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2. Neonatal screening for 21-hydroxylase deficiency: a microfilter paper method for 17-alpha-hydroxyprogesterone assay. Piazzi S, Capelli M, Paolini M, Perugini D, Grossi G, Balsamo A, Salomoni P, Cassio A, Bugiardini G, Cacciari E. J Endocrinol Invest; 1982; 5(2):87-90. PubMed ID: 6980238 [Abstract] [Full Text] [Related]
3. [Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 3. An enzyme-linked immunosorbent assay for dried blood 17 alpha-hydroxyprogesterone]. Fukushi M, Arai O, Mizushima Y, Takasugi N, Fujieda K, Matsuura N. Nihon Naibunpi Gakkai Zasshi; 1987 Feb 20; 63(2):113-22. PubMed ID: 3494638 [Abstract] [Full Text] [Related]
8. [Neonatal mass-screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. I. Microfilter paper methods for radioimmunoassay of 17 alpha-hydroxyprogesterone]. Shimozawa K. Nihon Naibunpi Gakkai Zasshi; 1983 Dec 20; 59(12):1845-9. PubMed ID: 6609091 [Abstract] [Full Text] [Related]
16. [Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 2. Analysis of steroids with high-performance liquid chromatography for diagnosis of congenital adrenal hyperplasia]. Mizushima Y, Fukushi M, Arai O, Takasugi N, Fujieda K, Matsuura N, Fujimoto S. Nihon Naibunpi Gakkai Zasshi; 1987 Feb 20; 63(2):102-12. PubMed ID: 3494637 [Abstract] [Full Text] [Related]
19. A method for identification and follow-up of patients with a steroid-21-hydroxylase deficiency. Sólyom J, Hammond GL, Vihko R. Clin Chim Acta; 1979 Mar 01; 92(2):117-24. PubMed ID: 314867 [Abstract] [Full Text] [Related]