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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1990-11-9
|
| pubmed:abstractText |
A case of primary hyperoxaluria is presented. In a product of consanguinous marriage recurrent stone formation, nephrocalcinosis and increased urinary oxalate excretion revealed the diagnosis of hyperoxaluria. Diagnosis and treatment of primary hyperoxaluria are briefly reviewed and the importance of elevated urinary oxalate level in diagnosis is emphasized.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0301-1623
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
22
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
223-6
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:2210975-Calcium Oxalate,
pubmed-meshheading:2210975-Child,
pubmed-meshheading:2210975-Consanguinity,
pubmed-meshheading:2210975-Humans,
pubmed-meshheading:2210975-Hyperoxaluria, Primary,
pubmed-meshheading:2210975-Male,
pubmed-meshheading:2210975-Pedigree,
pubmed-meshheading:2210975-Urinary Calculi
|
| pubmed:year |
1990
|
| pubmed:articleTitle |
Early onset of stone diseases and primary hyperoxaluria.
|
| pubmed:affiliation |
Department of Paediatric Nephrology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|