Source:http://linkedlifedata.com/resource/pubmed/id/12324758
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2002-9-26
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pubmed:abstractText |
Sporadic primary hyperparathyroidism (pHPT) occurs separately and in several hereditary disorders including multiple endocrine neoplasia type 1. Irradiation to the neck, female gender, and age are well-identified risk factors that predispose to pHPT. The multiple endocrine neoplasia type 1 gene is the most commonly deranged gene in parathyroid adenomas and contains several polymorphisms including D418D with a prevalence of roughly 50%.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0039-6060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
132
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
450-5
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12324758-Aged,
pubmed-meshheading:12324758-Bone Density,
pubmed-meshheading:12324758-Female,
pubmed-meshheading:12324758-Genotype,
pubmed-meshheading:12324758-Humans,
pubmed-meshheading:12324758-Hyperparathyroidism,
pubmed-meshheading:12324758-Male,
pubmed-meshheading:12324758-Neoplasm Proteins,
pubmed-meshheading:12324758-Polymorphism, Genetic,
pubmed-meshheading:12324758-Proto-Oncogene Proteins
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pubmed:year |
2002
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pubmed:articleTitle |
Multiple endocrine neoplasia type 1 polymorphism D418D is associated with sporadic primary hyperparathyroidism.
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pubmed:affiliation |
Department of Surgical Sciences, Endocrine Unit, Uppsala University Hospital, Sweden.
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pubmed:publicationType |
Journal Article
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