pubmed-article:2889861 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2889861 | lifeskim:mentions | umls-concept:C0016751 | lld:lifeskim |
pubmed-article:2889861 | lifeskim:mentions | umls-concept:C0024487 | lld:lifeskim |
pubmed-article:2889861 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:2889861 | lifeskim:mentions | umls-concept:C1524063 | lld:lifeskim |
pubmed-article:2889861 | lifeskim:mentions | umls-concept:C1553628 | lld:lifeskim |
pubmed-article:2889861 | pubmed:issue | 8565 | lld:pubmed |
pubmed-article:2889861 | pubmed:dateCreated | 1987-11-27 | lld:pubmed |
pubmed-article:2889861 | pubmed:abstractText | The effect of fructose on liver metabolism in patients with hereditary fructose intolerance (HFI) and in heterozygotes for HFI was studied by 31P magnetic resonance spectroscopy (31P-MRS). In patients with HFI (n = 5) ingestion of small amounts of fructose was followed by an increase in sugar phosphates and decrease in inorganic phosphate (Pi) in the liver that could be detected by 31P-MRS. 31P-MRS could be used to diagnose fructose intolerance and to monitor the patients' compliance with a fructose-restricted diet. In heterozygotes (n = 8) 50 g fructose given orally led to accumulation of sugar phosphates and depletion of Pi in the liver. Fructose also induced a larger increase in plasma urate in heterozygotes than in control subjects. The effect of fructose on liver Pi and plasma urate was most pronounced in heterozygotes with gout (n = 3). Heterozygosity for HFI may predispose to hyperuricaemia. | lld:pubmed |
pubmed-article:2889861 | pubmed:language | eng | lld:pubmed |
pubmed-article:2889861 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2889861 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:2889861 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2889861 | pubmed:month | Oct | lld:pubmed |
pubmed-article:2889861 | pubmed:issn | 0140-6736 | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:RaddaG KGK | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:HerschkowitzN... | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:SchwarzHH | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:TaylorD JDJ | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:LeonardJ VJV | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:CollinsJ EJE | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:RajagopalanBB | lld:pubmed |
pubmed-article:2889861 | pubmed:author | pubmed-author:OberhaensliR... | lld:pubmed |
pubmed-article:2889861 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2889861 | pubmed:day | 24 | lld:pubmed |
pubmed-article:2889861 | pubmed:volume | 2 | lld:pubmed |
pubmed-article:2889861 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2889861 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2889861 | pubmed:pagination | 931-4 | lld:pubmed |
pubmed-article:2889861 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:2889861 | pubmed:year | 1987 | lld:pubmed |
pubmed-article:2889861 | pubmed:articleTitle | Study of hereditary fructose intolerance by use of 31P magnetic resonance spectroscopy. | lld:pubmed |
pubmed-article:2889861 | pubmed:affiliation | MRC Clinical Magnetic Resonance Facility, John Radcliffe Hospital, Oxford. | lld:pubmed |
pubmed-article:2889861 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2889861 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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