Author:
Belhaj R.,Hayder N.,Gargueh T.,Zorguati M.,Marrakchi O.,Abdelhak S.,Lakhoua R.,Abdelmoula J.
Reference19 articles.
1. Peroxisomial alanine–glyoxalate aminotransferase deficiency in primary hperoxaluria type 1;Danpure;Lancet,1986
2. Hyperoxaluries massives;Barbey;Rev Med Suisse Romande,2004
3. Worldwide view of infantile primary hyperoxaluria type 1 (PH1);Cochat;Nephrol Dial Transplant,1999
4. Primary hyperoxaluria type 1: a model for multiple mutations in a monogenic disease within a distinct ethnic group;Rinat;J Am Soc Nephrol,1999
5. Hyperoxalurie primitive chez l’enfant au centre tunisien;Chemli;Tunis Med,2003
Cited by
12 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