39 research outputs found
Duplication of the CYP21A2 gene complicaties mutations analysis of steroid 21-hydrxylase deficiency: characteristics of three unusual haplotypes
No full textDuplication of the CYP21A2 gene complicaties mutations analysis of steroid 21-hydrxylase deficiency: characteristics of three unusual haplotypes
No full textCYP21 and CYP21P variability in steroid 21-hydroxylase deficiency patients and in the general population in the Netherlands
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Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency
No full textEFFECT OF DEXAMETHASONE ON PROTEIN METABOLISM IN INFANTS WITH BRONCHOPULMONARY DYSPLASIA.
No full textCONVERSION OF OCTANOIC ACID INTO LONG-CHAIN SATURED FATTY ACID IN PREMATURE INFANTS FED A FORMULA CONTAINING MEDIUM-CHAIN TRIGLYCERIDES.
No full textEnergy utilization and growth in breast-fed and formula-fed infants measured prospectively during the first year of life
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