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Journal Abstract Search

141 related items for PubMed ID: 6965821

  • 1. Adult-onset familial adrenal 21-hydroxylase deficiency.
    Blankstein J, Faiman C, Reyes FI, Schroeder ML, Winter JS.
    Am J Med; 1980 Mar; 68(3):441-8. PubMed ID: 6965821
    [Abstract] [Full Text] [Related]

  • 2. 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; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

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

  • 4. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
    Migeon CJ, Rosenwaks Z, Lee PA, Urban MD, Bias WB.
    J Clin Endocrinol Metab; 1980 Sep; 51(3):647-9. PubMed ID: 6251108
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.
    Chrousos GP, Loriaux DL, Mann DL, Cutler GB.
    Ann Intern Med; 1982 Feb 15; 96(2):143-8. PubMed ID: 6977282
    [Abstract] [Full Text] [Related]

  • 7. Normal gestation and diminished androgen responsiveness in an untreated patient with 21-hydroxylase deficiency.
    Leichter SB, Jacobs LS.
    J Clin Endocrinol Metab; 1976 Mar 15; 42(3):575-82. PubMed ID: 176172
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

  • 9. Recent advances in 21-hydroxylase deficiency.
    New MI, Levine LS.
    Annu Rev Med; 1984 Nov 15; 35():649-63. PubMed ID: 6372675
    [Abstract] [Full Text] [Related]

  • 10. Dexamethasone preparation does not alter corticoid and androgen responses to adrenocorticotropin.
    Rosenfield RL, Helke J, Lucky AW.
    J Clin Endocrinol Metab; 1985 Mar 15; 60(3):585-9. PubMed ID: 2982902
    [Abstract] [Full Text] [Related]

  • 11. [A case of 21-hydroxylase deficiency and Bartter's syndrome associated with a balanced 6-9 translocation].
    Yabe R, Mizuno K, Ojima M, Ogawa S, Hashimoto S, Kunii N, Kishino K, Tani M, Niimura S, Watari H.
    Nihon Naibunpi Gakkai Zasshi; 1986 Aug 20; 62(8):843-56. PubMed ID: 3491009
    [Abstract] [Full Text] [Related]

  • 12. [Hirsutism and light forms of congenital adrenogenital syndrome with 21- and 11-beta hydroxylase defect].
    Zachmann M.
    Schweiz Med Wochenschr; 1986 Mar 29; 116(13):408-12. PubMed ID: 3486468
    [Abstract] [Full Text] [Related]

  • 13. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Mar 29; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1980 Dec 07; 51(6):1316-24. PubMed ID: 6449518
    [Abstract] [Full Text] [Related]

  • 16. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.
    Speiser PW, New MI.
    J Clin Endocrinol Metab; 1987 Jan 07; 64(1):86-91. PubMed ID: 3023431
    [Abstract] [Full Text] [Related]

  • 17. [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 Jan 07; 183(2):117-21. PubMed ID: 2555033
    [Abstract] [Full Text] [Related]

  • 18. Diagnosis and natural history of 17-hydroxylase deficiency in a newborn male.
    Dean HJ, Shackleton CH, Winter JS.
    J Clin Endocrinol Metab; 1984 Sep 07; 59(3):513-20. PubMed ID: 6086702
    [Abstract] [Full Text] [Related]

  • 19. [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 07; 81 Spec No():93-5. PubMed ID: 3142437
    [Abstract] [Full Text] [Related]

  • 20. 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 Jun 07; 16(4):193-200. PubMed ID: 6290362
    [Abstract] [Full Text] [Related]

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