Les formes infantiles de l'hyperoxalurie primaire de type I: à propos de quatre cas
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference11 articles.
1. Enzymological diagnosis of primary hyperoaluria type I by measurement of hepatic alanine: glyoxylate aminotransferase activity;Danpure;Lancet,1987
2. Characteristization and chromosomal mapping of a genomic clone encoding human alanin: glyoxylate aminotransferase;Purdue;Genomics,1991
3. Primarily hyperoxalurias;Hillman,1989
4. Oxalosis in infancy;Morris;Arch Dis Child,1982
5. Molecular and clinical heterogeneity in primary hyperoxaluria I;Danpure;Am J Kidney Dis,1991
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Primary hyperoxaluria in a compound heterozygote infant;World Journal of Pediatrics;2010-06-12
2. Localisation digestive exceptionnelle des dépôts cristallins dans l’hyperoxalurie primitive;Archives de Pédiatrie;2009-11
3. Primary hyperoxaluria in infants: Medical, ethical, and economic issues;The Journal of Pediatrics;1999-12
4. Primary Hyperoxaluria Type I: An Underestimated Cause of Nephrocalcinosis and Chronic Renal Failure in Saudi Arabian Children;Annals of Saudi Medicine;1999-01
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