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F A Hommes

Showing results (71-80 of 104) with videos related to

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Acta 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 Hommes
Journal 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 Hommes
Journal 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.
Journal of Inherited Metabolic Disease|January 1, 1984
Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndromeK Metoki, F A Hommes, P Dyken, et al.
Annals of the New York Academy of Sciences|December 18, 1972
Mitochondrial and microsomal membranes from livers of vitamin E-deficient ducklingsJ Vos, I Molenaar, M Searle-van Leeuwen, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|February 1, 1979
2,3-Dihydroxybutane: an unusual compound found in the gaschromatographic analysis of volatile compounds of urineF A Hommes, A P Bruins, J Dajani-Wielaard, et al.
Enzyme|January 1, 1976
The development of creatine kinase in rat skeletal muscle. Changes in isoenzyme ratio, protein, RNA and DNA during developmentH J Kloosterboer, S A Stoker-de Vries, F A Hommes
FEBS Letters|May 7, 1984
Reconstitution of ornithine transport in liposomes with Lubrol extracts of mitochondriaF A Hommes, A G Eller, B A Evans, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Acta 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 Hommes
Journal 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 Hommes
Journal 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.
Journal of Inherited Metabolic Disease|January 1, 1984
Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndromeK Metoki, F A Hommes, P Dyken, et al.
Annals of the New York Academy of Sciences|December 18, 1972
Mitochondrial and microsomal membranes from livers of vitamin E-deficient ducklingsJ Vos, I Molenaar, M Searle-van Leeuwen, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|February 1, 1979
2,3-Dihydroxybutane: an unusual compound found in the gaschromatographic analysis of volatile compounds of urineF A Hommes, A P Bruins, J Dajani-Wielaard, et al.
Enzyme|January 1, 1976
The development of creatine kinase in rat skeletal muscle. Changes in isoenzyme ratio, protein, RNA and DNA during developmentH J Kloosterboer, S A Stoker-de Vries, F A Hommes
FEBS Letters|May 7, 1984
Reconstitution of ornithine transport in liposomes with Lubrol extracts of mitochondriaF A Hommes, A G Eller, B A Evans, et al.
Pageof 11