Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome
Author(s) -
Christiaan S. van Woerden
Publication year - 2003
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/18.2.273
Subject(s) - medicine , nephrocalcinosis , primary hyperoxaluria , pediatrics , incidence (geometry) , renal function , cohort , kidney disease , surgery , kidney , physics , optics
Primary hyperoxaluria type 1 (PH1) is a phenotypically heterogeneous disease. To date the relationship between biochemical parameters and outcome is unclear. We therefore undertook a national cohort study on biochemical and clinical parameters and outcome in PH1.
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