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Clinical Biochemistry|August 1, 1991
Detection of hereditary metabolic disorders involving amino acids and organic acidsV E ShihClinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1978
Plasma and urine amino acid changes in rats treated with hypoglycinV E Shih, K TanakaThe American Review of Respiratory Disease|July 1, 1983
Relationship between central nervous system hydrogen ion regulation and amino acid metabolism in hypercapniaB Hoop, V E Shih, H KazemiMolecular Genetics and Metabolism|July 29, 2009
Argininosuccinate lyase deficiency: longterm outcome of 13 patients detected by newborn screeningC Ficicioglu, R Mandell, V E ShihThe Journal of Clinical Investigation|July 1, 1976
Metabolism of [1-(14)C] and [2-(14)C] leucine in cultured skin fibroblasts from patients with isovaleric acidemia. Characterization of metabolic defectsK Tanaka, R Mandell, V E ShihThe American Review of Respiratory Disease|August 1, 1985
Relationship between central nervous system hydrogen ion regulation and amino acid metabolism in hypercapnia, IIB Hoop, V E Shih, H KazemiClinica Chimica Acta; International Journal of Clinical Chemistry|February 5, 1982
Defective ornithine metabolism in cultured skin fibroblasts from patients with the syndrome of hyperornithinemia, hyperammonemia and homocitrullinuriaV E Shih, R Mandell, A HerzfeldAmerican Journal of Human Genetics|December 1, 1988
Pyridoxine effects on ornithine ketoacid transaminase activity in fibroblasts from carriers of two forms of gyrate atrophy of the choroid and retinaV E Shih, R Mandell, E L BersonClinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1981
Reduction of hyperornithinemia with a low protein, low arginine diet and pyridoxine in patients with a deficiency of ornithine-ketoacid transaminase (OKT) activity and gyrate atrophy of the choroid and retinaV E Shih, E L Berson, M GargiuloPageof 7