Primary hyperoxaluria Type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort-Reference-Cited by-同舟云学术

Primary hyperoxaluria Type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort

Published:2012-07-27 Issue:10 Volume:27 Page:3855-3862
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

van der Hoeven S. M.,van Woerden C. S.,Groothoff J. W.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/27/10/3855/6879938/gfs320.pdf

Reference24 articles.

1. PEROXISOMAL ALANINE:GLYOXYLATE AMINOTRANSFERASE AND PRENATAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1

2. Molecular Etiology of Primary Hyperoxaluria Type 1: New Directions for Treatment

3. The primary hyperoxalurias

4. Cardiac Abnormalities in Primary Hyperoxaluria

5. Molecular Aetiology of Primary Hyperoxaluria Type 1

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