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Annales De Biologie Clinique|January 1, 1977
[Hyperglycinemia without ketosis. Biochemical and enzymatic study]N Dingeon, M O Rolland, P Divry, et al.
Archives Francaises De Pediatrie|May 1, 1979
[Glutaric aciduria. 1 new case]D Floret, P Divry, N Dingeon, et al.
Biomedical & Environmental Mass Spectrometry|November 1, 1987
Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year periodP Divry, C Vianey-Liaud, J Cotte
Journal of Inherited Metabolic Disease|January 1, 1984
Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiencyP Divry, C Vianey-Liaud, J Cotte
Nephrologie|January 1, 1994
[Molecular pathology of type 1 primary hyperoxaluria]P Cochat, M O Rolland, D Bozon, et al.
Pediatric Neurology|May 1, 1993
Mevalonic aciduria in 3 siblings: a new recognizable metabolic encephalopathyJ Mancini, N Philip, B Chabrol, et al.
European Journal of Pediatrics|May 1, 1981
Serum orosomucoid concentration in newborn infantsL Sann, J Bienvenu, C Lahet, 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.
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