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Annales De Biologie Clinique|January 1, 1991
[Inborn errors of lysine metabolism]P Divry, C Vianey-Liaud, M MathieuJournal of Inherited Metabolic Disease|January 1, 1987
The inborn errors of mitochondrial fatty acid oxidationC Vianey-Liaud, P Divry, N Gregersen, et al.Annales De Biologie Clinique|January 1, 1991
[Lysine metabolism in man]C Vianey-Liaud, P Divry, C Poinas, 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 CotteJournal 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 CotteNeuropediatrics|May 1, 1989
Spongy degeneration of the neuraxis (Canavan-van Bogaert disease) and N-acetylaspartic aciduriaB Echenne, P Divry, C Vianey-LiaudArchives Francaises De Pediatrie|December 1, 1988
[Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline]L de Parscau, C Vianey-Liaud, M Hermier, et al.Pathologie-Biologie|April 1, 1986
[Determination of serum proline iminopeptidase activity using a fluorescent substrate in patients with Paget's disease and prostatic bone metastases. Preliminary results]M Bouvier, F Colson, J Tebib, 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.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 MathieuPageof 37