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Journal Abstract Search

101 related items for PubMed ID: 316370

  • 1. Adrenal steroidogenesis in heterozygotes for 21-hydroxylase deficiency.
    Child DF, Bu'lock DE, Anderson DC.
    Clin Endocrinol (Oxf); 1979 Oct; 11(4):391-8. PubMed ID: 316370
    [No Abstract] [Full Text] [Related]

  • 2. Diagnosis of homozygosity and heterozygosity in congenital adrenal hyperplasia (CAH) and control of treatment.
    Knorr D, Bidlingmaier F, Höller W, Kuhnle U.
    J Steroid Biochem; 1983 Jul; 19(1B):645-53. PubMed ID: 6887889
    [Abstract] [Full Text] [Related]

  • 3. Defective 11 beta hydroxylation in patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency.
    Kolanowski J, Crabbe J.
    Ann Endocrinol (Paris); 1981 Dec; 42(6):537-8. PubMed ID: 6980618
    [No Abstract] [Full Text] [Related]

  • 4. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Winkel CA, Casey ML, Worley RJ, Madden JD, MacDonald PC.
    J Clin Endocrinol Metab; 1983 Jan; 56(1):104-7. PubMed ID: 6600168
    [Abstract] [Full Text] [Related]

  • 5. HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population.
    Couillin P, Rappaport R, Kuttenn F, Canlorbe P, Hors J, Marcelli-Barge A, Feingold J, Grisard MC, Boué J, Boué A.
    Tissue Antigens; 1982 Feb; 19(2):100-7. PubMed ID: 6980498
    [No Abstract] [Full Text] [Related]

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

  • 7. Disorders of adrenal steroidogenesis.
    Drucker S, New MI.
    Pediatr Clin North Am; 1987 Aug; 34(4):1055-66. PubMed ID: 3302892
    [Abstract] [Full Text] [Related]

  • 8. [Hormonal profile and HLA typing of adult subjects from 7 families with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Bercovici JP, Tater D, Khoury S, Le Fur JM, Saleun JP, Nahoul K, Scholler R.
    Ann Endocrinol (Paris); 1982 Aug; 43(3):203-11. PubMed ID: 6984316
    [Abstract] [Full Text] [Related]

  • 9. Nonclassic adrenal hyperplasia due to 21-hydroxylase deficiency.
    Drucker S, New MI.
    Pediatr Clin North Am; 1987 Aug; 34(4):1067-81. PubMed ID: 3302893
    [Abstract] [Full Text] [Related]

  • 10. Circadian variation of plasma 17-hydroxyprogesterone among heterozygotic carriers of 21-hydroxylase deficiency (salt-losing form).
    Urban MD, Migeon CJ, Lee PA.
    Horm Res; 1986 Aug; 23(2):74-7. PubMed ID: 3484712
    [Abstract] [Full Text] [Related]

  • 11. Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Gutai JP, Lee PA, Johnsonbaugh RE, Gareis F, Urban MD, Migeon CJ.
    J Pediatr; 1979 May; 94(5):770-2. PubMed ID: 221633
    [No Abstract] [Full Text] [Related]

  • 12. Steroid excretion in urine during suppression and stimulation of adrenals in the 17 alpha-hydroxylase deficiency syndrome.
    Honour J, Millar G, Roitman E, Shackleton C.
    J Clin Endocrinol Metab; 1981 May; 52(5):1039-42. PubMed ID: 6262355
    [Abstract] [Full Text] [Related]

  • 13. Prenatal treatment in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: up-date 88 of the French multicentric study.
    Forest MG, Bétuel H, David M.
    Endocr Res; 1989 May; 15(1-2):277-301. PubMed ID: 2667968
    [Abstract] [Full Text] [Related]

  • 14. "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.
    New MI, Lorenzen F, Pang S, Gunczler P, Dupont B, Levine LS.
    J Clin Endocrinol Metab; 1979 Feb; 48(2):356-9. PubMed ID: 218988
    [Abstract] [Full Text] [Related]

  • 15. [Modern methods in the diagnosis of hyperandrogenic dysfunction due to adrenal 21-hydroxylase deficiency].
    Campagnoli C, Battistini M, Dolfin AM, Lanza MG, Peris C, Santoro C, Siliquini GP.
    Minerva Ginecol; 1981 Jun; 33(6):563-5. PubMed ID: 7279278
    [No Abstract] [Full Text] [Related]

  • 16. Heterozygotes for 17 alpha-hydroxylase deficiency can be detected with a short ACTH test.
    Wit JM, van Roermund HP, Oostdijk W, Benraad TJ, Thijssen JH, Boer P, Jansen M, Spit M, van den Brande JL.
    Clin Endocrinol (Oxf); 1988 Jun; 28(6):657-64. PubMed ID: 2855412
    [Abstract] [Full Text] [Related]

  • 17. Adrenogenital syndrome due to 11-beta-hydroxylase deficiency with skeletal abnormalities and pulmonary stenosis.
    Ajlouni K, El-Zaheri M, Habbab M, Qoussous Y, El-Khateeb M.
    J Endocrinol Invest; 1984 Apr; 7(2):129-31. PubMed ID: 6609951
    [Abstract] [Full Text] [Related]

  • 18. MHC "supratype" predicting heterozygous 21-hydroxylase deficiency.
    McCluskey J, Kay PH, Stuckey M, Christiansen FT, Dawkins RL, Wilson G.
    Lancet; 1983 Apr 02; 1(8327):764-5. PubMed ID: 6132105
    [No Abstract] [Full Text] [Related]

  • 19. HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.
    Couillin P, Rappaport R, Kuttenn F, Hors J, Feingold J, Boué J, Boué A.
    Ann N Y Acad Sci; 1985 Apr 02; 458():41-5. PubMed ID: 3879129
    [No Abstract] [Full Text] [Related]

  • 20. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.
    Bacon GE, Kelch RP.
    J Endocrinol Invest; 1979 Apr 02; 2(1):93-100. PubMed ID: 385704
    [No Abstract] [Full Text] [Related]

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