S. K. Wadman

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Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase.

M. Durán, R. Schutgens, H. Heymans, 1979, The Journal of pediatrics.

Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolism.

M. Durán, D. Ketting, S. K. Wadman, 1987, Clinica chimica acta; international journal of clinical chemistry.

A VARIANT FORM OF BRANCHED‐CHAIN KETO ACIDURIA

S. K. Wadman, J. Horst, 1971, Acta paediatrica Scandinavica.

Human molybdenum cofactor deficiency.

S. K. Wadman, K. Rajagopalan, J. Johnson, 1993, Advances in experimental medicine and biology.

Report of a Patient with Severe, Chronic Lactic Acidaemia and Pyruvate Carboxylase Deficiency

D. Ketting, S. K. Wadman, J. Willemse, 1977, Developmental medicine and child neurology.

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.

Stable isotope dilution analysis of succinylacetone using electron capture negative ion mass fragmentography: an accurate approach to the pre- and neonatal diagnosis of hereditary tyrosinemia type I.

S. K. Wadman, L. Dorland, C. Jakobs, 1988, 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.

An exceptional case of tyrosinosis.

D. Ketting, S. K. Wadman, J. Maas, 2008, Journal of mental deficiency research.

Urinary excretion of methylated purines in man and in the rat after the administration of theophylline.

D. Ketting, S. K. Wadman, J. Grift, 1979, Journal of chromatography.

Two sistes with isovaleric acidaemia, multiple attacks of ketoacidosis and normal development

M. Durán, D. Ketting, S. K. Wadman, 1979, European Journal of Pediatrics.

Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid

M. Durán, S. K. Wadman, W. Nyhan, 2004, European Journal of Pediatrics.

Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids.

M. Durán, D. Ketting, S. K. Wadman, 1985, The Journal of pediatrics.

A new method for the determination of L-dopa and 3-O-methyldopa in plasma and cerebrospinal fluid using gas chromatography and electron capture negative ion mass spectrometry.

S. K. Wadman, C. Cramers, A. D. de Jong, 1988, 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.

Purine nucleoside phosphorylase deficiency associated with cellular immunodeficiency: immunological studies during treatment

S. K. Wadman, J. W. Stoop, B. Zegers, 1979 .

Group tests for selective screening of inborn errors of metabolism

M. Durán, S. K. Wadman, L. Dorland, 2005, European Journal of Pediatrics.

Gas chromatographic analysis of urinary tyrosine and phenylalanine metabolites in patients with gastrointestinal disorders.

M. Durán, D. Ketting, S. K. Wadman, 1971, Clinica chimica acta; international journal of clinical chemistry.

Systemic carnitine deficiency: Benefit of oral carnitine supplements vs. persisting biochemical abnormalities

M. Durán, S. K. Wadman, Mar Durán, 1984, European Journal of Pediatrics.

Nϵ-(carboxymethyd)lysine, a constituent of human urine

S. K. Wadman, J. Vliegenthart, J. Kamerling, 1975 .

Erythrocyte metabolism in purine nucleoside phosphorylase deficiency after enzyme replacement therapy by infusion of erythrocytes.

D. Martin, S. K. Wadman, J. W. Stoop, 1980, The Journal of clinical investigation.

The occurrence of lactyl lactate and succinyl lactate in the urine of patients screened for inherited metabolic disease.

D. Ketting, S. K. Wadman, L. Sweetman, 1985, Clinica chimica acta; international journal of clinical chemistry.

Three New Cases of Histidinemia

S. K. Wadman, G. J. Stekelenburg, F. J. Sprang, 1967 .

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.

Abnormal tyrosine and phenylalanine metabolism in patients with tyrosyluria and phenylketonuria; gas-liquid chromatographic analysis of urinary metabolites.

D. Ketting, S. K. Wadman, C. Heiden, 1971 .

The estimation of phenylalanine in serum by paper chromatography at elevated temperatures.

S. K. Wadman, J. M. va de HEUVEL, 1960, 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.

Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia.

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

Abnormally Low α2- and β-Globulin Levels in Serious Hepatic Insufficiency

S. K. Wadman, L. Leeuwen, K. Brandt, 2009 .

Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis

M. Durán, S. K. Wadman, P. Cock, 1988, European Journal of Pediatrics.

Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome.

S. K. Wadman, S. Kolvraa, N. Gregersen, 1985, The Journal of pediatrics.

A New Case of Purine Nucleoside Phosphorylase Deficiency: Enzymologic, Clinical, and Immunologic Characteristics

W. Kuis, M. Durán, S. K. Wadman, 1987, Pediatric Research.

D-Glyceric Acidemia: An Inborn Error Associated with Fructose Metabolism

M. Durán, D. Ketting, S. K. Wadman, 1987, Pediatric Research.

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.

Nϵ(β-aspartyl)lysinuria in children with various pathological conditions

M. Durán, S. K. Wadman, J. Kamerling, 1978 .

The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.

M. Durán, R. Schutgens, D. Ketting, 1982, Biomedical mass spectrometry.

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.

Gas chromatography method for the separation of amino acids enantiomers in plasma and urine. Application in a case of short bowel syndrome.

M. Durán, D. Ketting, S. K. Wadman, 1991, Clinica chimica acta; international journal of clinical chemistry.

Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.

M. Durán, S. K. Wadman, F. Beemer, 1980, Proceedings of the National Academy of Sciences of the United States of America.

5‐OXOPROLINURIA DUE TO HEREDITARY 5‐OXOPROLINASE DEFICIENCY IN TWO BROTHERS–A NEW INBORN ERROR OF THE γ‐GLUTAMYL CYCLE

M. Durán, S. K. Wadman, J. V. Gool, 1981, Acta paediatrica Scandinavica.

Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?

M. Durán, S. K. Wadman, F. Beemer, 1978, Journal of Inherited Metabolic Disease.

Densitometric determination of catecholamine metabolites and 5-hydroxy-indoleacetic acid after two-dimensional thin-layer chromatography on cellulose.

S. K. Wadman, K. Breebaart, A. M. Haan, 1972, Clinica chimica acta; international journal of clinical chemistry.

Gas chromatographic determination of urinary vanilglycolic acid, vanilglycol, vanilacetic acid and vanillactic acid-chemical parameters for the diagnosis of neurogenic tumours and the evaluation of their treatment.

P. Voûte, D. Ketting, S. K. Wadman, 1976, Clinica chimica acta; international journal of clinical chemistry.

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.

Intracellular purine and pyrimidine nucleotide pools of human T and B lymphocytes.

M. Durán, S. K. Wadman, G. Rijkers, 1986 .

Mechanisms of deoxyguanosine toxicity for human T and B lymphocytes.

S. K. Wadman, B. Zegers, G. Staal, 1986, Advances in experimental medicine and biology.

The effect of deoxyguanosine on human lymphocyte function. I. Analysis of the interference with lymphocyte proliferation in vitro.

S. K. Wadman, J. W. Stoop, B. Zegers, 1984, Journal of immunology.

Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency.

M. Durán, D. Ketting, S. K. Wadman, 1988, Clinical chemistry.

Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs

M. Durán, D. Ketting, S. K. Wadman, 1982, European Journal of Pediatrics.

Urinary D-4-hydroxyphenyllactate, D-phenyllactate and D-2-hydroxyisocaproate, abnormalities of bacterial origin

M. Durán, D. Ketting, S. K. Wadman, 1987, Journal of Inherited Metabolic Disease.

Glutaric aciduria type II: report on a previously undescribed metabolic disorder.

H. Bremer, D. Ketting, S. K. Wadman, 1976, Clinica chimica acta; international journal of clinical chemistry.

Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts.

M. Durán, R. Schutgens, H. A. Veder, 1978, Clinica chimica acta; international journal of clinical chemistry.

Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia

M. Durán, D. Ketting, S. K. Wadman, 1978, Journal of Inherited Metabolic Disease.

Organic aciduria in late-onset biotin-responsive multiple carboxylase deficiency

S. K. Wadman, L. Mienie, C. J. Reinecke, 1985, Journal of Inherited Metabolic Disease.

The variability of metabolite excretion in propionicacidaemia.

M. Durán, D. Ketting, S. K. Wadman, 1978, Clinica chimica acta; international journal of clinical chemistry.

Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method.

R. Wanders, M. Durán, R. Schutgens, 1990, Clinica chimica acta; international journal of clinical chemistry.

Organic acidurias: approach, results and clinical relevance.

M. Durán, S. K. Wadman, J. Kamerling, 1982, Ciba Foundation symposium.

A new patient with dicarboxylic aciduria suggestive of medium-chain acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome

M. Durán, C. Pérez-Cerdá, S. K. Wadman, 1984, Journal of Inherited Metabolic Disease.

Gas chromatography of urinary N-phenylacetylglutamine.

D. Ketting, S. K. Wadman, J. Kamerling, 1979, Journal of chromatography.

3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine.

M. Durán, R. Schutgens, H. Heymans, 1979, The Journal of pediatrics.

GLUTARIC ACIDURIA ‘TYPE II’

H. Bremer, S. K. Wadman, H. Przyrembel, 1975, Pediatric Research.

The urinary excretion of ethylmalonic acid: what level requires further attention?

M. Durán, F. Walther, S. K. Wadman, 1983, Biochemical medicine.

A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolism.

M. Durán, S. K. Wadman, M. Rolland, 1983, Clinica chimica acta; international journal of clinical chemistry.

Methylmalonate excretion in a pregnancy at risk for methylmalonic acidaemia.

M. Durán, S. K. Wadman, H. Bakker, 1978, Clinica chimica acta; international journal of clinical chemistry.

Urinary purines and pyrimidines in patients with hyperammonemia of various origins.

S. K. Wadman, J. Grift, A. V. van Gennip, 1980, Clinica chimica acta; international journal of clinical chemistry.

REVERSIBLE HYPOGAMMAGLOBULINAEMIA IN CYANOCOBALAMIN (B12) DEFICIENCY.

S. K. Wadman, G. Meester, G. Slagboom, 2009, Acta medica Scandinavica.

Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)

H. Bremer, S. K. Wadman, J. Versieck, 1986, European Journal of Pediatrics.

Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels

M. Durán, H. Bremer, D. Ketting, 1979, European Journal of Pediatrics.

D-lactic aciduria, an inborn error of metabolism?

M. Durán, S. K. Wadman, J. Kamerling, 1977, Clinica chimica acta; international journal of clinical chemistry.

L-2-Hydroxyglutaric aciduria: an inborn error of metabolism?

M. Durán, S. K. Wadman, J. Kamerling, 1980, Journal of Inherited Metabolic Disease.

Determination of the absolute configuration of some biologically important urinary 2-hydroxydicarboxylic acids by capillary gas--liquid chromatography.

M. Durán, D. Ketting, S. K. Wadman, 1981, Journal of chromatography.

Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies.

H. Bremer, S. K. Wadman, H. Przyrembel, 1975, 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.

A retrospective study of a patient with homozygous form of acute intermittent porphyria

J. Deybach, S. K. Wadman, B. Grandchamp, 1990, Journal of Inherited Metabolic Disease.

Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency

S. K. Wadman, H. Bakker, C. Heiden, 1978, European Journal of Pediatrics.

Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria

S. K. Wadman, B. Grandchamp, Y. Nordmann, 1990, Journal of Inherited Metabolic Disease.

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.

Clinical and biochemical studies of high-dose thymidine treatment in patients with solid tumors

J. Schornagel, S. K. Wadman, H. Pinedo, 2005, Journal of Cancer Research and Clinical Oncology.

α-Ketoadipic aciduria — a new inborn defect of lysine degradation

H. Bremer, S. K. Wadman, H. Przyrembel, 1976 .

3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal

M. Durán, S. K. Wadman, K. Gibson, 1988, European Journal of Pediatrics.

Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria.

M. Durán, S. K. Wadman, K. Gibson, 1986, The Journal of clinical investigation.

Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism.

M. Durán, D. Ketting, S. K. Wadman, 1982, The Journal of pediatrics.

Familial hyperlysinaemia due to L-lysineα-ketoglutarate reductase deficiency: Results of attempted treatment

S. K. Wadman, J. P. Biervliet, C. Heiden, 1978, Journal of Inherited Metabolic Disease.

The effect of deoxycytidine and tetrahydrouridine in purine nucleoside phosphorylase deficiency.

W. Kuis, M. Durán, S. K. Wadman, 1984, Advances in experimental medicine and biology.

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.

The absolute configuration of urinary 2-hydroxybutyric acid in patients with ketosis and lactic acidosis.

M. Durán, D. Ketting, S. K. Wadman, 1978, Clinica chimica acta; international journal of clinical chemistry.

Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylase

M. Durán, S. K. Wadman, J. Koster, 1979, Journal of Inherited Metabolic Disease.

Treatment of a Patient with Histidinemia

S. K. Wadman, F. J. Sprang, 1967, Acta paediatrica Scandinavica.

Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency

M. Durán, S. K. Wadman, W. Endres, 1988, European Journal of Pediatrics.

An approach to the restoration of T cell function in a purine nucleoside phosphorylase deficient patient.

S. K. Wadman, J. W. Stoop, B. Zegers, 1978, Ciba Foundation symposium.

Sulfite oxidase deficiency and the detection of urinary sulfite

S. K. Wadman, B. Cats, P. Bree, 1983, European Journal of Pediatrics.

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.

Purine nucleoside phosphorylase deficiency associated with cellular immunodeficiency: metabolic studies during treatment

S. K. Wadman, J. W. Stoop, B. Zegers, 1979 .

Red cell metabolism in purine nucleoside phosphorylase deficiency after enzyme replacement therapy.

S. K. Wadman, J. W. Stoop, B. Zegers, 1978, Monographs in human genetics.

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.

Congenital Neuroblastoma

P. Voûte, S. K. Wadman, W. V. van Putten, 1970, Clinical pediatrics.

Linear relationship between the R- and S-enantiomers of β-aminoisobutyric acid in human urine

S. K. Wadman, J. Kamerling, P. Bree, 1981 .

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.

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

M. Durán, S. K. Wadman, F. Beemer, 1985, Journal of Inherited Metabolic Disease.

Occurrences of methylmalonic aciduria and Hartnup disorder in the same family

M. Durán, S. K. Wadman, V. Shih, 1984, Clinical genetics.

Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids.

M. Durán, D. Ketting, S. K. Wadman, 1985, Clinica chimica acta; international journal of clinical chemistry.

[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency].

S. K. Wadman, N. Abeling, J. Van Biervliet, 1977, Archives francaises de pediatrie.

Two-dimensional electrophoresis of urinary mucopolysaccharides on cellulose acetate after N-cetylpyridiniumchloride (CPC) precipitation: a method suitable for the routine laboratory.

S. K. Wadman, N. Abeling, A. V. van Gennip, 1974, 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.

ANTENATAL DIAGNOSIS OF COMBINED XANTHINE AND SULPHITE OXIDASE DEFICIENCIES

S. K. Wadman, J. Johnson, J. Saudubray, 1983, The Lancet.

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.

Maternal PKU syndrome in an exceptional family with unexpected PKU

S. K. Wadman, E. Meuleman, J. Klerk, 1987, Journal of Inherited Metabolic Disease.

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.

Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria.

D N Donker, D Reits, F J Van Sprang, 1979, Electroencephalography and clinical neurophysiology.

Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.

M. Durán, S. K. Wadman, J. Saudubray, 1986, Pediatrics.

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.

An automated chromatographic system for the combined analysis of urinary peptides and amino acids

S. K. Wadman, J. Vliegenthart, P. Bree, 1972 .

Metabolic findings in a patient with adenosine deaminase deficiency and severe combined immunodeficiency.

S. K. Wadman, A. Leyva, A. Signoretti, 1984, Advances in Experimental Medicine and Biology.

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.

Urinary excretion of homocitric acid and methylhomocitric acid in propionic acidaemia: minor metabolic products of the citrate synthase aldol condensation reaction.

M. Durán, S. K. Wadman, W. D. De Wet, 1994, Clinica chimica acta; international journal of clinical chemistry.

A patient with alpha-ketoadipic and alpha-aminoadipic aciduria.

M. Durán, S. K. Wadman, F. Beemer, 1984, Journal of inherited metabolic disease.

Stable isotope dilution analysis of orotic acid and uracil in amniotic fluid.

S. K. Wadman, W. Nyhan, C. Jakobs, 1984, Clinica chimica acta; international journal of clinical chemistry.

Kinetic Study of Catecholamine Metabolism in Hereditary Progressive Dystonia

S. K. Wadman, R. Ouvrier, A. D. de Jong, 1989, Neuropediatrics.

Identification of the stereoisomeric configurations of methylcitric acid produced bysi-citrate synthase and methylcitrate synthase using capillary gas chromatography-mass spectrometry

M. Durán, D. Ketting, S. K. Wadman, 1994, Journal of Inherited Metabolic Disease.

A Fœtal Form of Myoglobin

S. K. Wadman, J. Jonxis, 1952, Nature.

Determination of acidic catecholamine metabolites in plasma and cerebrospinal fluid using gas chromatography-negative-ion mass spectrometry.

S. K. Wadman, C. Cramers, A. D. de Jong, 1986, Journal of chromatography.

LOW SERUM-TYROSINE IN PATIENTS WITH PHENYLKETONURIA ON DIETARY TREATMENT

S. K. Wadman, F. J. Sprang, P. Bree, 1977, The Lancet.

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.

Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalities

M. Durán, D. Ketting, S. K. Wadman, 1982, Journal of Inherited Metabolic Disease.

Quantitative gas chromatographic determination of urinary hydantoin-5-propionic acid in patients with disorders of folate/vitamin B12 metabolism.

M. Durán, S. K. Wadman, L. Bruinvis, 1986, Journal of chromatography.

3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

M. Durán, D. Ketting, S. K. Wadman, 1980, Clinica chimica acta; international journal of clinical chemistry.

Glutaric Aciduria Type I I

S. K. Wadman, F. Beemer, U. Wendel, 2012 .

Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenase.

S. K. Wadman, D. Danks, A. Niederwieser, 1978, Clinica chimica acta; international journal of clinical chemistry.

1,6-anhydro-β-d-glucopyranose (β-glucosan), a constituent of human urine

D. Ketting, S. K. Wadman, L. Dorland, 1986 .

Isovalerylglucuronide, a new urinary metabolite in isovaleric acidemia. Identification problems due to rearrangement reactions.

M. Durán, D. Ketting, S. K. Wadman, 1983, Clinica chimica acta; international journal of clinical chemistry.

The differential diagnosis of dicarboxylic aciduria

M. Durán, D. Ketting, S. K. Wadman, 1984, Journal of Inherited Metabolic Disease.

(2-Ethoxyethoxy)acetic acid: an unusual compound found in the gas chromatographic analysis of urinary organic acids.

M. Durán, D. Ketting, S. K. Wadman, 1977, Clinica chimica acta; international journal of clinical chemistry.

A patient with α-ketoadipic and α-aminoadipic aciduria

M. Durán, S. K. Wadman, F. Beemer, 1984, Journal of Inherited Metabolic Disease.

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

M. Durán, D. Ketting, S. K. Wadman, 1983, Clinica chimica acta; international journal of clinical chemistry.

Propionic acid, an artefact which can leave methylmalonic acidemia undiscovered.

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

Beta-p-hydroxyphenylhydracrylic acid as a urinary constituent in a patient with gastrointestinal disease.

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

Direct identification of propionylcarnitine in propionic acidaemia: Biochemical and clinical results of oral carnitine supplementation

M. Durán, D. Ketting, S. K. Wadman, 1986, Journal of Inherited Metabolic Disease.

Trimethylaminuria, diagnosed by gas chromatography with nitrogen detection

M. Durán, S. K. Wadman, L. Dorland, 1987, Journal of Inherited Metabolic Disease.

Letter: Base excess and organic acidaemia.

M. Durán, S. K. Wadman, G. V. van Stekelenburg, 1974, Lancet.