The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern
- 23 April 1982
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 120 (3) , 341-353
- https://doi.org/10.1016/0009-8981(82)90375-8
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- The early recognition of the 21-hydroxylase deficiency variety of congenital adrenal hyperplasiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1980
- Analysis of glucocorticoid metabolites in the neonatal period: Catabolism of cortisone acetate by an infant with 21-hydroxylase deficiencyClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- The identification and quantification of three new 6α-hydroxylated corticosteroids in human neonatal urine.Steroids, 1978
- Polar corticosteroids in human neonatal urine; Synthesis and gas chromatography-mass spectrometry of ring a reduced 6-hydroxylate corticosteroidsSteroids, 1978
- Studies on steroidogenesis and its regulation in human fetal adrenal and testisJournal of Steroid Biochemistry, 1977
- Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of lifeClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- STEROIDS IN NEWBORNS AND INFANTSActa Endocrinologica, 1973
- An all-glass solid sampling device for open tubular columns in gas chromatographyChromatographia, 1972
- Steroids in newborns and infants identification of steroids in urine from newborn infantsSteroids, 1971
- Sterods in Newborns and InfantsEuropean Journal of Biochemistry, 1969