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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.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 HommesFEBS 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.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 16, 1984
Gamma-glutamylornithine excretion in patients with hyperornithinemiaR A Roesel, M E Coryell, P R Blankenship, et al.Journal of Inherited Metabolic Disease|January 1, 1985
Biochemical observations on a case of hepatic fructose-1,6-diphosphatase deficiencyF A Hommes, R Campbell, C Steinhart, et al.Neurology|September 1, 1986
Anticonvulsive drugs and blood levels of lactate, pyruvate, and glucose in children with seizuresA L Carter, P L Hartlage, A G Eller, et al.The Journal of Reproductive Medicine|February 1, 1988
Activity of arylsulfatase A, B-glucosidase and hexosaminidases in chorionic villi at six, eight and ten weeks' gestational ageJ V Johnson, F A Hommes, P G McDonough, et al.Pageof 7