SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE von Wanders, R.J.A., Duran, M., Ijlst, L., De Jager, J.P., Van Gennip, A.H., Jakobs, C., Dorland, L., Van Sprang, F.J.

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Head circumference of children with phenylketonuria during dietary treatment von Sprang, F.J. van

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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 von 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.

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HEAD CIRCUMFERENCE OF CHILDREN WITH PHENYLKETONURIA DURING DIETARY TREATMENT von Van Sprang, F.J

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Identification of genotypes of carrier variants with diminished activity of galactose-1-phosphate uridyltransferase von Van Der Heiden, C., Desplanque, J., Beemer, F.A., De Klerk, J.B.C., Van Sprang, F.J.

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Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine von 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.

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LOW SERUM-TYROSINE IN PATIENTS WITH PHENYLKETONURIA ON DIETARY TREATMENT von Brouwer, M., De Bree, P.K., Van Sprang, F.J., Wadman, S.K.

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Abnormal tyrosine and phenylalanine metabolism in patients with tyrosyluria and phenylketonuria; gas-liquid chromatographic analysis of urinary metabolites von Wadman, S.K., Van Der Heiden, C., Ketting, D., Van Sprang, F.J.

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Tyrosinemia and tyrosyluria in healthy prematures: Time courses not vitamin C-dependent von Bakker, H.D, Wadman, S.K, Sprang, F.J. van, Heiden, C. van der, Ketting, D, Bree, P.K. de

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Fructose-1,6-diphosphatase deficiency: Another enzyme defect which can present itself with the clinical features of “tyrosinosis” von Bakker, H.D, Bree, P.K. de, Ketting, D, Sprang, F.J. van, Wadman, S.K

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Nϵ-(carboxymethyd)lysine, a constituent of human urine von Wadman, S.K., De Bree, P.K., Van Sprang, F.J., Kamerling, J.P., Haverkamp, J., Vliegenthart, J.F.G.

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Chromatographic determination and mass spectrometric identification of γ-glutamylphenylalanine, a urinary constituent in phenylketonuria von Kamerling, J.P., Aarsen, G.J., Duran, M., de Bree, P.K., Van Sprang, F.J., Wadman, S.K.

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Tyrosinemia and tyrosyluria in healthy prematures: Time courses not vitamin C-dependent von Bakker, H.D., Wadman, S.K., Van Sprang, F.J., Van der Heiden, C., Ketting, D., De Bree, P.K.

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Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normals von Wadman, S.K., de Bree, P.K., van Der Heiden, C., van Sprang, F.J.

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Fructose-1,6-diphosphatase deficiency: Another enzyme defect which can present itself with the clinical features of “tyrosinosis” von Bakker, H.D., De Bree, P.K., Ketting, D., Van Sprang, F.J., Wadman, S.K.

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Dietary correction of histidinemia in older children possible von Wadman, S.K., De Bree, P.K., Van Biervliet, J.P.G.M., Van Sprang, F.J.

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Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria von Donker, D.N.J, Reits, D, Sprang, F.J. van, Storm van Leeuwen, W, Wadman, S.K

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Chromatographic determination and mass spectrometric identification of γ-glutamylphenylalanine, a urinary constituent in phenylketonuria von Kamerling, J.P, Aarsen, G.J, Duran, M, Bree, P.K. de, Sprang, F.J. van, Wadman, S.K

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Abnormal tyrosine and phenylalanine metabolism in patients with tyrosyluria and phenylketonuria; gas-liquid chromatographic analysis of urinary metabolites von Wadman, S.K, Heiden, C. van der, Ketting, D, Sprang, F.J. van

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Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria von Donker, D.N.J., Reits, D., Van Sprang, F.J., Van Leeuwen, W.Storm, Wadman, S.K.

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