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22. [Primary hypoaldosteronism caused by a probable anomaly of 18-hydroxylation]. Jean R; Legrand JC; Meylan F; Rieu D; Astruc J Arch Fr Pediatr; 1969; 26(7):769-77. PubMed ID: 5355252 [No Abstract] [Full Text] [Related]
23. [11-beta-hydroxylase deficiency and glucocorticoid-sensitive hyperaldosteronism]. Merino Arribas JM; Rámila de la Torre E; Sánchez Martín J; Avellanosa Arnaiz A; González de la Rosa JB An Esp Pediatr; 1996 Jun; 44(6):609-11. PubMed ID: 8849112 [No Abstract] [Full Text] [Related]
24. [Juxtaglomerular cells in the virilizing congenital adrenogenital syndrome, with and without the salt-loss syndrome]. Osterwalder H Schweiz Med Wochenschr; 1971 Sep; 101(36):1298-305. PubMed ID: 5141785 [No Abstract] [Full Text] [Related]
25. A new form of congenital adrenal hyperplasia. New MI; Peterson RE J Clin Endocrinol Metab; 1967 Feb; 27(2):300-5. PubMed ID: 6018580 [No Abstract] [Full Text] [Related]
26. [Case report on a female patient with 17- -hydroxylase deficiency]. Gassel WD; Gerdes H; Littmann KP Verh Dtsch Ges Inn Med; 1971; 77():1057-60. PubMed ID: 4346174 [No Abstract] [Full Text] [Related]
27. [Pregnantriolon excretion after ACTH-stimulation in possible heterocygotes of 21-hydroxylase deficiency (author's transl)]. Gleispach H; Berger H; Glatzl J; Rössler H; Tschager E Padiatr Padol; 1971; 6(3):287-96. PubMed ID: 4363023 [No Abstract] [Full Text] [Related]
28. Biochemical diagnosis and management of corticosterone methyl oxidase type II deficiency. Lee PD; Patterson BD; Hintz RL; Rosenfeld RG J Clin Endocrinol Metab; 1986 Jan; 62(1):225-9. PubMed ID: 3510001 [TBL] [Abstract][Full Text] [Related]
29. [Adrenal insufficiency due to enzyme deficiency]. Shimizu N Saishin Igaku; 1970 Mar; 25(3):548-52. PubMed ID: 4912570 [No Abstract] [Full Text] [Related]