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Acta Paediatrica Scandinavica|November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhoodP Divry, M David, N Gregersen, 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.Pediatrie|January 1, 1992
[Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia]C Elleau, F Parrot-Roulaud, Y Perel, et al.Journal of Inherited Metabolic Disease|January 1, 1993
Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): comparison of enzymatic and metabolite analysisM J Bennett, K M Gibson, W G Sherwood, 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.American Journal of Human Genetics|July 27, 1999
Identification of a mutation cluster in mevalonate kinase deficiency, including a new mutation in a patient of Mennonite ancestryD D Hinson, R M Ross, S Krisans, et al.The Biochemical Journal|April 15, 1997
A nonsense mutation in the 3-hydroxy-3-methylglutaryl-CoA lyase gene produces exon skipping in two patients of different origin with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyJ Pié, N Casals, C H Casale, et al.Annales De Biologie Clinique|January 1, 1988
[Biological diagnosis of hereditary metabolic diseases. From selective screening to the mutant-cell bank]P Divry, I Maire, M MathieuPathologie-Biologie|June 1, 1975
[Determination of glomerular and tubular clearance in children without urine collection]N Dingeon, C Collombel, C Artru, et al.Annales De Biologie Clinique|January 1, 1991
[Inborn errors of lysine metabolism]P Divry, C Vianey-Liaud, M MathieuPageof 14