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

Clinica chimica acta, 1991-12, Vol.204 (1), p.79-86

1991

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

Journal of chromatography, 1986-01, Vol.382, p.19-30

1986

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Glutaric aciduria type II: Report on a previously undescribed metabolic disorder

Clinica chimica acta, 1976-01, Vol.66 (2), p.227-239

1976

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Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolism

The Journal of pediatrics, 1982-10, Vol.101 (4), p.551-554

1982

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

Clinica chimica acta, 1978-05, Vol.86 (1), p.7-20

1978

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

Clinica chimica acta, 1975-01, Vol.58 (3), p.257-269

1975

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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

Journal of chromatography, 1983-01, Vol.277, p.41-51

1983

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

Clinica chimica acta, 1994-10, Vol.230 (1), p.91-99

1994

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

Journal of chromatography. Biomedical applications, 1981-02, Vol.222 (2), p.276-283

1981

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

Clinica chimica acta, 1984-08, Vol.141 (2), p.227-234

1984

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

Clinica chimica acta, 1986-05, Vol.156 (3), p.279-287

1986

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

Journal of chromatography, 1986-09, Vol.381 (2), p.401-405

1986

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

Clinica chimica acta, 1985-11, Vol.152 (3), p.253-260

1985

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

Clinica chimica acta, 1987-06, Vol.165 (2), p.197-204

1987

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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

Clinica chimica acta, 1990-08, Vol.189 (3), p.327-334

1990

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O-Phosphohydroxylysinuria: a new inborn error of metabolism?

Clinica chimica acta, 1990-05, Vol.188 (3), p.221-226

1990

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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

Clinica chimica acta, 1988-01, Vol.171 (1), p.49-61

1988

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Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia

Clinica chimica acta, 1981-07, Vol.114 (1), p.37-44

1981

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

Clinica chimica acta, 1986-08, Vol.159 (1), p.11-16

1986

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

Clinica chimica acta, 1983-10, Vol.134 (1), p.77-83

1983

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

Clinica chimica acta, 1985-02, Vol.146 (1), p.29-35

1985

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

Clinica chimica acta, 1983-04, Vol.129 (3), p.303-309

1983

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

Clinica chimica acta, 1978-12, Vol.90 (2), p.195-200

1978

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The variability of metabolite excretion in propionicacidaemia

Clinica chimica acta, 1978-01, Vol.82 (1), p.93-99

1978

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Gas chromatography of urinary N-phenylacetylglutamine

Journal of chromatography, 1979-10, Vol.164 (2), p.217-221

1979

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

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

Glutaric aciduria type II: Report on a previously undescribed metabolic disorder

Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolism

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

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

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

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

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

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

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

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

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

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

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

O-Phosphohydroxylysinuria: a new inborn error of metabolism?

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

Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia

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

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

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

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

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

The variability of metabolite excretion in propionicacidaemia

Gas chromatography of urinary N-phenylacetylglutamine

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