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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1993-6-7
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pubmed:abstractText |
A patient is described who presented with the signs and symptoms of hereditary fructose intolerance a few hours after her first fructose challenge. The diagnosis was confirmed by the demonstration of reduced activity of hepatic aldolase B towards fructose-1-phosphate. A second liver biopsy 10 months later had normal aldolase B activity towards fructose-1-phosphate and a fructose tolerance test was also normal. A possible explanation for these findings is proposed.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
0141-8955
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
16
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
73-7
|
pubmed:dateRevised |
2007-3-21
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pubmed:meshHeading |
pubmed-meshheading:8487506-Female,
pubmed-meshheading:8487506-Fructose Intolerance,
pubmed-meshheading:8487506-Fructose-Bisphosphate Aldolase,
pubmed-meshheading:8487506-Fructosephosphates,
pubmed-meshheading:8487506-Humans,
pubmed-meshheading:8487506-Infant,
pubmed-meshheading:8487506-Infant Food,
pubmed-meshheading:8487506-Liver
|
pubmed:year |
1993
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pubmed:articleTitle |
A possible case of transient hereditary fructose intolerance.
|
pubmed:affiliation |
Department of Gastroenterology, Royal Children's Hospital, Parkville, Victoria, Australia.
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pubmed:publicationType |
Journal Article,
Case Reports
|