Peritoneal Protein Losses and Cytokine Generation in Automated Peritoneal Dialysis with Combined Amino Acids and Glucose Solutions
TJIONG, H. L, ZIJLSTRA, F. J, RIETVELD, T, WATTIMENA, J. L, HUIJMANS, J. G. M, SWART, G. R, FIEREN, M. W. J. A
Published in Mediators of Inflammation (01.01.2007)
Published in Mediators of Inflammation (01.01.2007)
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Albumin and whole-body protein synthesis respond differently to intraperitoneal and oral amino acids
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.
Published in Kidney international (01.08.2007)
Published in Kidney international (01.08.2007)
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Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families
Kleijer, W. J., Garritsen, V. H., Linnebank, M., Mooyer, P., Huijmans, J. G. M., Mustonen, A., Simola, K. O. J., Arslan‐Kirchner, M., Battini, R., Briones, P., Cardo, E., Mandel, H., Tschiedel, E., Wanders, R. J. A., Koch, H. G.
Published in Journal of inherited metabolic disease (01.09.2002)
Published in Journal of inherited metabolic disease (01.09.2002)
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The Role of Nitric Oxide in Bacterial Meningitis in Children
Kornelisse, R. F., Hoekman, K., Visser, J. J., Hop, W. C. J., Huijmans, J. G. M., van der Straaten, P. J. C., van der Heijden, A. J., Sukhai, R. N., Neijens, H. J., de Groot, R.
Published in The Journal of infectious diseases (01.07.1996)
Published in The Journal of infectious diseases (01.07.1996)
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Fatal neonatal malonic aciduria
Buyukgebiz, B., Jakobs, C., Scholte, H.R., Huijmans, J. G. M., Kleijer, W. J.
Published in Journal of inherited metabolic disease (01.02.1998)
Published in Journal of inherited metabolic disease (01.02.1998)
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Glycogen storage disease type III with diagnosis complicated by gluten‐sensitive enteropathy
Artan, R., Diggelen, O. P., Huijmans, J. G. M.
Published in Journal of inherited metabolic disease (01.06.1998)
Published in Journal of inherited metabolic disease (01.06.1998)
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Sudden infant death and lysinuric protein intolerance
de Klerk, J B, Duran, M, Huijmans, J G, Mancini, G M
Published in European journal of pediatrics (01.03.1996)
Published in European journal of pediatrics (01.03.1996)
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PRENATAL DIAGNOSIS OF SANFILIPPO A SYNDROME: EXPERIENCE IN 35 PREGNANCIES AT RISK AND THE USE OF A NEW FLUOROGENIC SUBSTRATE FOR THE HEPARIN SULPHAMIDASE ASSAY
KLEIJER, W. J., KARPOVA, E. A., GEILEN, G. C., KEULEMANS, J. L. M., HUIJMANS, J. G. M., TSVETKOVA, I. V., VOZNYI, YA. V., VAN DIGGELEN, O. P.
Published in Prenatal diagnosis (01.09.1996)
Published in Prenatal diagnosis (01.09.1996)
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Prenatal diagnosis of the urea cycle diseases: a survey of the European cases
Kamoun, P, Fensom, A H, Shin, Y S, Bakker, E, Colombo, J P, Munnich, A, Bird, S, Canini, S, Huijmans, J G, Chadefaux-Vekemans, B
Published in American journal of medical genetics (16.01.1995)
Published in American journal of medical genetics (16.01.1995)
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AMNIOTIC FLUID ODD-CHAIN FATTY ACIDS ARE INCREASED IN PROPIONIC ACIDAEMIA
ÇOKER, M., DURAN, M., DE KLERK, J. B. C., KLEIJER, W. J., JAKOBS, C., HUIJMANS, J. G. M.
Published in Prenatal diagnosis (01.10.1996)
Published in Prenatal diagnosis (01.10.1996)
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Beta-mannosidase deficiency: heterogeneous manifestation in the first female patient and her brother
Kleijer, W J, Hu, P, Thoomes, R, Boer, M, Huijmans, J G, Blom, W, Van Diggelen, O P, Seemanova, E, Macek, M
Published in Journal of inherited metabolic disease (01.01.1990)
Published in Journal of inherited metabolic disease (01.01.1990)
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Prenatal diagnosis of Sanfilippo disease type C using a simple fluorometric enzyme assay
He, W, Voznyi YaV, Huijmans, J G, Geilen, G C, Karpova, E A, Dudukina, T V, Zaremba, J, Van Diggelen, O P, Kleijer, W J
Published in Prenatal diagnosis (01.01.1994)
Published in Prenatal diagnosis (01.01.1994)
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Assessment of deficiencies of fatty acyl-CoA dehydrogenases in fibroblasts, muscle and liver
Scholte, H R, Ross, J D, Blom, W, Boonman, A M, van Diggelen, O P, Hall, C L, Huijmans, J G, Luyt-Houwen, I E, Kleijer, W J, de Klerk, J B
Published in Journal of inherited metabolic disease (01.05.1992)
Published in Journal of inherited metabolic disease (01.05.1992)
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A clinical biochemist's view of the investigation of suspected inherited metabolic disease
Blom, W, Huijmans, J G, van den Berg, G B
Published in Journal of inherited metabolic disease (01.03.1989)
Published in Journal of inherited metabolic disease (01.03.1989)
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beta-Glucuronidase deficiency as a cause of fetal hydrops
Kagie, M J, Kleijer, W J, Huijmans, J G, Maaswinkel-Mooy, P, Kanhai, H H
Published in American journal of medical genetics (01.03.1992)
Published in American journal of medical genetics (01.03.1992)
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The detection of abnormal metabolites in MCAD deficiency: a new method
Blom, W, Polder-Mol, A C, Kelholt-Dijkman, H H, Hierck, L, Huijmans, J G
Published in Journal of inherited metabolic disease (01.05.1990)
Published in Journal of inherited metabolic disease (01.05.1990)
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Effect of 25-hydroxy-cholesterol on the uptake of corticosterone in isolated rat liver cells
Huijmans, J G, Degenharg, H J, Kortleve, D J
Published in Hormone and metabolic research (01.01.1988)
Published in Hormone and metabolic research (01.01.1988)
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