Showing results (31-40 of 199) with videos related to
Sort By:
Pageof 20
Biochemical Medicine|June 1, 1983
Effect of experimental hyperphenylalaninemia on biogenic amine synthesis at later stages of brain developmentE H Taylor, F A Hommes, D E StewartHelvetica Paediatrica Acta|July 1, 1980
[Chronic infantile lactate acidosis]D Papanastasiou, W Lehnert, L Schuchmann, et al.Journal of Inherited Metabolic Disease|January 1, 1982
Turnover of the fast components of myelin and myelin proteins in experimental hyperphenylalaninaemia. Relevance to termination of dietary treatment in human phenylketonuriaF A Hommes, A G Eller, E H TaylorClinica Chimica Acta; International Journal of Clinical Chemistry|April 15, 1986
HPLC assay of phenylalanine and tyrosine in blood spots on filter paperR A Roesel, P R Blankenship, F A HommesNutrition and Metabolism|January 1, 1975
The effect of vitamin E deficiency on permeability of mitochondria for phosphateF A Hommes, D J Mastebroek-Helder, I MolenaarActa Paediatrica Scandinavica|January 1, 1976
A case of methylmalonic and propionic acidemia due to methulmalonyl-CoA carbonylmutase apoenzyme deficiencyH van den Berg, M T Boelkens, F A HommesJournal of Medical Genetics|June 1, 1992
An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosisB Say, F A Hommes, S A Malik, et al.Helvetica Paediatrica Acta|October 1, 1975
Studies on the valine sensitivity in non-ketotic hyperglycinemiaC J de Groot, H van den Berg, F A HommesJournal of Inherited Metabolic Disease|January 1, 1986
Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactorR A Roesel, F Bowyer, P R Blankenship, et al.Journal of Inherited Metabolic Disease|January 1, 1991
N-acetylglutamate synthetase deficiency: clinical and laboratory observationsA L Pandya, R Koch, F A Hommes, et al.Pageof 20