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Journal of Inherited Metabolic Disease|January 1, 1980
Beta-glucuronidase deficiency: enzyme studies in an affected family and prenatal diagnosisI Maire, G Mandon, M T Zabot, et al.Archives of Disease in Childhood|May 1, 1984
Severe ornithine transcarbamylase deficiency. Two and a half years' survival with normal developmentP Guibaud, P Baxter, J Bourgeois, et al.Journal De Genetique Humaine|June 1, 1983
[Case of mucolipidosis type I with a primary alpha-D-neuraminidase deficiency]J J Louis, I Maire, M Hermier, et al.The Journal of Biological Chemistry|October 21, 1994
The rabbit kidney tubule utilizes glucose for glutamine synthesis. A 13C NMR studyM F Chauvin, F Mégnin-Chanet, G Martin, et al.La Revue Du Praticien|November 20, 1997
[Hereditary diseases causing kidney calculi]P Cochat, M Jouvenet, H Pellet, et al.Pediatrie|January 1, 1991
[Organization of organ transplantation in France]J J Colpart, D Noury, P Cochat, et al.Pediatric Transplantation|May 21, 2003
Quality of life of children and adolescents after kidney or liver transplantation: child, parents and caregiver's point of viewS Manificat, A Dazord, P Cochat, et al.Pediatrie|January 1, 1986
[Anatomical study of the kidneys of newborn infants dying after a septic state]P Cochat, J Bourgeois, J Gilly, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Epidemiology of primary hyperoxaluria type 1. Société de Néphrologie and the Société de Néphrologie PédiatriqueP Cochat, A Deloraine, M Rotily, et al.Archives Francaises De Pediatrie|January 1, 1993
[Subglottal stenosis following intubation in children]D Stamm, D Floret, C Stamm, et al.Pageof 32