Defect in synthesis of epinephrine in premature infants with tyrosinemia
- 1 March 1971
- journal article
- Published by Elsevier in Metabolism
- Vol. 20 (3) , 247-254
- https://doi.org/10.1016/0026-0495(71)90107-7
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Dietary Treatment in Tyrosinemia (Tyrosinosis)American Journal of Diseases of Children, 1967
- Aminoacidemia of PrematurityAmerican Journal of Diseases of Children, 1966
- Tyrosinemia: An inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal tubular defects (de Toni-Debré-Fanconi syndrome)The Journal of Pediatrics, 1965
- The Plasma Tyrosine Levels of Premature BabiesArchives of Disease in Childhood, 1964
- Serotonin Deficiency in Infancy as One Cause of a Mental Defect in PhenylketonuriaScience, 1964
- Determination of 3-methoxy-4-hydroxymandelic acid in urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1962
- Developmental changes of p-hydroxyphenylpyruvate-oxidase activity in mammalian liverBiochimica et Biophysica Acta, 1961
- A simple analysis for normetanephrine and metanephrine in urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1960
- A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. II. SPONTANEOUS OCCURRENCE AND ERADICATION BY VITAMIN C 12Journal of Clinical Investigation, 1941
- A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. I. IDENTIFICATION AND ASSAY OF INTERMEDIARY PRODUCTS 12Journal of Clinical Investigation, 1941