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Primary hyperoxaluria (glycolic acid variant): a clinical and genetical investigation of eight cases.
1978 (English)In: Upsala Journal of Medical Sciences, ISSN 0300-9734, E-ISSN 2000-1967, Vol. 83, no 1, p. 65-70Article in journal (Refereed) Published
Abstract [en]

The clinical features of eight cases of primary hyperoxaluria have been summarized. The possibility of different phenotypes is discussed. A reduction, but no normalization, of the oxalate formation during pyridoxine therapy was found. A renal transplantation performed in one of the patients failed because of the formation of nephrocalcinosis.

Place, publisher, year, edition, pages
1978. Vol. 83, no 1, p. 65-70
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URN: urn:nbn:se:hv:diva-13315PubMedID: 705974OAI: oai:DiVA.org:hv-13315DiVA, id: diva2:1273791
Note

Professor Gösta Samuelson samlade trycksaker; 55

Available from: 2018-12-21 Created: 2018-12-21 Last updated: 2019-08-20Bibliographically approved

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