Medical and Psychological Management of Congenital Adrenal Hyperplasia
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Publisher
Springer Netherlands
Link
http://link.springer.com/content/pdf/10.1007/978-94-009-5610-0_6
Reference80 articles.
1. Hughes, I.A. (1982). Congenital and acquired disorders of the adrenal cortex. Clin. Endocrinol. (Oxf.), 11, 89–125
2. Strott, C. A., Yoshimi, T. and Lipsett, M. B. (1969). Plasma progesterone and 17-hydroxyprogesterone in normal men and children with congenital adrenal hyperplasia. J. Clin. Invest., 48, 930–939
3. Horton, R. and Frasier, S. D. (1967). Androstenedione and its conversion to plasma testosterone in congenital adrenal hyperplasia. J. Clin. Invest., 46, 1003–1009
4. Fife, D. and Rappaport, E. B. (1983). Prevalence of salt-losing among congenital adrenal hyperplasia patients. Clin. Endocrinol. (Oxf.), 19, 259–264
5. Ulick, S., Eberlin, W. R., Bliffeld, A. R., Chu, M. D. and Bongiovanni, A. M. (1980). Evidence for an aldosterone biosynthetic defect in congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab., 51, 1346–1353
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1. Muscle Strength in Girls with Congenital Adrenal Hyperplasia;Acta Paediatrica;1987-05
2. Radioimmunoassay of Blood-Spot 17α-Hydroxyprogesterone in the Management of Congenital Adrenal Hyperplasia;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;1987-01
3. Clinical aspects of congenital adrenal hyperplasia: Early diagnosis and prognosis;Journal of Inherited Metabolic Disease;1986-03
4. Clinical Aspects of Congenital Adrenal Hyperplasia: Early Diagnosis and Prognosis;Practical Developments in Inherited Metabolic Disease: DNA Analysis, Phenylketonuria and Screening for Congenital Adrenal Hyperplasia;1986
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