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Journal Abstract Search

143 related items for PubMed ID: 384051

  • 21. Urinary steroid metabolites in subjects with male pseudohermaphroditism due to 5 alpha-reductase deficiency.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    Clin Endocrinol (Oxf); 1985 Jul; 23(1):43-53. PubMed ID: 4028464
    [Abstract] [Full Text] [Related]

  • 22. Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. A study of five cases.
    Bouchard P, Kuttenn F, Mowszowicz I, Schaison G, Raux-Eurin MC, Mauvais-Jarvis P.
    Acta Endocrinol (Copenh); 1981 Jan; 96(1):107-11. PubMed ID: 6257014
    [No Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Decreased urinary C19 and C21 steroid 5 alpha-metabolites in parents of male pseudohermaphrodites with 5 alpha-reductase deficiency: detection of carriers.
    Imperato-McGinley J, Peterson RE, Gautier T, Arthur A, Shackleton C.
    J Clin Endocrinol Metab; 1985 Mar; 60(3):553-8. PubMed ID: 3972966
    [Abstract] [Full Text] [Related]

  • 25. [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]

  • 26. Prepubertal diagnosis of steroid 5 alpha-reductase deficiency.
    Saenger P, Goldman AS, Levine LS, Korth-Schutz S, Muecke EC, Katsumata M, Doberne Y, New MI.
    J Clin Endocrinol Metab; 1978 Apr; 46(4):627-34. PubMed ID: 755047
    [Abstract] [Full Text] [Related]

  • 27. [17 alpha-hydroxylase deficiency].
    Kumagi R.
    Nihon Rinsho; 1977 Apr; 35 Suppl 1():1096-7. PubMed ID: 306453
    [No Abstract] [Full Text] [Related]

  • 28. [Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. A clinical case].
    Zacharías S, Contreras P.
    Rev Chil Obstet Ginecol; 1984 Apr; 49(5):295-9. PubMed ID: 6242254
    [No Abstract] [Full Text] [Related]

  • 29. 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]

  • 30. 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; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 31. 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]

  • 32. 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 May; 22(6):191-4. PubMed ID: 316501
    [No Abstract] [Full Text] [Related]

  • 33. Diagnosis and management of the infant with genital ambiguity.
    Simpson JL.
    Am J Obstet Gynecol; 1977 May 15; 128(2):137-45. PubMed ID: 855867
    [Abstract] [Full Text] [Related]

  • 34. The prevalence of 5 alpha-reductase deficiency in children with ambiguous genitalia in the Dominican Republic.
    Imperato-McGinley J, Gautier T, Peterson RE, Shackleton C.
    J Urol; 1986 Oct 15; 136(4):867-73. PubMed ID: 3489839
    [Abstract] [Full Text] [Related]

  • 35. 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 Oct 15; 91():416-23. PubMed ID: 224555
    [No Abstract] [Full Text] [Related]

  • 36. [Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature].
    De Marinis L, Mancini A, Saporosi A, Calabrò F, Massari M, Moneta E, Menini E, Barbarino A.
    Minerva Ginecol; 1989 Jul 15; 41(7):337-42. PubMed ID: 2691923
    [Abstract] [Full Text] [Related]

  • 37. 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 15; 1(1):53-8. PubMed ID: 2854163
    [Abstract] [Full Text] [Related]

  • 38. 5 alpha-reductase deficiency in humans: support to the theory that 5 alpha-reduction of testosterone is an essential step in the control of LH secretion.
    Martini L, Celotti F, Serio M.
    J Endocrinol Invest; 1979 Jun 15; 2(4):463-4. PubMed ID: 536582
    [No Abstract] [Full Text] [Related]

  • 39. Steroid 5 alpha-reductase 2 deficiency.
    Wilson JD, Griffin JE, Russell DW.
    Endocr Rev; 1993 Oct 15; 14(5):577-93. PubMed ID: 8262007
    [Abstract] [Full Text] [Related]

  • 40. Familial male pseudohermaphroditism due to deficiency of 5 alpha-reductase.
    Savage MO, Preece MA, Jeffcoate SL, Ransley PG, Rumsby G, Mansfield MD, Williams DI.
    Clin Endocrinol (Oxf); 1980 Apr 15; 12(4):397-406. PubMed ID: 7379320
    [Abstract] [Full Text] [Related]

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