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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1980-9-23
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pubmed:abstractText |
Feminizing tumour of adrenals are rare. Gynecomasty, abdominal tumour are the more frequently observed symptoms. The described case in a 38 years aged man is of special interest because of association with primary hyperaldosteronism. Studies in vivo and in vitro are reported. In vitro studies shown a high 18 hydroxylation biosynthetic activity of tumoral fragment and a great synthesis of polar phenolsteroids with testosterone as precurseurs.
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pubmed:language |
fre
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0003-4266
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
65-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7396400-Adrenal Cortex Neoplasms,
pubmed-meshheading:7396400-Adult,
pubmed-meshheading:7396400-Feminization,
pubmed-meshheading:7396400-Humans,
pubmed-meshheading:7396400-Hydroxylation,
pubmed-meshheading:7396400-Hyperaldosteronism,
pubmed-meshheading:7396400-Hypertension,
pubmed-meshheading:7396400-Male
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pubmed:articleTitle |
[Malignant tumour of adrenal with feminizing syndrome and primary hyperaldosteronism (author's transl)].
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pubmed:publicationType |
Journal Article,
In Vitro,
English Abstract
|