Exertion of delta-aminolevulinic acid in hereditary tyrosinemia.
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Abdomen↗
Biomedical subjects
S Lindstedt
Publications and source records attributed to S Lindstedt.
Hereditary tyrosinemia. 3. On the differential diagnosis and the lack of effect of early dietary treatment.
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Amino Acid Metabolism, Inborn Errors↗
Enzymatic studies in a case of hereditary tyrosinemia with hepatoma.
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Acyltransferases↗
Studies on the distribution and elimination of [3H8] pyridoxine in mice.
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Animals↗
The origin of inorganic pyrophosphate in urine.
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Animals↗
Studies on the metabolism of the phenolic acids in hereditary tyrosinemia by a gas-liquid chromatographic method.
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Acids↗
Alpha-ketoglutarate and hydroxylation of gamma-butyrobetaine.
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Betaine↗
alpha-Ketoglutarate in biological hydroxylations.
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Journal Article↗
Metabolism of [3H8] pyridoxine in mice.
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Aldehydes↗
The Stockholm prospective study. 1. The initial values for plasma lipids.
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Adolescent↗
Dietary treatment in tyrosinemia (tyrosinosis). With a note on the possible recognition of the carrier state.
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Amino Acid Metabolism, Inborn Errors↗
Studies on the metabolism of lysine and 5-hydroxylysine.
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Alcaligenes↗
Metabolism of 2-amino-5-hydroxyadipic acid in the rat.
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Adipates↗
Studies on the formation of cholic acid in subjects given standardized diet with butter or corn oil as dietary fat.
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Bile Acids and Salts↗
Studies on the metabolism of labeled pyridoxine in man.
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Adult↗
Metabolism of labeled pyridoxine in the rat.
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Animals↗
Determination of lactic dehydrogenase in the urine as an aid to the diagnosis of cancer of the kidney.
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Humans↗
The effect of dietary fat on the turnover of cholic acid and on the composition of the biliary bile acids in man.
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Adult↗