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Journal of Inherited Metabolic Disease|January 1, 1993
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new caseN Guffon, C Lopez-Mediavilla, R Dumoulin, et al.Acta Paediatrica Scandinavica|November 1, 1982
Effect of oral lipid administration on glucose homeostasis in small-for-gestational-age infantsL Sann, P Divry, Y Lasne, et al.Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire|April 1, 1977
[Painful and transient spasm of the cardioesophageal sphincter (author's transl)]C Tavernier, P Divry, A Delfolie, et al.Archives Francaises De Pediatrie|June 1, 1991
[N-acetylaspartic aciduria. Clinical, biological and physiopathological study]C Gay, P Divry, V Macabeo, et al.Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire|December 1, 1975
[Intravenous duodenography: a routine investigation (author's transl)]C Tavernier, P Divry, A Delafolie, et al.Archives Francaises De Pediatrie|May 1, 1979
[Glutaric aciduria. 1 new case]D Floret, P Divry, N Dingeon, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1984
Hypoxanthine and xanthine concentrations determined by high performance liquid chromatography in biological fluids from patients with xanthinuriaR Boulieu, C Bory, P Baltassat, 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.Annals of Neurology|January 1, 1993
3-Methylglutaconic aciduria in "optic atrophy plus"H Costeff, O Elpeleg, N Apter, et al.Nephrologie|January 1, 1994
[Molecular pathology of type 1 primary hyperoxaluria]P Cochat, M O Rolland, D Bozon, et al.Pageof 37