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Journal Abstract Search

66 related items for PubMed ID: 224555

  • 1. Direct evidence for a functional block in 18 oxidation in a patient with 17 alpha hydroxylase deficiency.
    Rovner DR, Gordon DL, Swisher SN.
    Trans Assoc Am Physicians; 1978; 91():416-23. PubMed ID: 224555
    [No Abstract] [Full Text] [Related]

  • 2. 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; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 3. Requirement of mineralocorticoid in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Hochberg Z, Benderly A, Kahana L, Zadik Z.
    J Clin Endocrinol Metab; 1986 Jul; 63(1):36-40. PubMed ID: 3011843
    [Abstract] [Full Text] [Related]

  • 4. Failure of angiotensin II to stimulate increases in concentrations of adrenal androgens, 17-hydroxyprogesterone, or adrenocorticotropin in congenital 21-hydroxylase deficiency.
    Wisgerhof M, Mellinger RC, Zafar MS.
    J Clin Endocrinol Metab; 1983 Mar; 56(3):627-31. PubMed ID: 6296191
    [Abstract] [Full Text] [Related]

  • 5. [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; 76(1):112-7. PubMed ID: 3033104
    [No Abstract] [Full Text] [Related]

  • 6. Incomplete virilization and subclinical mineralocorticoid excess in a boy with partial 17,20-desmolase/17 alpha-hydroxylase deficiency.
    de Lange WE, Doorenbos H.
    Acta Endocrinol (Copenh); 1990 Feb; 122(2):263-6. PubMed ID: 2156398
    [Abstract] [Full Text] [Related]

  • 7. Variable efficacy of glucocorticoids in congenital adrenal hyperplasia.
    Hansen JW, Loriaux DL.
    Pediatrics; 1976 Jun; 57(6):942-7. PubMed ID: 934750
    [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; 11(1B):653-7. PubMed ID: 226795
    [No Abstract] [Full Text] [Related]

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

  • 10. [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; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 11. Late onset adrenocortical hydroxylase deficiencies associated with menstrual dysfunction.
    Birnbaum MD, Rose LI.
    Obstet Gynecol; 1984 Apr; 63(4):445-51. PubMed ID: 6322077
    [Abstract] [Full Text] [Related]

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

  • 13. [Congenital virilization in a newborn girl of a mother with adrenogenital syndrome due to 21-hydroxylase deficiency].
    Ferrante L.
    Minerva Pediatr; 1976 Jun 23; 28(22):1443-4. PubMed ID: 986003
    [No Abstract] [Full Text] [Related]

  • 14. Steroid spectrum in human urine as revealed by gas chromatography. IV. Changes in the exception of 16-oxygenated neutral steroids by children with 21-hydroxylase deficiency during different stages of development.
    Kecskés L, Juricskay Z, Kosztoláni G, Szécsényi M.
    Acta Biochim Biophys Acad Sci Hung; 1981 Jun 23; 16(1-2):57-75. PubMed ID: 6278806
    [No Abstract] [Full Text] [Related]

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

  • 16. [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 23; 38(7):1162-5. PubMed ID: 3091739
    [No Abstract] [Full Text] [Related]

  • 17. [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]

  • 18. [Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood].
    Mackenroth T.
    Internist (Berl); 1986 Apr 10; 27(4):274-8. PubMed ID: 3519519
    [No Abstract] [Full Text] [Related]

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

  • 20. Primary adrenal insufficiency with hypertension. A case report on partial primary adrenal insufficiency and partial 11-beta-hydroxylase deficiency.
    van Deijk WA, Blom PS, VD Vijver JC.
    Neth J Med; 1979 Apr 10; 22(6):191-4. PubMed ID: 316501
    [No Abstract] [Full Text] [Related]

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