| pubmed-article:8487506 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8487506 | lifeskim:mentions | umls-concept:C0016751 | lld:lifeskim |
| pubmed-article:8487506 | lifeskim:mentions | umls-concept:C1533148 | lld:lifeskim |
| pubmed-article:8487506 | lifeskim:mentions | umls-concept:C0205374 | lld:lifeskim |
| pubmed-article:8487506 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:8487506 | pubmed:dateCreated | 1993-6-7 | lld:pubmed |
| pubmed-article:8487506 | 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. | lld:pubmed |
| pubmed-article:8487506 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8487506 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8487506 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8487506 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8487506 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8487506 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8487506 | pubmed:issn | 0141-8955 | lld:pubmed |
| pubmed-article:8487506 | pubmed:author | pubmed-author:AdamsAA | lld:pubmed |
| pubmed-article:8487506 | pubmed:author | pubmed-author:Catto-SmithA... | lld:pubmed |
| pubmed-article:8487506 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8487506 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:8487506 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8487506 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8487506 | pubmed:pagination | 73-7 | lld:pubmed |
| pubmed-article:8487506 | pubmed:dateRevised | 2007-3-21 | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:meshHeading | pubmed-meshheading:8487506-... | lld:pubmed |
| pubmed-article:8487506 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8487506 | pubmed:articleTitle | A possible case of transient hereditary fructose intolerance. | lld:pubmed |
| pubmed-article:8487506 | pubmed:affiliation | Department of Gastroenterology, Royal Children's Hospital, Parkville, Victoria, Australia. | lld:pubmed |
| pubmed-article:8487506 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8487506 | pubmed:publicationType | Case Reports | lld:pubmed |
