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Mineral and Electrolyte Metabolism|January 1, 1997
Hyperhomocysteinemia is associated with atherosclerotic occlusive arterial accidents in predialysis chronic renal failure patientsP Jungers, P Chauveau, O Bandin, et al.
Prenatal Diagnosis|July 6, 2006
Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experienceB Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Prenatal Diagnosis|December 2, 2009
Gestational age-related reference values for amniotic fluid organic acidsC Ottolenghi, N Abermil, A Lescoat, et al.
The Journal of Pediatrics|August 1, 1992
Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosisJ P Bonnefont, D Chretien, P Rustin, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?L Thuillier, B Chadefaux-Vekemans, J P Bonnefont, et al.
Neuromuscular Disorders : NMD|March 29, 2000
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patientL Thuillier, C Sevin, F Demaugre, et al.
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