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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
|
pubmed:dateCreated |
1979-8-16
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pubmed:abstractText |
Endocrine features associated with the primary empty sella turcica syndrom are rare; they are usually related to a pituitary microadenoma and more rarely to an idiopathic panhypop ituitarism. A pituitary dwarfism with an idiopathic panhypopituitarism of hypothalamic origin, associated with an "empty" sella turcica containing functional and stimulable pituitary tissue, is reported in a 27 year old male Moraccan.
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
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pubmed:issn |
0301-1518
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
10
|
pubmed:volume |
8
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
847-8, 850
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:450657-Adult,
pubmed-meshheading:450657-Dwarfism, Pituitary,
pubmed-meshheading:450657-Empty Sella Syndrome,
pubmed-meshheading:450657-Humans,
pubmed-meshheading:450657-Hypopituitarism,
pubmed-meshheading:450657-Hypothalamus,
pubmed-meshheading:450657-Male,
pubmed-meshheading:450657-Pneumoencephalography
|
pubmed:year |
1979
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pubmed:articleTitle |
[Panhypopituitarism and dwarfism in a man with a primary empty sella turcica (author's transl)].
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|