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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2002-9-5
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pubmed:abstractText |
The aims of the present study were (a) to examine the occurrence of 21-hydroxylase gene (CYP21) mutations in patients with unilateral and bilateral adrenal incidentalomas and (b) to correlate the results of mutation screening with hormonal parameters of 21-hydroxylase deficiency.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0804-4643
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
147
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
349-55
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12213672-17-alpha-Hydroxyprogesterone,
pubmed-meshheading:12213672-Adenoma,
pubmed-meshheading:12213672-Adrenal Gland Neoplasms,
pubmed-meshheading:12213672-Adrenal Hyperplasia, Congenital,
pubmed-meshheading:12213672-Adrenocorticotropic Hormone,
pubmed-meshheading:12213672-Alleles,
pubmed-meshheading:12213672-DNA,
pubmed-meshheading:12213672-DNA Mutational Analysis,
pubmed-meshheading:12213672-Female,
pubmed-meshheading:12213672-Hormones,
pubmed-meshheading:12213672-Humans,
pubmed-meshheading:12213672-Introns,
pubmed-meshheading:12213672-Male,
pubmed-meshheading:12213672-Middle Aged,
pubmed-meshheading:12213672-Polymerase Chain Reaction,
pubmed-meshheading:12213672-RNA Splicing,
pubmed-meshheading:12213672-Steroid 21-Hydroxylase
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pubmed:year |
2002
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pubmed:articleTitle |
Hormonal evaluation and mutation screening for steroid 21-hydroxylase deficiency in patients with unilateral and bilateral adrenal incidentalomas.
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pubmed:affiliation |
2nd Department of Medicine, Faculty of Medicine, Semmelweis University, H-1088 Budapest, Hungary.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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