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Journal Abstract Search

662 related items for PubMed ID: 2932643

  • 1. 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]

  • 2. 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]

  • 3. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism.
    Siegel SF, Finegold DN, Lanes R, Lee PA.
    N Engl J Med; 1990 Sep 27; 323(13):849-54. PubMed ID: 2168515
    [Abstract] [Full Text] [Related]

  • 4. Six-month oral dehydroepiandrosterone supplementation in early and late postmenopause.
    Stomati M, Monteleone P, Casarosa E, Quirici B, Puccetti S, Bernardi F, Genazzani AD, Rovati L, Luisi M, Genazzani AR.
    Gynecol Endocrinol; 2000 Oct 27; 14(5):342-63. PubMed ID: 11109974
    [Abstract] [Full Text] [Related]

  • 5. Familial male pseudohermaphroditism due to 17-20-desmolase deficiency. I. In vivo endocrine studies.
    Forest MG, Lecornu M, de Peretti E.
    J Clin Endocrinol Metab; 1980 May 27; 50(5):826-33. PubMed ID: 6246133
    [Abstract] [Full Text] [Related]

  • 6. Pregnenolone, 17-OH-pregnenolone, and testosterone in plasma of patients with congenital adrenal hyperplasia.
    McKenna TJ, Jennings AS, Liddle GW, Burr IM.
    J Clin Endocrinol Metab; 1976 May 27; 42(5):918-25. PubMed ID: 178685
    [Abstract] [Full Text] [Related]

  • 7. 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 27; 75(1):43-8. PubMed ID: 6602548
    [Abstract] [Full Text] [Related]

  • 8. Partial 17, 20-desmolase and 17 alpha-hydroxylase deficiencies in a 16-year-old boy.
    Bosson D, Wolter R, Toppet M, Franckson JR, de Peretti E, Forest MG.
    J Endocrinol Invest; 1988 Jul 27; 11(7):527-33. PubMed ID: 3139743
    [Abstract] [Full Text] [Related]

  • 9. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Jul 27; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 10. 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 27; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 11. Diagnosis of congenital adrenal hyperplasia with 11-hydroxylase deficiency by determination of tetrahydro-11-desoxycortisol in urine.
    Knorr D, Bidlingmaier F.
    Helv Paediatr Acta; 1974 Feb 27; Suppl 34():119-25. PubMed ID: 4452634
    [No Abstract] [Full Text] [Related]

  • 12. 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 27; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

  • 13. 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 27; 55(2):295-302. PubMed ID: 7045152
    [No Abstract] [Full Text] [Related]

  • 14. [Defects of adrenal steroidogenesis in patients with hirsutism].
    Salinas Vert I, Audí Parera L, Granada Ybern ML, Lucas Martín A, Pizarro Lozano E, Foz Sala M, Sanmartí Sala A.
    Med Clin (Barc); 1998 Feb 14; 110(5):171-6. PubMed ID: 9547720
    [Abstract] [Full Text] [Related]

  • 15. [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 14; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 16. In vivo and in vitro studies in a 46, XY phenotypically female infant with 17-ketosteroid reductase deficiency.
    Wit JM, van Hooff CO, Thijssen JH, Van den Brande JL.
    Horm Metab Res; 1988 Jun 14; 20(6):367-74. PubMed ID: 2971011
    [Abstract] [Full Text] [Related]

  • 17. Cortisol, aldosterone, cortisol precursor, androgen and endogenous ACTH concentrations in dogs with pituitary-dependant hyperadrenocorticism treated with trilostane.
    Sieber-Ruckstuhl NS, Boretti FS, Wenger M, Maser-Gluth C, Reusch CE.
    Domest Anim Endocrinol; 2006 Jul 14; 31(1):63-75. PubMed ID: 16233969
    [Abstract] [Full Text] [Related]

  • 18. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Jul 14; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 19. Molecular characterization of a Leydig cell tumor presenting as congenital adrenal hyperplasia.
    Solish SB, Goldsmith MA, Voutilainen R, Miller WL.
    J Clin Endocrinol Metab; 1989 Dec 14; 69(6):1148-52. PubMed ID: 2555382
    [Abstract] [Full Text] [Related]

  • 20. Metabolism and concentration of androgenic steroids in abdominal skin of hirsute women with androgenital syndrome.
    Tóth I, Faredin I.
    Acta Med Hung; 1984 Dec 14; 41(1):7-18. PubMed ID: 6234510
    [Abstract] [Full Text] [Related]

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