Immediate commencement of amino acid supplementation in preterm infants: Effect on serum amino acid concentrations and protein kinetics on the first day of life von Van Goudoever, J.B., Colen, T., Wattimena, J.L.D., Huijmans, J.G.M., Carnielli, V.P., Sauer, P.J.J.

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Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib) von Schollen, E., Dorland, L., de Koning, T.J., Van Diggelen, O.P., Huijmans, J.G.M., Marquardt, T., Babovic-Vuksanovic, D., Patterson, M., Imtiaz, F., Winchester, B., Adamowicz, M., Pronicka, E., Freeze, H., Matthijs, G.

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Juvenile Hyaline Fibromatosis: Clinical Heterogeneity in Three Patients von Mancini, G.M.S., Stojanov, L., Willemsen, R., Kleijer, W.J., Huijmans, J.G.M., van Diggelen, O.P., de Klerk, J.B.C., Vuzevski, V.D., Oranje, A.P.

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Amino Acid Solutions for Premature Neonates During the First Week of Life: The Role of N-Acetyl-L-Cysteine and N-Acetyl-L-Tyrosine von Van Goudoever, J.B., Sulkers, E.J., Timmerman, M., Huijmans, J.G.M., Langer, K., Carnielli, V.P., Sauer, P.J.J.

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Albumin and whole-body protein synthesis respond differently to intraperitoneal and oral amino acids von Tjiong, H.L., Fieren, M.W., Rietveld, T., Wattimena, J.L., Schierbeek, H., Huijmans, J.G.M., Hop, W.C., Swart, G.R., van den Berg, J.W.

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Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency von de Wit, M.C.Y., de Coo, I.F.M., Verbeek, E., Schot, R., Schoonderwoerd, G.C., Duran, M., de Klerk, J.B.C., Huijmans, J.G.M., Lequin, M.H., Verheijen, F.W., Mancini, G.M.S.

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Peritoneal Protein Losses and Cytokine Generation in Automated Peritoneal Dialysis with Combined Amino Acids and Glucose Solutions von TJIONG, H. L, ZIJLSTRA, F. J, RIETVELD, T, WATTIMENA, J. L, HUIJMANS, J. G. M, SWART, G. R, FIEREN, M. W. J. A

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L‐2‐Hydroxyglutaric aciduria: Normal L‐2‐hydroxyglutarate dehydrogenase activity in liver from two new patients von Wanders, R.J.A., Vilarinho, L., Hartung, H.P., Hoffmann, G.F., Mooijer, P.A.W., Jansen, G.A., Huijmans, J.G.M., Klerk, J.B.C., Brink, H.J., Jakobs, C., Duran, M.

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4124 Identification of glycosaminoglycans in age-related macular deposits von Kliffen, M., Huijmans, J.G.M., Mooy, C.M., Luider, T.M., Kerkvliet, S., De Jong, P.T.V.M.

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SUCCESSFUL TREATMENT OF INFANTILE TYPE I PRIMARY HYPEROXALURIA COMPLICATED BY PYRIDOXINE TOXICITY von De Zegher, F., Przyrembel, H., Chalmers, R.A., Wolff, E.D., Huijmans, J.G.M.

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Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease) von Blom, W., Luteyn, J.C., Kelholt-Dijkman, H.H., Huijmans, J.G.M., Loonen, M.C.B.

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Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome von Wanders, R.J.A., Van Roermund, C.W.T., Westra, R., Schutgens, R.B.H., van der Ende, M.A., Tager, J.M., Monnens, L.A.H., Baadenhuysen, H., Govaerts, L., Przyrembel, H., Wolff, E.D., Blom, W., Huijmans, J.G.M., van Laerhoven, F.G.M.

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Defects in Mitochondrial Beta Oxidationa von SCHOLTE, H.R., LUYT‐HOUWEN, I.E.M., BLOM, W., BUSCH, H.F.M., JONGE, P.C., VISSER, M., HUIJMANS, J.G.M., JENNEKENS, F.G.I., MOOY, P.D., PRZYREMBEL, H., SCHUTGENS, R.B.H., VAANDRAGER‐VERDUIN, M.H.M., COSTER, R.N.A.

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Defects in Mitochondrial Beta Oxidation von SCHOLTE, H.R., LUYT-HOUWEN, I.E.M., BLOM, W., BUSCH, H.F.M., JONGE, P.C., VISSER, M., HUIJMANS, J.G.M., JENNEKENS, F.G.I., MOOY, P.D., PRZYREMBEL, H., SCHUTGENS, R.B.H., VAANDRAGER-VERDUIN, M.H.M., COSTER, R.N.A.

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Defects in Mitochondrial Beta Oxidation von SCHOLTE, H.R., LUYT-HOUWEN, I.E.M., BLOM, W., BUSCH, H.F.M., DE JONGE, P.C., DE VISSER, M., HUIJMANS, J.G.M., JENNEKENS, F.G.I., MOOY, P.D., PRZYREMBEL, H., SCHUTGENS, R.B.H., VAANDRAGER-VERDUIN, M.H.M., VAN COSTER, R.N.A.

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Different effects of cycloheximide and chloramphenicol on corticosterone production by isolated rat adrenal cells von Falke, H.E., Huijmans, J.G.M., Degenhart, H.J.

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