Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome von Wanders, R.J.A., Kos, M., Roest, B., Meijer, A.J., Schrakamp, G., Heymans, H.S.A., Tegelaers, W.H.H., van den Bosch, H., Schutgens, R.B.H., Tager, J.M.

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Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors von Schrakamp, G, Schalkwijk, C G, Schutgens, R B, Wanders, R J, Tager, J M, van den Bosch, H

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Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome von Schutgens, R.B.H., Romeyn, G.J., Wanders, R.J.A., van den Bosch, H., Schrakamp, G., Heymans, H.S.A.

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Ether lipid synthesis and its deficiency in peroxisomal disorders von van den Bosch, H., Schrakamp, G., Hardeman, D., Zomer, A.W.M., Wanders, R.J.A., Schutgens, R.B.H.

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Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome von Schrakamp, G, Roosenboom, C F, Schutgens, R B, Wanders, R J, Heymans, H S, Tager, J M, van den Bosch, H

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Prenatal and perinatal diagnosis of peroxisomal disorders von Schutgens, R. B. H., Schrakamp, G., Wanders, R. J. A., Heymans, H. S. A., Tager, J. M., Bosch, H.

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Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunction von Poll‐The, B. T., Saudubray, J. M., Ogier, H., Schutgens, R. B. H., Wanders, R. J. A., Schrakamp, G., Bosch, H., Trijbels, J. M. F., Poulos, A., Moser, H. W., Eldere, J., Eyssen, H. J.

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Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal β-oxidation enzyme proteins von WANDERS, R. J. A, SCHUTGENS, R. B. H, SCHRAKAMP, G, VAN DEN BOSCH, H, TAGER, J. M, SCHRAM, A. W, HASHIMOTO, T, POLL-THE, B. T, SAUDUBRAU, J. M

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A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells von WANDERS, R. J. A, SCHRAKAMP, G, VAN DEN BOSCH, H, TAGER, J. M, SCHUTGENS, R. B. H

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Neonatal adrenoleukodystrophy: Impaired plasmalogen biosynthesis and peroxisomal β-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fib... von Wanders, R.J.A., Schutgens, R.B.H., Schrakamp, G., Tager, J.M., Van den Bosch, H., Moser, A.B., Moser, H.W.

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Peroxisomal functions in classical Refsum's disease: Comparison with the infantile form of Refsum's disease von Wanders, R.J.A., Heymans, H.S.A., Schutgens, R.B.H., Poll-Thé, B.T., Saudubray, J.M., Tager, J.M., Schrakamp, G., van den Bosch, H.

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Zellweger syndrome: Biochemical procedures in diagnosis, prevention and treatment von Schutgens, R. B. H., Wanders, R. J. A., Heymans, H. S. A., Schram, A. W., Tager, J. M., Schrakamp, G., Bosch, H.

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The cerebro-hepato-renal (Zellweger) syndrome: Prenatal detection based on impaired biosynthesis of plasmalogens von Schutgens, R. B. H., Schrakamp, G., Wanders, R. J. A., Heymans, H. S. A., Moser, H. W., Moser, A. E., Tagers, J. M., Bosch, H. V. D., Aubourm, P.

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Impaired plasmalogen metabolism in infantile Refsum's disease von Poll-Thé, B T, Ogier, H, Saudubray, J M, Schutgens, R B, Wanders, R J, van den Bosch, H, Schrakamp, G

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Prenatal diagnosis of the cerebro‐hepato‐renal (Zellweger) syndrome by detection of an impaired plasmalogen biosynthesis von Schutgens, R. B. H., Heymans, H. S. A., Wanders, R. J. A., Bosch, H., Schrakamp, G.

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Deficiency of dihydroxyacetonephosphate acyltransferase and catalase‐containing particles in patients with infantile refsum's disease von Wanders, R. J. A., Schutgens, R. B. H., Schrakamp, G., Bosch, H., Tager, J. M., Poll‐Thé, B. T., Saudubray, J. M.

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Peroxisomal β-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome von Wanders, Ronald J.A., van Roermund, Carlo W.T., de Vries, Conny T., van den Bosch, Henk, Schrakamp, Gemke, Tager, Joseph M., Schram, AndréW., Schutgens, Ruud B.H.

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Neonatal adrenoleukodystrophy von Wanders, R.J.A., Schutgens, R.B.H., Schrakamp, G., Tager, J.M., Van den Bosch, H., Moser, A.B., Moser, H.W.

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Prenatal detection of Zellweger syndrome von Schutgens, R B, Heymans, H S, Wanders, R J, vd Bosch, H, Schrakamp, G

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PRENATAL DETECTION OF ZELLWEGER SYNDROME von Schutgens, R.B.H., Heymans, H.S.A., Wanders, R.J.A., Bosch, H.V.D., Schrakamp, G.

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