z-logo
open-access-imgOpen Access
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom