Branched short-chain dicarboxylic acids in human urine.
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Acidosis↗
Biomedical subjects
O Stokke
Publications and source records attributed to O Stokke.
Application of gas chromatography, mass spectrometry, and computer methods in clinical biochemistry.
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Animals↗
Pyroglutamic aciduria: studies on the enzymic block and on the metabolic origin of pyroglutamic acid.
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Adult↗
Combined use of gas chromatography, mass spectrometry, and computer in diagnosis and studies of metabolic disorders.
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Adult↗
Esophageal hiatus hernia and mental retardation: life-threatening postoperative metabolic acidosis and potassium deficiency linked with a new inborn error of nitrogen metabolism.
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Acidosis↗
Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation.
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Amino Acid Metabolism, Inborn Errors↗
Fatal congenital lactic acidosis in two siblings. II. Biochemical studies in vivo and in vitro.
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Acidosis↗
Screening for metabolic disorders using gas-liquid chromatography, mass spectrometry, and computer technique.
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Acidosis↗
A simple method for preparation of methyl-labelled (-) carnitine.
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Acyltransferases↗
Beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria: a new inborn error of metabolism.
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Butyrates↗
[Metabolism of methylmalonic acid illustrated by a recently discovered inherited disease].
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Diet Therapy↗
Heredopathia atactica polyneuritiformis--an inborn error of lipid metabolism involving the nervous system.
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Fatty Acids↗
Abnormal patterns of urine and serum amino acids in methylmalonic acidemia.
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Age Factors↗
Pyroglutamic aciduria--a new inborn error of metabolism.
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Acidosis↗
Evidence against a CO2-fixation mechanism in the degradation of a beta-methyl-substituted fatty acid in mammals.
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Acetates↗
The degradation of a branched chain fatty acid by alternations between alpha- and beta-oxidations.
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Animals↗
Methylmalonic-acidaemia-hyperglycinaemia.
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Amino Acid Metabolism, Inborn Errors↗
Alpha-oxidation of a beta-methyl-substituted fatty acid in guinea-pig liver mitochondria.
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Animals↗