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150 related items for PubMed ID: 1648117
1. 17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies. Scaroni C, Biason A, Carpenè G, Opocher G, Mantero F. J Endocrinol Invest; 1991 Feb; 14(2):99-108. PubMed ID: 1648117 [Abstract] [Full Text] [Related]
2. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia. Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A. J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904 [Abstract] [Full Text] [Related]
3. 17 alpha-hydroxylase deficiency: mineralocorticoid hormone profiles in an affected family. D'Armiento M, Reda G, Kater C, Shackleton CH, Biglieri EG. J Clin Endocrinol Metab; 1983 Apr; 56(4):697-701. PubMed ID: 6300162 [Abstract] [Full Text] [Related]
4. Possible hyperaldosteronism and discrepancy in enzyme activity deficiency in adrenal and gonadal glands in Japanese patients with 17 alpha-hydroxylase deficiency. Yamakita N, Murase H, Yasuda K, Noritake N, Mercado-Asis LB, Miura K. Endocrinol Jpn; 1989 Aug; 36(4):515-36. PubMed ID: 2555148 [Abstract] [Full Text] [Related]
5. Diagnosis and treatment of 17-hydroxylase deficiency. Peter M, Sippell WG, Wernze H. J Steroid Biochem Mol Biol; 1993 Apr; 45(1-3):107-16. PubMed ID: 8481334 [Abstract] [Full Text] [Related]
6. Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function. Pang S, Levine LS, Stoner E, Opitz JM, Pollack MS, Dupont B, New MI. J Clin Endocrinol Metab; 1983 Apr; 56(4):808-18. PubMed ID: 6300166 [Abstract] [Full Text] [Related]
7. 17 alpha-Hydroxylase deficiency. A combination of hydroxylation defect and reversible blockade in aldosterone biosynthesis. Rovner DR, Conn JW, Cohen EL, Berlinger FG, Kem DC, Gordon DL. Acta Endocrinol (Copenh); 1979 Mar; 90(3):490-504. PubMed ID: 218415 [Abstract] [Full Text] [Related]
8. HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS). Scaroni C, Orlandini E, Venturi Pasini C, Gangemi M, Mantero F. J Endocrinol Invest; 1986 Feb; 9(1):65-70. PubMed ID: 3009598 [Abstract] [Full Text] [Related]
9. Siblings of 21-hydroxylase deficiency (non-salt-losing) with aldosterone hypersecretion. Morimoto I, Yamamoto S, Tateishi H, Ueda S, Toda Y, Zeki K, Watanabe K, Nakano Y, Kashimura M, Eto S. Intern Med; 1992 May; 31(5):690-4. PubMed ID: 1324037 [Abstract] [Full Text] [Related]
10. [Congenital adrenal hyperplasia]. Stanić M, Nesović M. Med Pregl; 1999 May; 52(11-12):447-54. PubMed ID: 10748766 [Abstract] [Full Text] [Related]
11. Effect of carbenoxolone on the plasma renin activity and hypothalamic-pituitary-adrenal axis in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Irony I, Cutler GB. Clin Endocrinol (Oxf); 1999 Sep; 51(3):285-91. PubMed ID: 10469007 [Abstract] [Full Text] [Related]
12. Two cases of 17 alpha-hydroxylase deficiency--one combined with complete gonadal agenesis. Tvedegaard E, Frederiksen V, Olgaard K, Nielsen MD, Starup J. Acta Endocrinol (Copenh); 1981 Oct; 98(2):267-73. PubMed ID: 6270940 [Abstract] [Full Text] [Related]
13. Control of aldosterone in 17 alpha-hydroxylase deficiency. Saruta T, Kondo K, Saito I, Nagahama S, Suzuki H, Konishi K, Matsuki S. Horm Res; 1980 Oct; 13(2):98-108. PubMed ID: 6262207 [Abstract] [Full Text] [Related]
14. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency and hormonal profiles in the nuclear family. Rohmer V, Barbot N, Bertrand P, Nahoul K, Bigorgne JC, Forest MG. J Clin Endocrinol Metab; 1990 Aug; 71(2):523-9. PubMed ID: 2166072 [Abstract] [Full Text] [Related]
15. An autopsy case of 17 alpha-hydroxylase deficiency with malignant hypertension. Morimoto I, Maeda R, Izumi M, Ishimaru T, Nishimori I, Nagataki S. J Clin Endocrinol Metab; 1983 May; 56(5):915-9. PubMed ID: 6300176 [Abstract] [Full Text] [Related]