Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2007-10-16
pubmed:abstractText
The diagnosis of acromegaly requires a glucose-suppressed growth hormone (GH) nadir greater than 1 microg/l associated with clinical symptoms and signs. Here, we present a patient who has acromegalic clinical findings associated with a nadir GH level < 1 microg/l during an oral glucose tolerance test.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0334-018X
pubmed:author
pubmed:issnType
Print
pubmed:volume
20
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
945-9
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Acromegaly symptoms without pituitary adenoma in an adolescent.
pubmed:affiliation
Department of Pediatric Endocrinology, Ondokuz Mayis University Medical Faculty, Kurupelit, Samsun, Turkey. aylaguven@yahoo.com
pubmed:publicationType
Journal Article, Case Reports