 00FE95
- to stream Main, to step Curation: 00F060
Le document en format XML
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<author><name sortKey="Schober, P H" sort="Schober, P H" uniqKey="Schober P" first="P H" last="Schober">P H Schober</name>
</author>
<author><name sortKey="Kratky, M" sort="Kratky, M" uniqKey="Kratky M" first="M" last="Kratky">M. Kratky</name>
</author>
<author><name sortKey="Muller, W D" sort="Muller, W D" uniqKey="Muller W" first="W D" last="Müller">W D Müller</name>
</author>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[You make the diagnosis: congenital hereditary lymphedema].</title>
<author><name sortKey="Schober, P H" sort="Schober, P H" uniqKey="Schober P" first="P H" last="Schober">P H Schober</name>
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<author><name sortKey="Kratky, M" sort="Kratky, M" uniqKey="Kratky M" first="M" last="Kratky">M. Kratky</name>
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<series><title level="j">Padiatrie und Padologie</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Infant, Newborn</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (genetics)</term>
<term>Male</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Diagnostic différentiel</term>
<term>Humains</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (génétique)</term>
<term>Mâle</term>
<term>Nouveau-né</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphoedème</term>
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<term>Humans</term>
<term>Infant, Newborn</term>
<term>Male</term>
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<term>Humains</term>
<term>Mâle</term>
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<name sortKey="Schober, P H" sort="Schober, P H" uniqKey="Schober P" first="P H" last="Schober">P H Schober</name>
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