P. K. de Bree

发表

2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate--a pitfall in the diagnosis of sulfite oxidase deficiency.

M. Durán, S. K. Wadman, R. Fokkens, 1981, Clinica chimica acta; international journal of clinical chemistry.

D-Glyceric acidemia in a patient with chronic metabolic acidosis.

M. Durán, H. Bremer, D. Ketting, 1976, Clinica chimica acta; international journal of clinical chemistry.

Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis".

S. K. Wadman, H. Bakker, P. K. de Bree, 1974, Clinica chimica acta; international journal of clinical chemistry.

Purine nucleoside phosphorylase deficiency associated with selective cellular immunodeficiency.

S. K. Wadman, J. W. Stoop, B. Zegers, 1977, The New England journal of medicine.

A patient with purine nucleoside phosphorylase deficiency: enzymological and metabolic aspects.

S. K. Wadman, J. Akkerman, J. W. Stoop, 1977, Clinica chimica acta; international journal of clinical chemistry.

Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism.

M. Durán, S. K. Wadman, F. Beemer, 1984, Clinica chimica acta; international journal of clinical chemistry.

New defects of pyrimidine metabolism.

M. Durán, D. Ketting, S. K. Wadman, 1984, Advances in Experimental Medicine and Biology.

Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependent.

D. Ketting, S. K. Wadman, C. van der Heiden, 1975, Clinica chimica acta; international journal of clinical chemistry.

Detection of inherited adenylosuccinase deficiency by two dimensional thin layer chromatography of urinary imidazoles.

M. Durán, S. K. Wadman, P. K. de Bree, 1986, Advances in experimental medicine and biology.

Azetidine-2-carboxylic acid contaminated dietary proline as a cause of urinary excretion of 4-amino-2-(S-cysteinyl)butyric acid in patients on oral treatment with a synthetic diet.

M. Durán, H. Bremer, S. K. Wadman, 1983, Journal of chromatography.

Urinary and faecal excretion of metabolites of tyrosine and phenylalanine in a patient with cystic fibrosis and severely impaired amino acid absorption.

D. Ketting, S. K. Wadman, C. van der Heiden, 1971, Clinica chimica acta; international journal of clinical chemistry.

Gas chromatographic analysis of urinary volatile phenols in patients with gastro-intestinal disorders and normals.

M. Durán, D. Ketting, S. K. Wadman, 1973, Clinica chimica acta; international journal of clinical chemistry.

Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles.

D. Ketting, S. K. Wadman, L. Monnens, 1977, Pediatric research.

Urinary excretion of 3 -methylxanthine and related compounds in children.

S. K. Wadman, J. Vliegenthart, C. van der Heiden, 1973, Clinica chimica acta; international journal of clinical chemistry.

Urinary excretion of orotic acid, orotidine and other pyrimidines in a patient with purine nucleoside phosphorylase deficiency.

S. K. Wadman, J. W. Stoop, B. Zegers, 1979, Clinica chimica acta; international journal of clinical chemistry.

Prenatal diagnosis of purine nucleoside phosphorylase deficiency in the first and second trimesters of pregnancy

M. Durán, W. Kleijer, F. Los, 1989, Prenatal diagnosis.

Urinary purines in a patient with a severely defective T cell immunity and a purine nucleoside phosphorylase deficiency.

S. K. Wadman, J. W. Stoop, B. Zegers, 1977, Advances in experimental medicine and biology.

Increased urinary imidazolepropionic acid, N-acetylhistamine and other imidazole compounds in patients with intestinal disorders.

S. K. Wadman, C. van der Heiden, P. K. de Bree, 1972, Clinica chimica acta; international journal of clinical chemistry.

Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normals.

S. K. Wadman, C. van der Heiden, P. K. de Bree, 1971, Clinica chimica acta; international journal of clinical chemistry.

Rapid, high-resolution, two-dimensional amino acid chromatography on micro scale chromatograms.

S. K. Wadman, P. K. de Bree, H. D. de Jonge, 1969, Clinica chimica acta; international journal of clinical chemistry.

Lanthionine detected in human urine.

S. K. Wadman, J. Kamerling, P. K. de Bree, 1978, Clinica chimica acta; international journal of clinical chemistry.

Three new cases of Histidinemia. Clinical and biochemical data.

S. K. Wadman, G. V. van Stekelenburg, P. K. de Bree, 1966, Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete.

Dietary correction of histidinemia in older children possible.

S. K. Wadman, J. Van Biervliet, P. K. de Bree, 1973, Clinica chimica acta; international journal of clinical chemistry.

Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental development.

D. Ketting, S. K. Wadman, C. van der Heiden, 1975, Clinica chimica acta; international journal of clinical chemistry.

Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purines.

M. Durán, S. K. Wadman, P. K. de Bree, 1986, Clinica chimica acta; international journal of clinical chemistry.

Two-dimensional thin-layer chromatography for the screening of disorders of purine and pyrimidine metabolism.

S. K. Wadman, A. V. van Gennip, P. K. de Bree, 1978, Clinica chimica acta; international journal of clinical chemistry.

A sensitive automatic determination of protein in urine serum and cerebrospinal fluid.

S. K. Wadman, P. K. de Bree, J. A. Klosse, 1971, Clinica chimica acta; international journal of clinical chemistry.

O-phosphohydroxylysinuria: a new inborn error of metabolism?

M. Durán, L. Dorland, P. K. de Bree, 1990, Clinica chimica acta; international journal of clinical chemistry.