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Journal of Inherited Metabolic Disease|January 1, 1981
Renal transport of aromatic acids in patients with phenylketonuriaU Langenbeck, A Behbehani, H LutheJournal of Inherited Metabolic Disease|January 1, 1980
Argininosuccinic acid synthetase deficiency in a hamster cell line and its complementation of argininosuccinic aciduria human fibroblastsA González-Noriega, J Verduzco, E Prieto, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Mild variant of argininosuccinic aciduriaR B Schutgens, F A Beemer, W H Tegelaers, et al.Journal of Inherited Metabolic Disease|January 1, 1982
Normal 2-aminobutyrate oxidation and increased valine oxidation in fibroblasts deficient in pyruvate dehydrogenaseO Borud, J E PettersenJournal of Inherited Metabolic Disease|January 1, 1982
Cerebrotendinous xanthomatosis: a defect in cellular sterol biosynthetic controlJ L Barron, J U Maxwell, G S RutherfoordJournal of Inherited Metabolic Disease|January 1, 1982
Effects of Econazole, Fungizone and Pimafucin on cell growth, lysosomal enzyme activity and sulphate metabolism of cultured human skin fibroblasts and amniotic fluid cellsJ ButterworthJournal of Inherited Metabolic Disease|January 1, 1982
Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiencyL Caimi, G Tettamanti, B Berra, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Genetic heterogeneity of membrane-bound beta-glucosidase in Gaucher's diseaseM CarrollJournal of Inherited Metabolic Disease|January 1, 1980
Prenatal diagnosis of I-cell disease by measuring altered alpha-mannosidase activity in amniotic fluidM Owada, O Nishiya, T Sakiyama, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Uptake of lysosomal enzymes by human fibroblasts: lack of uptake of fungal or plant glycosidases in comparison with a mammalian enzymeK C Dooley, D A ApplegarthPageof 429