These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

102 related items for PubMed ID: 6270940

  • 1. 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]

  • 2. 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]

  • 3. 17 alpha-hydroxylase deficiency syndrome associated with bilateral streak gonads and impaired development of Müllerian ducts derivatives. Report of a case.
    de Gennes JL, Jambart S, Turpin G, Elkik F, Roger M.
    Acta Endocrinol (Copenh); 1982 May; 100(1):68-76. PubMed ID: 6287777
    [Abstract] [Full Text] [Related]

  • 4. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 5. Severe hypertension with absent secondary sex characteristics due to partial deficiency of steroid 17 alpha-hydroxylase activity.
    Fraser R, Brown JJ, Mason PA, Morton JJ, Lever AF, Robertson JI, Lee HA, Miller H.
    J Hum Hypertens; 1987 Jun 07; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 6. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    Yanase E, Nagai T, Kato M, Morimoto S.
    Jpn J Med; 1982 Apr 07; 21(2):128-34. PubMed ID: 6750188
    [Abstract] [Full Text] [Related]

  • 7. 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 07; 36(4):515-36. PubMed ID: 2555148
    [Abstract] [Full Text] [Related]

  • 8. 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 Aug 07; 13(2):98-108. PubMed ID: 6262207
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase.
    Roger M, Merceron RE, Girard F, Canlorbe P, Dehennin L, Konopka P, Seneze J, Toublanc JE.
    Horm Res; 1982 Aug 07; 16(1):23-31. PubMed ID: 6279481
    [Abstract] [Full Text] [Related]

  • 11. A new variant of 17 alpha-hydroxylase deficiency with hyperaldosteronism in two Japanese sisters.
    Monno S, Takasu N.
    Endocrinol Jpn; 1989 Apr 07; 36(2):315-23. PubMed ID: 2550210
    [Abstract] [Full Text] [Related]

  • 12. 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 07; 14(2):99-108. PubMed ID: 1648117
    [Abstract] [Full Text] [Related]

  • 13. New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasia.
    Levine LS, Rauh W, Gottesdiener K, Chow D, Gunczler P, Rapaport R, Pang S, Schneider B, New MI.
    J Clin Endocrinol Metab; 1980 Feb 07; 50(2):258-63. PubMed ID: 6243663
    [Abstract] [Full Text] [Related]

  • 14. Dissociation of plasma renin activity and plasma aldosterone level during dexamethasone suppression test in non-salt-losers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Kinoshita K, Ishida H, Minowada S, Niijima T.
    Endocrinol Jpn; 1980 Dec 07; 27(6):747-51. PubMed ID: 7021135
    [Abstract] [Full Text] [Related]

  • 15. 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 07; 56(4):697-701. PubMed ID: 6300162
    [Abstract] [Full Text] [Related]

  • 16. Hypertension due to 17alpha-hydroxylase deficiency.
    Wang C, Yeung RT, Coghlan JP, Oddie CJ, Scoggins BA, Stockigt JR.
    Aust N Z J Med; 1978 Jun 07; 8(3):295-9. PubMed ID: 308800
    [Abstract] [Full Text] [Related]

  • 17. [A case of glucocorticoid-responsive hyperaldosteronism: follow-up study for 21 years--comparison with cases of 17 alpha-hydroxylase deficiency in Japan].
    Murase H, Yamakita N, Yasuda K, Noritake N, Mercado-Asis LB, Takeuchi K, Murakami O, Abe K, Yoshinaga K, Miura K.
    Nihon Naibunpi Gakkai Zasshi; 1990 Jan 20; 66(1):50-82. PubMed ID: 2407572
    [Abstract] [Full Text] [Related]

  • 18. A case of 17 alpha-hydroxylase deficiency syndrome associated with right adrenal tumor.
    Ogawa K, Hara A, Tanabe S, Tamori S, Yoshida H, Pak CH, Matsunaga M, Kawai C, Dodo H, Tanimura H.
    Clin Exp Hypertens A; 1984 Jan 20; 6(4):863-77. PubMed ID: 6609788
    [Abstract] [Full Text] [Related]

  • 19. 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 20; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

  • 20. The unique patterns of plasma aldosterone and 18-hydroxycorticosterone concentrations in the 17 alpha-hydroxylase deficiency syndrome.
    Kater CE, Biglieri EG, Brust N, Chang B, Hirai J.
    J Clin Endocrinol Metab; 1982 Aug 20; 55(2):295-302. PubMed ID: 7045152
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.