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Annals of Neurology|November 1, 1991
Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeC A Stanley, S DeLeeuw, P M Coates, et al.
Journal De Genetique Humaine|January 1, 1988
[Genetic heterogeneity of cystinuria. Study of 12 families]J Nissiotou, C Vianey-Liaud, B Parchoux, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samplesJ M Parnet, P Divry, C Vianey-Saban, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblastsC Bertrand, R Dumoulin, P Divry, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1987
Hemoglobin J-Baltimore (beta 16(A13)Gly----Asp): interference with the assay of HbA1cF Vandenesch, F Baklouti, A Francina, et al.
American Journal of Obstetrics and Gynecology|October 1, 1990
Antenatal diagnosis of molybdenum cofactor deficiencyR G Gray, A Green, S N Basu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 14, 1998
Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patientsC Vianey-Saban, P Divry, M Brivet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 1997
[Study of plasma acylcarnitines using tandem mass spectrometry. Application to the diagnosis of metabolism hereditary diseases]F Delolme, C Vianey-Saban, N Guffon, et al.
European Journal of Pediatrics|April 1, 1993
Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemiaC Vianey-Saban, B Mousson, C Bertrand, et al.
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