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4. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency]. Liotta A; Cammarata M; Corsello G; Ferrara D; Giuffrè L Pediatr Med Chir; 1987; 9(3):309-10. PubMed ID: 2823235 [TBL] [Abstract][Full Text] [Related]
5. [Congenital adrenal hyperplasia due to 3beta-hydroxysteroid dehydrogenase deficiency]. Marunová M Vnitr Lek; 2006 Oct; 52(10):957-62. PubMed ID: 17063810 [TBL] [Abstract][Full Text] [Related]
6. [Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature]. De Marinis L; Mancini A; Saporosi A; Calabrò F; Massari M; Moneta E; Menini E; Barbarino A Minerva Ginecol; 1989 Jul; 41(7):337-42. PubMed ID: 2691923 [TBL] [Abstract][Full Text] [Related]
7. Congenital adrenal hyperplasia. Savage MO Clin Endocrinol Metab; 1985 Nov; 14(4):893-909. PubMed ID: 3910306 [No Abstract] [Full Text] [Related]
8. A female pseudohermaphrodite with salt losing congenital adrenal hyperplasia as the result of 21--beta--OH deficiency. Preeyasombat C; Siripoonya P; Tejavej A; Pitchayayothin N J Med Assoc Thai; 1975 Mar; 58(3):61-9. PubMed ID: 1127377 [No Abstract] [Full Text] [Related]
9. [Genetics and endocrinology of male sex differentiation: application to molecular study of male pseudohermaphroditism]. Sultan C; Lumbroso S; Poujol N; Boudon C; Georget V; Térouanne B; Belon C; Lobaccaro JM C R Seances Soc Biol Fil; 1995; 189(5):713-40. PubMed ID: 8673622 [TBL] [Abstract][Full Text] [Related]
10. Congenital adrenal hyperplasia owing to 3 beta-hydroxysteroid dehydrogenase deficiency. Pang S Endocrinol Metab Clin North Am; 2001 Mar; 30(1):81-99, vi-vii. PubMed ID: 11344940 [TBL] [Abstract][Full Text] [Related]
11. [Report on 3 cases of 17 alpha-hydroxylase deficiency]. Zhang ZJ Zhonghua Nei Ke Za Zhi; 1983 Sep; 22(9):565-7. PubMed ID: 6606541 [No Abstract] [Full Text] [Related]
12. A case of late-onset congenital adrenal hyperplasia due to partial 3 beta-hydroxysteroid dehydrogenase deficiency. Hattori N; Ishihara T; Moridera K; Hino M; Ikekubo K; Kurahachi H Endocr J; 1993 Feb; 40(1):107-9. PubMed ID: 7951484 [TBL] [Abstract][Full Text] [Related]
13. [Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood]. Mackenroth T Internist (Berl); 1986 Apr; 27(4):274-8. PubMed ID: 3519519 [No Abstract] [Full Text] [Related]
14. [Congenital adrenogenital syndrome due to 21-hydroxylase deficiency. Pathogenesis, clinical picture, and deliberations over better therapy]. von Schnakenburg K Med Welt; 1977 Sep; 28(36):1415-22. PubMed ID: 904447 [No Abstract] [Full Text] [Related]
15. A genetic male patient with 17 alpha-hydroxylase deficiency. Jones HW; Lee PA; Rock JA; Archer DF; Migeon CJ Obstet Gynecol; 1982 Feb; 59(2):254-9. PubMed ID: 6979016 [TBL] [Abstract][Full Text] [Related]
16. Male pseudohermaphroditism caused by nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency. Heinrich UE; Bettendorf M; Vecsei P J Steroid Biochem Mol Biol; 1993 Apr; 45(1-3):83-5. PubMed ID: 8481355 [TBL] [Abstract][Full Text] [Related]
17. Congenital adrenal hyperplasia. Molecular insights learned from patients. Kalaitzoglou G; New MI Receptor; 1993; 3(3):211-22. PubMed ID: 8167572 [TBL] [Abstract][Full Text] [Related]