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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1996-9-26
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pubmed:abstractText |
Presenting 3 personally examined cases, the authors underline the incidence and the characteristics of pheochromocytoma associated with Von Hippel Lindau disease. In conclusion, a systematic screening for Von Hippel Lindau disease-often unrecognized to day-must be done in every patient presenting with pheochromocytoma.
|
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 |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
609-12
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8787353-Adrenal Gland Neoplasms,
pubmed-meshheading:8787353-Adult,
pubmed-meshheading:8787353-Female,
pubmed-meshheading:8787353-Humans,
pubmed-meshheading:8787353-Middle Aged,
pubmed-meshheading:8787353-Pedigree,
pubmed-meshheading:8787353-Pheochromocytoma,
pubmed-meshheading:8787353-von Hippel-Lindau Disease
|
pubmed:year |
1995
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pubmed:articleTitle |
[Pheochromocytoma in Von Hippel Lindau disease. 3 cases].
|
pubmed:affiliation |
Clinique Endocrinologique, Hôpital de l'Antiquaille, Lyon.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|