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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]

  • 16. Dexamethasone-suppressible hyperaldosteronism. Adrenal transition cell hyperplasia?
    Connell JM, Kenyon CJ, Corrie JE, Fraser R, Watt R, Lever AF.
    Hypertension; 1986 Aug; 8(8):669-76. PubMed ID: 3015796
    [Abstract] [Full Text] [Related]

  • 17. Impaired mineralocorticoid hormone responses to adrenocorticotropin stimulation: additional characterization of heterozygosity for the 21-hydroxylase deficiency type of congenital adrenal hyperplasia.
    Pardini DP, Kater CE, Vieira JG, Biglieri EG.
    J Clin Endocrinol Metab; 1983 Nov; 57(5):1061-6. PubMed ID: 6311859
    [Abstract] [Full Text] [Related]

  • 18. Testicular adrenal rests: evidence for luteinizing hormone receptors and for distinct types of testicular nodules differing for their autonomization.
    Benvenga S, Smedile G, Lo Giudice F, Trimarchi F.
    Eur J Endocrinol; 1999 Sep; 141(3):231-7. PubMed ID: 10474120
    [Abstract] [Full Text] [Related]

  • 19. Hypothalamic-pituitary-gonadal axis function in pubertal male and female siblings with glucocorticoid-treated nonsalt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia.
    Chang YT, Kulin HE, Garibaldi L, Suriano MJ, Bracki K, Pang S.
    J Clin Endocrinol Metab; 1993 Nov; 77(5):1251-7. PubMed ID: 8077318
    [Abstract] [Full Text] [Related]

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