LymphedemaV1, Main, Exploration, bibRecordById, pubmed:6485790

Aagenaes's syndrome in an Italian child

Identifieur interne : 00F321 ( Main/Exploration ); précédent : 00F320; suivant : 00F322

Aagenaes's syndrome in an Italian child

Auteurs : P. Vajro ; A. Romano ; A. Fontanella ; V. Oggero ; R. Vecchione ; D. H. Shmerling

Source :

Acta paediatrica scandinavica [ 0001-656X ] ; 1984.

RBID : Pascal:85-0102169

Descripteurs français

KwdFr :
- Cholestase (diagnostic), Cholestase (génétique), Enfant, Femelle, Humains, Italie, Lymphoedème (diagnostic), Lymphoedème (génétique), Récidive, Syndrome.
MESH :
- diagnostic : Cholestase, Lymphoedème.
- génétique : Cholestase, Lymphoedème.
Pascal (Inist)
- Cholostase intrahépatique, Enfant, Femelle, Humains, Héréditaire, Italie, Récidivant, Lymphoedème, Enfant, Italie, Lymphatique pathologie, Foie voie biliaire pathologie, Appareil digestif pathologie, Aagenaes syndrome, Récidive, Syndrome.
Wicri :
- geographic : Italie.
- topic : Enfant.

English descriptors

KwdEn :
- Child, Cholestasis (diagnosis), Cholestasis (genetics), Digestive diseases, Female, Hepatobiliary disease, Hereditary, Humans, Intrahepatic cholostasis, Italy, Lymphatic vessel disease, Lymphedema, Lymphedema (diagnosis), Lymphedema (genetics), Recurrence, Recurrent, Syndrome.
MESH :
- geographic : Italy.
- diagnosis : Cholestasis, Lymphedema.
- genetics : Cholestasis, Lymphedema.
- Child, Female, Humans, Recurrence, Syndrome.

Abstract

Le syndrome d'Aagenaes, cholostase héréditaire récidivante avec lymphœdème, est rare, ou en rapporte un cas chez un enfant italien et suggère que cette affection soit plus souvent considérée dans le diagnostic différentiel de la cholostase infantile idiopathique

Affiliations:

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Aagenaes's syndrome in an Italian child</title>
<author><name sortKey="Vajro, P" sort="Vajro, P" uniqKey="Vajro P" first="P." last="Vajro">P. Vajro</name>
</author>
<author><name sortKey="Romano, A" sort="Romano, A" uniqKey="Romano A" first="A." last="Romano">A. Romano</name>
</author>
<author><name sortKey="Fontanella, A" sort="Fontanella, A" uniqKey="Fontanella A" first="A." last="Fontanella">A. Fontanella</name>
</author>
<author><name sortKey="Oggero, V" sort="Oggero, V" uniqKey="Oggero V" first="V." last="Oggero">V. Oggero</name>
</author>
<author><name sortKey="Vecchione, R" sort="Vecchione, R" uniqKey="Vecchione R" first="R." last="Vecchione">R. Vecchione</name>
</author>
<author><name sortKey="Shmerling, D H" sort="Shmerling, D H" uniqKey="Shmerling D" first="D. H." last="Shmerling">D. H. Shmerling</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">85-0102169</idno>
<date when="1984">1984</date>
<idno type="stanalyst">PASCAL 85-0102169 INIST</idno>
<idno type="RBID">Pascal:85-0102169</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">001115</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000993</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">001122</idno>
<idno type="wicri:explorRef" wicri:stream="PascalFrancis" wicri:step="Checkpoint">001122</idno>
<idno type="wicri:doubleKey">0001-656X:1984:Vajro P:aagenaes:s:syndrome</idno>
<idno type="wicri:Area/Main/Merge">010193</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:6485790</idno>
<idno type="wicri:Area/PubMed/Corpus">006923</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">006923</idno>
<idno type="wicri:Area/PubMed/Curation">006923</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">006923</idno>
<idno type="wicri:Area/PubMed/Checkpoint">006923</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">006923</idno>
<idno type="wicri:Area/Ncbi/Merge">00AA83</idno>
<idno type="wicri:Area/Ncbi/Curation">00AA83</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">00AA83</idno>
<idno type="wicri:doubleKey">0001-656X:1984:Vajro P:aagenaes:s:syndrome</idno>
<idno type="wicri:Area/Main/Merge">010012</idno>
<idno type="wicri:Area/Main/Curation">00F321</idno>
<idno type="wicri:Area/Main/Exploration">00F321</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Aagenaes's syndrome in an Italian child</title>
<author><name sortKey="Vajro, P" sort="Vajro, P" uniqKey="Vajro P" first="P." last="Vajro">P. Vajro</name>
</author>
<author><name sortKey="Romano, A" sort="Romano, A" uniqKey="Romano A" first="A." last="Romano">A. Romano</name>
</author>
<author><name sortKey="Fontanella, A" sort="Fontanella, A" uniqKey="Fontanella A" first="A." last="Fontanella">A. Fontanella</name>
</author>
<author><name sortKey="Oggero, V" sort="Oggero, V" uniqKey="Oggero V" first="V." last="Oggero">V. Oggero</name>
</author>
<author><name sortKey="Vecchione, R" sort="Vecchione, R" uniqKey="Vecchione R" first="R." last="Vecchione">R. Vecchione</name>
</author>
<author><name sortKey="Shmerling, D H" sort="Shmerling, D H" uniqKey="Shmerling D" first="D. H." last="Shmerling">D. H. Shmerling</name>
</author>
</analytic>
<series><title level="j" type="main">Acta paediatrica scandinavica</title>
<title level="j" type="abbreviated">Acta Paediatr. Scand.</title>
<idno type="ISSN">0001-656X</idno>
<imprint><date when="1984">1984</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Acta paediatrica scandinavica</title>
<title level="j" type="abbreviated">Acta Paediatr. Scand.</title>
<idno type="ISSN">0001-656X</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Child</term>
<term>Cholestasis (diagnosis)</term>
<term>Cholestasis (genetics)</term>
<term>Digestive diseases</term>
<term>Female</term>
<term>Hepatobiliary disease</term>
<term>Hereditary</term>
<term>Humans</term>
<term>Intrahepatic cholostasis</term>
<term>Italy</term>
<term>Lymphatic vessel disease</term>
<term>Lymphedema</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (genetics)</term>
<term>Recurrence</term>
<term>Recurrent</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Cholestase (diagnostic)</term>
<term>Cholestase (génétique)</term>
<term>Enfant</term>
<term>Femelle</term>
<term>Humains</term>
<term>Italie</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (génétique)</term>
<term>Récidive</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>Italy</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cholestasis</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Cholestase</term>
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Cholestasis</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Cholestase</term>
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child</term>
<term>Female</term>
<term>Humans</term>
<term>Recurrence</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Cholostase intrahépatique</term>
<term>Enfant</term>
<term>Femelle</term>
<term>Humains</term>
<term>Héréditaire</term>
<term>Italie</term>
<term>Récidivant</term>
<term>Lymphoedème</term>
<term>Enfant</term>
<term>Italie</term>
<term>Lymphatique pathologie</term>
<term>Foie voie biliaire pathologie</term>
<term>Appareil digestif pathologie</term>
<term>Aagenaes syndrome</term>
<term>Récidive</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Italie</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Enfant</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="fr">Le syndrome d'Aagenaes, cholostase héréditaire récidivante avec lymphœdème, est rare, ou en rapporte un cas chez un enfant italien et suggère que cette affection soit plus souvent considérée dans le diagnostic différentiel de la cholostase infantile idiopathique</div>
</front>
</TEI>
<affiliations><list></list>
<tree><noCountry><name sortKey="Fontanella, A" sort="Fontanella, A" uniqKey="Fontanella A" first="A." last="Fontanella">A. Fontanella</name>
<name sortKey="Oggero, V" sort="Oggero, V" uniqKey="Oggero V" first="V." last="Oggero">V. Oggero</name>
<name sortKey="Romano, A" sort="Romano, A" uniqKey="Romano A" first="A." last="Romano">A. Romano</name>
<name sortKey="Shmerling, D H" sort="Shmerling, D H" uniqKey="Shmerling D" first="D. H." last="Shmerling">D. H. Shmerling</name>
<name sortKey="Vajro, P" sort="Vajro, P" uniqKey="Vajro P" first="P." last="Vajro">P. Vajro</name>
<name sortKey="Vecchione, R" sort="Vecchione, R" uniqKey="Vecchione R" first="R." last="Vecchione">R. Vecchione</name>
</noCountry>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 00F321 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 00F321 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     Pascal:85-0102169
   |texte=   Aagenaes's syndrome in an Italian child
}}

This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024

Serveur d'exploration sur le lymphœdème

Aagenaes's syndrome in an Italian child

Aagenaes's syndrome in an Italian child

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Serveur d'exploration sur le lymphœdème
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.