L Sweetman|W L Nyhan - JoVE Visualize

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Journal of Neurogenetics|December 1, 1985

Metabolism of leucine in fibroblasts from patients with deficiencies in each of the major catabolic enzymes: branched-chain ketoacid dehydrogenase, isovaleryl-CoA dehydrogenase, 3-methylcrotonyl-CoA carboxylase, 3-methylglutaconyl-CoA hydratase, and 3-hydroxy-3-methylglutaryl-CoA lyaseI Yoshida, O Søvik, L Sweetman, et al.

Pediatric Research|August 1, 1984

Stable isotope dilution analysis of galactitol in amniotic fluid: an accurate approach to the prenatal diagnosis of galactosemiaC Jakobs, T G Warner, L Sweetman, et al.

Journal of Neurogenetics|September 1, 1984

Succinic semialdehyde dehydrogenase deficiencyK M Gibson, L Sweetman, W L Nyhan, et al.

American Journal of Human Genetics|July 1, 1984

Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblastsO Sovik, L Sweetman, K M Gibson, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1989

3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detectionK Narisawa, K M Gibson, L Sweetman, et al.

Pediatric Research|November 1, 1977

Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuriaL Sweetman, S P Bates, D Hull, et al.

Journal of Inherited Metabolic Disease|January 1, 1985

Demonstration of 4-aminobutyric acid aminotransferase deficiency in lymphocytes and lymphoblastsK M Gibson, L Sweetman, W L Nyhan, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 1977

Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuriaW Weyler, L Sweetman, D C Maggio, et al.

Annals of Neurology|September 1, 1977

Biochemical correlates of illness and recovery in Reye's syndromeD Trauner, L Sweetman, J Holm, et al.

Pediatric Research|December 1, 1979

Utilization of purines by an HPRT variant in an intelligent, nonmutilative patient with features of the Lesch-Nyhan syndromeB Bakay, E Nissinen, L Sweetman, et al.

Pageof 26

Showing results (11-20 of 255) with videos related to

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Pageof 26

Journal of Neurogenetics|December 1, 1985

Metabolism of leucine in fibroblasts from patients with deficiencies in each of the major catabolic enzymes: branched-chain ketoacid dehydrogenase, isovaleryl-CoA dehydrogenase, 3-methylcrotonyl-CoA carboxylase, 3-methylglutaconyl-CoA hydratase, and 3-hydroxy-3-methylglutaryl-CoA lyaseI Yoshida, O Søvik, L Sweetman, et al.

Pediatric Research|August 1, 1984

Stable isotope dilution analysis of galactitol in amniotic fluid: an accurate approach to the prenatal diagnosis of galactosemiaC Jakobs, T G Warner, L Sweetman, et al.

Journal of Neurogenetics|September 1, 1984

Succinic semialdehyde dehydrogenase deficiencyK M Gibson, L Sweetman, W L Nyhan, et al.

American Journal of Human Genetics|July 1, 1984

Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblastsO Sovik, L Sweetman, K M Gibson, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1989

3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detectionK Narisawa, K M Gibson, L Sweetman, et al.

Pediatric Research|November 1, 1977

Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuriaL Sweetman, S P Bates, D Hull, et al.

Journal of Inherited Metabolic Disease|January 1, 1985

Demonstration of 4-aminobutyric acid aminotransferase deficiency in lymphocytes and lymphoblastsK M Gibson, L Sweetman, W L Nyhan, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 1977

Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuriaW Weyler, L Sweetman, D C Maggio, et al.

Annals of Neurology|September 1, 1977

Biochemical correlates of illness and recovery in Reye's syndromeD Trauner, L Sweetman, J Holm, et al.

Pediatric Research|December 1, 1979

Utilization of purines by an HPRT variant in an intelligent, nonmutilative patient with features of the Lesch-Nyhan syndromeB Bakay, E Nissinen, L Sweetman, et al.

Pageof 26