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. 1969 Feb;44(233):138–139.

Salt-losers and Non Salt-losers in Congenital Adrenal Hyperplasia

B T Rudd
PMCID: PMC2020232

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. COPPAGE W. S., Jr, LIDDLE G. W. Metabolic studies with a steroid isolated from the urine of patients with "salt-losing" congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1960 May;20:729–734. doi: 10.1210/jcem-20-5-729. [DOI] [PubMed] [Google Scholar]
  2. DEGENHART H. J., VISSER H. K., WILMINK R., CROUGHS W. ALDOSTERONE- AND CORTISOL SECRETION RATES IN INFANTS AND CHILDREN WITH CONGENITAL ADRENAL HYPERPLASIA SUGGESTING DIFFERENT 21-HYDROXYLATION DEFECTS IN "SALT-LOSERS" AND "NON SALT-LOSERS". Acta Endocrinol (Copenh) 1965 Apr;48:587–601. doi: 10.1530/acta.0.0480587. [DOI] [PubMed] [Google Scholar]
  3. Godard C., Riondel A. M., Veyrat R., Mégevand A., Muller A. F. Plasma renin activity and aldosterone secretion in congenital adrenal hyperplasia. Pediatrics. 1968 May;41(5):883–904. [PubMed] [Google Scholar]
  4. New M. I., Miller B., Peterson R. E. Aldosterone excretion in normal children and in children with adrenal hyperplasia. J Clin Invest. 1966 Mar;45(3):412–428. doi: 10.1172/JCI105356. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. VISSER H. K., COST W. S. A NEW HEREDITARY DEFECT IN THE BIOSYNTHESIS OF ALDOSTERONE: URINARY C21-CORTICOSTEROID PATTERN IN THREE RELATED PATIENTS WITH A SALT-LOSING SYNDROME, SUGGESTING AN 18-OXIDATION DEFECT. Acta Endocrinol (Copenh) 1964 Dec;47:589–612. doi: 10.1530/acta.0.0470589. [DOI] [PubMed] [Google Scholar]

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