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Journal Abstract Search

94 related items for PubMed ID: 3091739

  • 1. [A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency with high levels of plasma aldosterone and angiotensin II].
    Toyoda N, Murata K, Tanaka Y, Kawai Y, Yamamoto T, Nishiyama Y, Matsumoto T, Sugiyama Y.
    Nihon Sanka Fujinka Gakkai Zasshi; 1986 Jul; 38(7):1162-5. PubMed ID: 3091739
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [17 alpha-hydroxylase deficiency and 5 alpha-reductase deficiency].
    Yoshida H, Shimizu N.
    Nihon Rinsho; 1979 Jun 10; 37(6):1253-9. PubMed ID: 384051
    [No Abstract] [Full Text] [Related]

  • 4. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
    Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L.
    Pediatr Med Chir; 1987 Jun 10; 9(3):309-10. PubMed ID: 2823235
    [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 10; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 6. 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 Jun 10; 13(2):98-108. PubMed ID: 6262207
    [Abstract] [Full Text] [Related]

  • 7. [Partial deficiency in 21-hydroxylase in certain forms of hirsutism].
    Lucisano A, Satta MA, Tripodi R, Mobili L, De Cicco F, Monaco F, Dell'Acqua S, Roche J.
    C R Seances Soc Biol Fil; 1989 Jun 10; 183(2):117-21. PubMed ID: 2555033
    [Abstract] [Full Text] [Related]

  • 8. Mechanisms establishing the mineralocorticoid hormone patterns in the 17 alpha-hydroxylase deficiency syndrome.
    Biglieri EG.
    J Steroid Biochem; 1979 Jul 10; 11(1B):653-7. PubMed ID: 226795
    [No Abstract] [Full Text] [Related]

  • 9. Gynecomastia with congenital virilizing adrenal hyperplasia (11-beta-hydroxylase deficiency).
    Maclaren NK, Migeon CJ, Raiti S.
    J Pediatr; 1975 Apr 10; 86(4):579-81. PubMed ID: 123956
    [No Abstract] [Full Text] [Related]

  • 10. 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 10; 55(2):295-302. PubMed ID: 7045152
    [No Abstract] [Full Text] [Related]

  • 11. 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 10; 56(4):697-701. PubMed ID: 6300162
    [Abstract] [Full Text] [Related]

  • 12. Angiotensin and adrenal steroidogenesis: study of 21-hydroxylase-deficient congenital adrenal hyperplasia.
    Schaison G, Couzinet B, Gourmelen M, Elkik F, Bougneres P.
    J Clin Endocrinol Metab; 1980 Dec 10; 51(6):1390-4. PubMed ID: 7002950
    [Abstract] [Full Text] [Related]

  • 13. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar 10; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 14. [Malignant arterial hypertension disclosing late congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency].
    Ribstein J, Sciolla JP, Barjon P, Sultan C, Forest M, de Peretti E.
    Arch Mal Coeur Vaiss; 1988 Jun 10; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 15. [A case of a simple virilizing form of 21-hydroxylase deficiency with schizophrenic symptoms, marked pigmentation and highly elevated plasma deoxycorticosterone].
    Suemaru S, Hashimoto K, Hattori T, Inoue H, Kageyama J, Ota Z.
    Nihon Naika Gakkai Zasshi; 1987 Jan 10; 76(1):112-7. PubMed ID: 3033104
    [No Abstract] [Full Text] [Related]

  • 16. 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 10; 71(2):523-9. PubMed ID: 2166072
    [Abstract] [Full Text] [Related]

  • 17. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
    Waldhäusl W, Herkner K, Nowotny P, Bratusch-Marrain P.
    J Clin Endocrinol Metab; 1978 Feb 10; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 18. Distinctive plasma aldosterone, 18-hydroxycorticosterone, and 18-hydroxydeoxycorticosterone profile in the 21-, 17 alpha-, and 11 beta-hydroxylase deficiency types of congenital adrenal hyperplasia.
    Kater CE, Biglieri EG.
    Am J Med; 1983 Jul 10; 75(1):43-8. PubMed ID: 6602548
    [Abstract] [Full Text] [Related]

  • 19. 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 10; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 20. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 10; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

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