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Journal Abstract Search

161 related items for PubMed ID: 6314235

  • 1. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.
    Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF.
    Pediatrics; 1983 Nov; 72(5):690-5. PubMed ID: 6314235
    [Abstract] [Full Text] [Related]

  • 2. Late-onset adrenal hyperplasia in hirsutism.
    Kuttenn F, Couillin P, Girard F, Billaud L, Vincens M, Boucekkine C, Thalabard JC, Maudelonde T, Spritzer P, Mowszowicz I.
    N Engl J Med; 1985 Jul 25; 313(4):224-31. PubMed ID: 2989686
    [Abstract] [Full Text] [Related]

  • 3. The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women.
    Chetkowski RJ, DeFazio J, Shamonki I, Judd HL, Chang RJ.
    J Clin Endocrinol Metab; 1984 Apr 25; 58(4):595-8. PubMed ID: 6321532
    [Abstract] [Full Text] [Related]

  • 4. Dexamethasone preparation does not alter corticoid and androgen responses to adrenocorticotropin.
    Rosenfield RL, Helke J, Lucky AW.
    J Clin Endocrinol Metab; 1985 Mar 25; 60(3):585-9. PubMed ID: 2982902
    [Abstract] [Full Text] [Related]

  • 5. [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 Mar 25; 183(2):117-21. PubMed ID: 2555033
    [Abstract] [Full Text] [Related]

  • 6. Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.
    Lobo RA, Goebelsmann U.
    Am J Obstet Gynecol; 1980 Nov 15; 138(6):720-6. PubMed ID: 6254362
    [Abstract] [Full Text] [Related]

  • 7. 21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: a multicenter study.
    Moran C, Azziz R, Carmina E, Dewailly D, Fruzzetti F, Ibañez L, Knochenhauer ES, Marcondes JA, Mendonca BB, Pignatelli D, Pugeat M, Rohmer V, Speiser PW, Witchel SF.
    Am J Obstet Gynecol; 2000 Dec 15; 183(6):1468-74. PubMed ID: 11120512
    [Abstract] [Full Text] [Related]

  • 8. Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency.
    Dewailly D, Vantyghem-Haudiquet MC, Sainsard C, Buvat J, Cappoen JP, Ardaens K, Racadot A, Lefebvre J, Fossati P.
    J Clin Endocrinol Metab; 1986 Aug 15; 63(2):418-23. PubMed ID: 3013919
    [Abstract] [Full Text] [Related]

  • 9. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Khandekar S, Lata V, Dash RJ.
    Indian J Med Res; 1990 Apr 15; 92():79-82. PubMed ID: 2164496
    [Abstract] [Full Text] [Related]

  • 10. [Hirsutism in Chilean women: importance of 21-hydroxylase congenital deficiency of late onset].
    Gallardo E, Porcile A.
    Rev Med Chil; 1991 Feb 15; 119(2):147-51. PubMed ID: 1824156
    [Abstract] [Full Text] [Related]

  • 11. Screening for late-onset congenital adrenal hyperplasia in hirsutism or amenorrhea.
    Baskin HJ.
    Arch Intern Med; 1987 May 15; 147(5):847-8. PubMed ID: 3579438
    [Abstract] [Full Text] [Related]

  • 12. 21-Hydroxylase deficiency in female hyperandrogenism: screening and diagnosis.
    Azziz R, Zacur HA.
    J Clin Endocrinol Metab; 1989 Sep 15; 69(3):577-84. PubMed ID: 2547827
    [Abstract] [Full Text] [Related]

  • 13. Adrenal androgen excess and defective 11 beta-hydroxylation in women with idiopathic hirsutism.
    Guthrie GP, Wilson EA, Quillen DL, Jawad MJ.
    Arch Intern Med; 1982 Apr 15; 142(4):729-35. PubMed ID: 6978695
    [Abstract] [Full Text] [Related]

  • 14. Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia.
    Eldar-Geva T, Hurwitz A, Vecsei P, Palti Z, Milwidsky A, Rösler A.
    N Engl J Med; 1990 Sep 27; 323(13):855-63. PubMed ID: 2168516
    [Abstract] [Full Text] [Related]

  • 15. [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 Sep 27; 49(5):295-9. PubMed ID: 6242254
    [No Abstract] [Full Text] [Related]

  • 16. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.
    J Clin Endocrinol Metab; 1982 Nov 27; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

  • 17. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
    Chrousos GP, Loriaux DL, Mann D, Cutler GB.
    Horm Res; 1982 Nov 27; 16(4):193-200. PubMed ID: 6290362
    [Abstract] [Full Text] [Related]

  • 18. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
    Kohn B, Levine LS, Pollack MS, Pang S, Lorenzen F, Levy D, Lerner AJ, Rondanini GF, Dupont B, New MI.
    J Clin Endocrinol Metab; 1982 Nov 27; 55(5):817-27. PubMed ID: 6288753
    [Abstract] [Full Text] [Related]

  • 19. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A, Stivel M, Zamir R, Kaufman H, Pertzelan A, Laron Z.
    Isr J Med Sci; 1982 Jul 27; 18(7):763-8. PubMed ID: 6980865
    [Abstract] [Full Text] [Related]

  • 20. The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).
    Carmina E, Gagliano AM, Rosato F, Maggiore M, Jannì A.
    J Endocrinol Invest; 1984 Apr 27; 7(2):89-92. PubMed ID: 6327799
    [Abstract] [Full Text] [Related]

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