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scurvy/tyrosine

Veza se sprema u međuspremnik
ČlanciKlinička ispitivanjaPatenti
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Tyrosine metabolism in infantile scurvy.

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Tyrosine metabolism in human scurvy.

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Metabolism of tyrosine in experimental megaloblastic anemia and in scurvy in the monkey.

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[Studies on phenylalanine & tyrosine metabolism in scurvy in children].

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Effect of citrovorum factor upon tyrosine metabolism in clinical scurvy.

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Some investigations on the metabolism of phenylalanine and tyrosine in children with vitamin C deficiency.

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THE METABOLISM OF l-TYROSINE IN INFANTILE SCURVY.

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Role of ascorbic acid on tyrosine hydroxylase activity in the adrenal gland of guinea pig.

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The decrease of tyrosine hydroxylase activity in adrenal homogenate in scurvy was recovered after the administration of ascorbic acid. The causes of the increase in the enzyme activity after the administration of ascorbic acid have been studied. 1. No significant elevation in the enzyme activity was

Tyrosinosis: a new variant.

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ABNORMALITIES OF TYROSINE METABOLISM ARE DISCUSSED UNDER FOUR HEADINGS: (1) accumulation of tyrosine and its metabolites secondary to severe liver damage, vitamin C deficiency, etc.; (2) transient neonatal tyrosinemia; (3) hereditary tyrosinosis with hepatorenal dysfunction where elevation of

Neonatal hypertyrosinemia and evidence for deficiency of ascorbic acid in Arctic and subarctic peoples.

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Hypertyrosinemia tyrosine concentration in whole blood greater than 0.42 mmol/l or 7.5 mg/dl is prevalent among lnuit newborn of the Canadian Eastern Arctic. The rate was 14.8 per 100 newborn between January 1970 and December 1972 (first survey period) and 6.2/100 between January 1973 and September
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