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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5 Suppl
|
| pubmed:dateCreated |
1993-11-23
|
| pubmed:abstractText |
A review is presented of genetic defects affecting fructose metabolism in humans. Presently, six conditions have been recognized: fructose malabsorption, fructokinase deficiency, aldolase A and aldolase B deficiency, fructose-1,6-diphosphatase deficiency and D-glyceric aciduria. Clinical presentations of these conditions, enzymatic and/or molecular defects, pathophysiological consequences, and modes of treatments are discussed.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Nov
|
| pubmed:issn |
0002-9165
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
58
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
788S-795S
|
| pubmed:dateRevised |
2005-11-16
|
| pubmed:meshHeading |
pubmed-meshheading:8213611-Fructokinases,
pubmed-meshheading:8213611-Fructose Metabolism, Inborn Errors,
pubmed-meshheading:8213611-Fructose-1,6-Diphosphatase Deficiency,
pubmed-meshheading:8213611-Fructose-Bisphosphate Aldolase,
pubmed-meshheading:8213611-Humans,
pubmed-meshheading:8213611-Malabsorption Syndromes
|
| pubmed:year |
1993
|
| pubmed:articleTitle |
Inborn errors of fructose metabolism.
|
| pubmed:affiliation |
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta.
|
| pubmed:publicationType |
Journal Article,
Review
|