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Clinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1979
Urinary dihydroxanthopterin in the diagnosis of malignant hyperphenylalaninemia and phenylketonuriaP Schlesinger, B M Watson, R G Cotton, et al.Pediatric Research|October 1, 1979
Malignant hyperphenylalaninemia--clinical features, biochemical findings, and experience with administration of biopterinsD M Danks, P Schlesinger, F Firgaira, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 2, 1979
Human dihydropteridine reductase: a method for the measurement of activity in cultured cells, and its application to malignant hyperphenylalaninemiaF A Firgaira, R G Cotton, D M DanksJournal of Inherited Metabolic Disease|January 1, 1985
Liver enzyme activities in hyperphenylalaninaemia due to a defective synthesis of tetrahydrobiopterinJ L Dhondt, R G Cotton, D M DanksLancet (London, England)|December 15, 1979
Dihydropteridine reductase deficiency diagnosis by assays on peripheral blood-cellsF A Firgaira, R G Cotton, D M DanksThe Biochemical Journal|July 1, 1981
Isolation and characterization of dihydropteridine reductase from human liverF A Firgaira, R G Cotton, D M DanksThe Journal of Pediatrics|October 1, 1977
Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiencyL J Sheffield, P Schlesinger, K Faull, et al.Journal of Medical Genetics|January 1, 1988
The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiencyH H Dahl, S Wake, R G Cotton, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Two-dimensional polyacrylamide gel analysis of fibroblast polypeptides: discussion of its relevance for inherited diseasesK H Choo, R G Cotton, D M Danks, et al.Pageof 29