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Journal Abstract Search

196 related items for PubMed ID: 15067252

  • 1. [21 hydroxylase deficiency: new strategies emerging from molecular studies].
    Morel Y, Tardy V, Costa JM, Forest MG, David M.
    Ann Endocrinol (Paris); 2003 Dec; 64(6):456-70. PubMed ID: 15067252
    [No Abstract] [Full Text] [Related]

  • 2. Successful antenatal treatment of an affected congenital adrenal hyperplasia pregnancy using linkage analysis.
    Day DJ, Fitness JE, Milsom S.
    Aust N Z J Obstet Gynaecol; 2004 Aug; 44(4):369-71. PubMed ID: 15282019
    [No Abstract] [Full Text] [Related]

  • 3. [Carrier detection, prenatal diagnosis and treatment in adrenogenital syndrome].
    Illy KE, Oosterwijk JC, Christiaens GC, Wit JM.
    Ned Tijdschr Geneeskd; 1992 Dec 05; 136(49):2411-4. PubMed ID: 1470241
    [No Abstract] [Full Text] [Related]

  • 4. 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 05; 84(9):3129-34. PubMed ID: 10487675
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia using the polymerase chain reaction.
    Owerbach D, Draznin MB, Carpenter RJ, Greenberg F.
    Hum Genet; 1992 Apr 05; 89(1):109-10. PubMed ID: 1349559
    [Abstract] [Full Text] [Related]

  • 6. [Adrenogenital syndrome with 21-hydroxylase deficiency].
    Dörr HG, Sippell WG.
    Monatsschr Kinderheilkd; 1993 Jul 05; 141(7):609-21. PubMed ID: 8413342
    [No Abstract] [Full Text] [Related]

  • 7. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG, Brykova EK, Bakharev VA.
    Akush Ginekol (Mosk); 1990 Jan 05; (1):10-4. PubMed ID: 2353725
    [No Abstract] [Full Text] [Related]

  • 8. Sequential use of hydrocortisone and dexamethasone in prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Uçar A, Saka N, Baş F, Poyrazoğlu S, Bundak R, Darendeliler F.
    Horm Res Paediatr; 2013 Jan 05; 79(5):323-4. PubMed ID: 23711741
    [No Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis and treatment of congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Horm Res; 2007 Jan 05; 67(2):53-60. PubMed ID: 17047340
    [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 05; 18(2):133-42. PubMed ID: 15751602
    [Abstract] [Full Text] [Related]

  • 11. Description and defense of prenatal diagnosis and treatment with low-dose dexamethasone for congenital adrenal hyperplasia.
    New M.
    Am J Bioeth; 2010 Sep 05; 10(9):48-51. PubMed ID: 20818561
    [No Abstract] [Full Text] [Related]

  • 12. How can molecular biology contribute to the management of congenital adrenal hyperplasia?
    Ritzén EM, Lajic S, Wedell A.
    Horm Res; 2000 Sep 05; 53 Suppl 1():34-7. PubMed ID: 10895040
    [Abstract] [Full Text] [Related]

  • 13. [Congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Fujieda K, Mukai T.
    Nihon Rinsho; 2004 Feb 05; 62(2):361-7. PubMed ID: 14968546
    [Abstract] [Full Text] [Related]

  • 14. 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 05; 38(4):421-5. PubMed ID: 8319374
    [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 05; 165(Pt A):121-123. PubMed ID: 27378492
    [Abstract] [Full Text] [Related]

  • 16. [Abnormal production of adrenal gland hormones--special reference to congenital adrenal hyperplasia].
    Igarashi Y.
    Nihon Naibunpi Gakkai Zasshi; 1991 Jun 20; 67 Suppl 3():740-5. PubMed ID: 1915976
    [No Abstract] [Full Text] [Related]

  • 17. Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia.
    Wedell A.
    Clin Lab Med; 1996 Mar 20; 16(1):125-37. PubMed ID: 8867587
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Passarge E.
    Indian J Pediatr; 1988 Mar 20; 55(4):472-5. PubMed ID: 3262582
    [No Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis and treatment of congenital adrenal hyperplasia.
    Speiser PW, New MI.
    J Pediatr Endocrinol; 1994 Mar 20; 7(3):183-91. PubMed ID: 7820211
    [Abstract] [Full Text] [Related]

  • 20. Mutations in steroid 21-hydroxylase (CYP21).
    White PC, Tusie-Luna MT, New MI, Speiser PW.
    Hum Mutat; 1994 Mar 20; 3(4):373-8. PubMed ID: 8081391
    [Abstract] [Full Text] [Related]

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