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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 Luthe
Journal 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 Pettersen
Journal of Inherited Metabolic Disease|January 1, 1982
Cerebrotendinous xanthomatosis: a defect in cellular sterol biosynthetic controlJ L Barron, J U Maxwell, G S Rutherfoord
Journal 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 Carroll
Journal 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.
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