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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2008-4-16
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pubmed:abstractText |
Adult-onset non-insulinoma persistent hyperinsulinaemic hypoglycaemia (NI-PHH) and the variant NI-pancreatogenous hypoglycaemia syndrome (NIPHS) are genetically unexplained diseases, without reports of hypoglycaemia unawareness or familial inheritance.
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pubmed:commentsCorrections |
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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 |
May
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pubmed:issn |
1365-2265
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
747-55
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pubmed:dateRevised |
2009-9-29
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pubmed:meshHeading |
pubmed-meshheading:18208578-Adolescent,
pubmed-meshheading:18208578-Adult,
pubmed-meshheading:18208578-Female,
pubmed-meshheading:18208578-Genetic Predisposition to Disease,
pubmed-meshheading:18208578-Glucokinase,
pubmed-meshheading:18208578-Humans,
pubmed-meshheading:18208578-Hyperinsulinism,
pubmed-meshheading:18208578-Hypoglycemia,
pubmed-meshheading:18208578-Insulinoma,
pubmed-meshheading:18208578-Male,
pubmed-meshheading:18208578-Middle Aged,
pubmed-meshheading:18208578-Mutation,
pubmed-meshheading:18208578-Young Adult
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pubmed:year |
2008
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pubmed:articleTitle |
Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation: hypoglycaemia unawareness and attacks.
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pubmed:affiliation |
Department of Paediatrics, Odense University Hospital, Denmark. henrik.christesen@ouh.regionsyddanmark.dk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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