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Journal Abstract Search

160 related items for PubMed ID: 2746796

  • 1. Prenatal fetal adrenal suppression following in utero diagnosis of congenital adrenal hyperplasia.
    Shapiro E, Santiago JV, Crane JP.
    J Urol; 1989 Aug; 142(2 Pt 2):663-6; discussion 667-8. PubMed ID: 2746796
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia.
    Cerame BI, Newfield RS, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC.
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3129-34. PubMed ID: 10487675
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency.
    Haan EA, Serjeantson SW, Norman R, Rollond AK, Antonis P, Richards RI, Penfold JL.
    Med J Aust; 1992 Jan 20; 156(2):132-5. PubMed ID: 1736054
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in Croatia.
    Dumic M, Brkljacic L, Plavsic V, Zunec R, Ille J, Wilson RC, Kuvacic I, Kastelan A, New MI.
    Am J Med Genet; 1997 Oct 31; 72(3):302-6. PubMed ID: 9332659
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis and treatment of congenital adrenal hyperplasia.
    Levine LS, Pang S.
    J Pediatr Endocrinol; 1994 Oct 31; 7(3):193-200. PubMed ID: 7820212
    [Abstract] [Full Text] [Related]

  • 6. Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment.
    Carlson AD, Obeid JS, Kanellopoulou N, Wilson RC, New MI.
    J Steroid Biochem Mol Biol; 1999 Oct 31; 69(1-6):19-29. PubMed ID: 10418977
    [Abstract] [Full Text] [Related]

  • 7. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E.
    J Clin Endocrinol Metab; 1990 Apr 31; 70(4):838-48. PubMed ID: 1969421
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis and treatment of adrenogenital syndrome (steroid 21-hydroxylase deficiency).
    New MI.
    Dev Pharmacol Ther; 1990 Apr 31; 15(3-4):200-10. PubMed ID: 2099900
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia).
    Karaviti LP, Mercado AB, Mercado MB, Speiser PW, Buegeleisen M, Crawford C, Antonian L, White PC, New MI.
    J Steroid Biochem Mol Biol; 1992 Mar 31; 41(3-8):445-51. PubMed ID: 1562517
    [Abstract] [Full Text] [Related]

  • 10. Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
    Motaghedi R, Betensky BP, Slowinska B, Cerame B, Cabrer M, New MI, Wilson RC.
    J Pediatr Endocrinol Metab; 2005 Feb 31; 18(2):133-42. PubMed ID: 15751602
    [Abstract] [Full Text] [Related]

  • 11. Prenatal treatment of congenital adrenal hyperplasia: report of a new case.
    Loeuille GA, David M, Forest MG.
    Eur J Pediatr; 1990 Jan 31; 149(4):237-40. PubMed ID: 2406146
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies.
    New MI, Carlson A, Obeid J, Marshall I, Cabrera MS, Goseco A, Lin-Su K, Putnam AS, Wei JQ, Wilson RC.
    J Clin Endocrinol Metab; 2001 Dec 31; 86(12):5651-7. PubMed ID: 11739415
    [Abstract] [Full Text] [Related]

  • 13. Pharmacologic suppression of the fetal adrenal gland in utero. Attempted prevention of abnormal external genital masculinization in suspected congenital adrenal hyperplasia.
    Evans MI, Chrousos GP, Mann DW, Larsen JW, Green I, McCluskey J, Loriaux DL, Fletcher JC, Koons G, Overpeck J.
    JAMA; 1985 Feb 15; 253(7):1015-20. PubMed ID: 3968825
    [Abstract] [Full Text] [Related]

  • 14. The effect on the fetal pituitary-adrenal axis of dexamethasone administration early in the second trimester of pregnancy.
    Mesogitis S, Daskalakis G, Papapetrou P, Mavroudis K, Papandroulaki F, Papantoniou N, Antsaklis A.
    J Matern Fetal Neonatal Med; 2011 Jan 15; 24(1):109-12. PubMed ID: 20528220
    [Abstract] [Full Text] [Related]

  • 15. New developments in prenatal diagnosis of congenital adrenal hyperplasia.
    Kazmi D, Bailey J, Yau M, Abu-Amer W, Kumar A, Low M, Yuen T.
    J Steroid Biochem Mol Biol; 2017 Jan 15; 165(Pt A):121-123. PubMed ID: 27378492
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of congenital adrenal hyperplasia by direct detection of mutations in the steroid 21-hydroxylase gene.
    Rumsby G, Honour JW, Rodeck C.
    Clin Endocrinol (Oxf); 1993 Apr 15; 38(4):421-5. PubMed ID: 8319374
    [Abstract] [Full Text] [Related]

  • 17. Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal life.
    Kuhnle U, Böhm N, Wolff G, Mayerová A, Dörr HG, Bidlingmaier F, Knorr D.
    J Clin Endocrinol Metab; 1984 Mar 15; 58(3):574-7. PubMed ID: 6607266
    [Abstract] [Full Text] [Related]

  • 18. Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang SY, Pollack MS, Marshall RN, Immken L.
    N Engl J Med; 1990 Jan 11; 322(2):111-5. PubMed ID: 2403652
    [No Abstract] [Full Text] [Related]

  • 19. [Prenatal molecular genetic diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Rodríguez A, Ezquieta B, Varela JM, Moreno M, Dulín E, Rodríguez Arnao MD.
    Med Clin (Barc); 1997 Nov 15; 109(17):669-72. PubMed ID: 9488957
    [Abstract] [Full Text] [Related]

  • 20. Challenges in Prenatal Treatment with Dexamethasone.
    McCann-Crosby B, Placencia FX, Adeyemi-Fowode O, Dietrich J, Franciskovich R, Gunn S, Axelrad M, Tu D, Mann D, Karaviti L, Sutton VR.
    Pediatr Endocrinol Rev; 2018 Sep 15; 16(1):186-193. PubMed ID: 30371037
    [Abstract] [Full Text] [Related]

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