Probing Single-Cell Macrophage Polarization and Heterogeneity Using Thermo-Reversible Hydrogels in Droplet-Based Microfluidics
Tiemeijer, B M, Sweep, M W D, Sleeboom, J J F, Steps, K J, van Sprang, J F, De Almeida, P, Hammink, R, Kouwer, P H J, Smits, A I P M, Tel, J
Published in Frontiers in bioengineering and biotechnology (14.10.2021)
Published in Frontiers in bioengineering and biotechnology (14.10.2021)
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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation
Wanders, R J, IJlst, L, van Gennip, A H, Jakobs, C, de Jager, J P, Dorland, L, van Sprang, F J, Duran, M
Published in Journal of inherited metabolic disease (01.05.1990)
Published in Journal of inherited metabolic disease (01.05.1990)
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3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment
Duran, M, Wanders, R J, de Jager, J P, Dorland, L, Bruinvis, L, Ketting, D, Ijlst, L, van Sprang, F J
Published in European journal of pediatrics (01.01.1991)
Published in European journal of pediatrics (01.01.1991)
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Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis
Jaeken, J, Wadman, S K, Duran, M, van Sprang, F J, Beemer, F A, Holl, R A, Theunissen, P M, de Cock, P, van den Bergh, F, Vincent, M F
Published in European journal of pediatrics (01.11.1988)
Published in European journal of pediatrics (01.11.1988)
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Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method : the effect of oral riboflavin supplementation
DURAN, M, CLEUTJENS, C. B. J. M, KETTING, D, DORLAND, L, DE KLERK, J. B. C, VAN SPRANG, F. J, BERGER, R
Published in Pediatric research (1992)
Published in Pediatric research (1992)
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Beta-mannosidosis in two brothers with hearing loss
Dorland, L, Duran, M, Hoefnagels, F E, Breg, J N, Fabery de Jonge, H, Cransberg, K, van Sprang, F J, van Diggelen, O P
Published in Journal of inherited metabolic disease (01.06.1988)
Published in Journal of inherited metabolic disease (01.06.1988)
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3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal
Gibson, K M, Nyhan, W L, Sweetman, L, Narisawa, K, Lehnert, W, Divry, P, Robinson, B H, Roth, K S, Beemer, F A, van Sprang, F J
Published in European journal of pediatrics (01.10.1988)
Published in European journal of pediatrics (01.10.1988)
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Rapid diagnosis of 3-hydroxy-3-methylglutaryl—coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method
Wanders, R.J.A., Zoeters, P.H.M., Schutgens, R.B.H., de Klerk, J.B.C., Duran, M., Wadman, S.K., van Sprang, F.J., Hemmes, A.M., Voorbrood, B.S.
Published in Clinica chimica acta (31.08.1990)
Published in Clinica chimica acta (31.08.1990)
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Novel storage products in human beta-mannosidosis
Hokke, C H, Duran, M, Dorland, L, van Pelt, J, van Sprang, F J
Published in Journal of inherited metabolic disease (01.05.1990)
Published in Journal of inherited metabolic disease (01.05.1990)
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The cerebro-costo-mandibular syndrome: third report of familial occurrence
Hennekam, R C, Beemer, F A, Huijbers, W A, Hustinx, P A, van Sprang, F J
Published in Clinical genetics (01.08.1985)
Published in Clinical genetics (01.08.1985)
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Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase
Wanders, R J, Duran, M, Ijlst, L, de Jager, J P, van Gennip, A H, Jakobs, C, Dorland, L, van Sprang, F J
Published in The Lancet (British edition) (01.07.1989)
Published in The Lancet (British edition) (01.07.1989)
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A patient with sarcosinaemia
van Sprang, F J, Duran, M, Scholten, H G, Wadman, S K
Published in Journal of inherited metabolic disease (01.12.1986)
Published in Journal of inherited metabolic disease (01.12.1986)
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New defects of pyrimidine metabolism
Wadman, S K, Beemer, F A, de Bree, P K, Duran, M, van Gennip, A H, Ketting, D, van Sprang, F J
Published in Advances in experimental medicine and biology (1984)
Published in Advances in experimental medicine and biology (1984)
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Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine
Wadman, S.K., Duran, M., Ketting, D., Bruinvis, L., van Sprang, F.J., Berger, R., Smit, G.P.A., Steinmann, B., Leonard, J.V., Divry, P., Farriaux, J.P., Cartigny, B.
Published in Clinica chimica acta (30.05.1983)
Published in Clinica chimica acta (30.05.1983)
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Nϵ-(carboxymethyd)lysine, a constituent of human urine
Wadman, S.K., De Bree, P.K., Van Sprang, F.J., Kamerling, J.P., Haverkamp, J., Vliegenthart, J.F.G.
Published in Clinica chimica acta (24.03.1975)
Published in Clinica chimica acta (24.03.1975)
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Chromatographic determination and mass spectrometric identification of γ-glutamylphenylalanine, a urinary constituent in phenylketonuria
Kamerling, J.P., Aarsen, G.J., Duran, M., de Bree, P.K., Van Sprang, F.J., Wadman, S.K.
Published in Clinica chimica acta (28.03.1980)
Published in Clinica chimica acta (28.03.1980)
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A case of formiminoglutamic aciduria. Clinical and biochemical studies
Duran, M, Ketting, D, de Bree, P K, van Sprang, F J, Wadman, S K, Penders, T J, Wilms, R H
Published in European journal of pediatrics (01.07.1981)
Published in European journal of pediatrics (01.07.1981)
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Tyrosinemia and tyrosyluria in healthy prematures: Time courses not vitamin C-dependent
Bakker, H.D., Wadman, S.K., Van Sprang, F.J., Van der Heiden, C., Ketting, D., De Bree, P.K.
Published in Clinica chimica acta (15.05.1975)
Published in Clinica chimica acta (15.05.1975)
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