Authors: GALVINPARTON P HOMMES FA

Citation: P. Galvinparton et Fa. Hommes, ABNORMAL OLIGOSACCHARIDE PATTERN IN GLYCOGEN-STORAGE-DISEASE TYPE-III, Journal of inherited metabolic disease, 19(3), 1996, pp. 383-384

Authors: ARTHUR K HOMMES FA

Citation: K. Arthur et Fa. Hommes, SIMPLE ISOTOPE-DILUTION ASSAY FOR PROPIONIC-ACID AND ISOVALERIC ACID, Journal of chromatography B. Biomedical applications, 673(1), 1995, pp. 132-135

Authors: HOMMES FA

Citation: Fa. Hommes, LOSS OF NEUROTRANSMITTER RECEPTORS BY HYPERPHENYLALANINEMIA IN THE HPH-5 MOUSE-BRAIN, Acta paediatrica, 83, 1994, pp. 120-121

Authors: HOMMES FA

Citation: Fa. Hommes, QUALITY-CONTROL FOR SELECTIVE SCREENING OF INBORN-ERRORS OF METABOLISM, European journal of pediatrics, 153(7), 1994, pp. 190000017-190000022

Authors: HOMMES FA

Citation: Fa. Hommes, THE EFFECT OF HYPERPHENYLALANINEMIA ON THE MUSCARINIC ACETYLCHOLINE-RECEPTOR IN THE HPH-5 MOUSE-BRAIN, Journal of inherited metabolic disease, 16(6), 1993, pp. 962-974

Authors: HOMMES FA

Citation: Fa. Hommes, INBORN-ERRORS OF FRUCTOSE METABOLISM, The American journal of clinical nutrition, 58(5), 1993, pp. 190000788-190000795