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Nephrologie|January 1, 1994
[Molecular pathology of type 1 primary hyperoxaluria]P Cochat, M O Rolland, D Bozon, et al.Human Mutation|June 22, 2000
Identification of 5 novel mutations in the AGXT geneO Basmaison, M O Rolland, P Cochat, et al.European Journal of Pediatrics|December 22, 1999
Combined liver-kidney transplantation in primary hyperoxaluria type 1P Cochat, J M Gaulier, P C Koch Nogueira, et al.Human Mutation|March 29, 2000
Partial deletion of the AGXT gene (EX1_EX7del): A new genotype in hyperoxaluria type 1P K Nogueira, T S Vuong, O Bouton, et al.Annales De Biologie Clinique|January 1, 1977
[Hyperglycinemia without ketosis. Biochemical and enzymatic study]N Dingeon, M O Rolland, P Divry, et al.La Revue Du Praticien|November 20, 1997
[Hereditary diseases causing kidney calculi]P Cochat, M Jouvenet, H Pellet, et al.Pediatric Neurology|May 1, 1993
Mevalonic aciduria in 3 siblings: a new recognizable metabolic encephalopathyJ Mancini, N Philip, B Chabrol, et al.Pediatrie|January 1, 1989
[Biotidinase deficiency: a disease with neurologic and cutaneous expression susceptible to biotin]L de Parscau, B Beaufrère, C Vianey-Liaud, et al.The Journal of Pediatrics|December 10, 1999
Primary hyperoxaluria in infants: medical, ethical, and economic issuesP Cochat, P C Koch Nogueira, M A Mahmoud, et al.Archives of Biochemistry and Biophysics|October 24, 1998
Two missense point mutations in different alleles in the 3-hydroxy-3-methylglutaryl coenzyme A lyase gene produce 3-hydroxy-3-methylglutaric aciduria in a French patientN Zapater, J Pié, J Lloberas, et al.Pageof 30