Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/BF03349283.pdf
Reference58 articles.
1. Bongiovanni A.M., Eberlein W.R. Defective steroidal biogenesis in congenital adrenal hyperplasia. Pediatrics 21: 661,1958.
2. Bongiovanni A.M., Root A.W. The adrenogenital syndrome. N. Engl. J. Med. 268: 1283, 1342, and 1391, 1963.
3. New M.I., Miller B., Peterson R.E. Aldosterone excretion in normal children, and in children with adrenal hyperplasia. J. Clin. Invest. 45:412, 1966.
4. Simopoulos A.P., Marshall J.R., Delea C.S., Bartter F.C. Studies on the deficiency of 21-hydroxylation in patients with congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab. 32: 438, 1971.
5. Beitins I.Z., Bayard F., Kowarski A., Migeon C.J. The effect of ACTH administration on aldosterone production in non salt-losing congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab. 34: 595, 1972.
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