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Journal Abstract Search

178 related items for PubMed ID: 10895040

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

  • 2. [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]

  • 3. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Forest MG.
    Hum Reprod Update; 2004 Dec; 10(6):469-85. PubMed ID: 15514016
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, Lin-Su K, New MI.
    Endocrinol Metab Clin North Am; 2009 Dec; 38(4):699-718. PubMed ID: 19944288
    [Abstract] [Full Text] [Related]

  • 6. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Coeli-Lacchini FB, Turatti W, Elias PC, Elias LL, Martinelli CE, Moreira AC, Antonini SR, de Castro M.
    Gene; 2013 Sep 10; 526(2):239-45. PubMed ID: 23570880
    [Abstract] [Full Text] [Related]

  • 7. Prenatal treatment of congenital adrenal hyperplasia. The United States experience.
    New MI.
    Endocrinol Metab Clin North Am; 2001 Mar 10; 30(1):1-13. PubMed ID: 11344929
    [Abstract] [Full Text] [Related]

  • 8. Mutations in steroid 21-hydroxylase (CYP21).
    White PC, Tusie-Luna MT, New MI, Speiser PW.
    Hum Mutat; 1994 Mar 10; 3(4):373-8. PubMed ID: 8081391
    [Abstract] [Full Text] [Related]

  • 9.
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    [No Abstract] [Full Text] [Related]

  • 10. Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.
    Lekarev O, Tafuri K, Lane AH, Zhu G, Nakamoto JM, Buller-Burckle AM, Wilson TA, New MI.
    J Perinatol; 2013 Jan 10; 33(1):76-8. PubMed ID: 23269230
    [Abstract] [Full Text] [Related]

  • 11. 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 10; 89(1):109-10. PubMed ID: 1349559
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis and treatment of congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Horm Res; 2007 Apr 10; 67(2):53-60. PubMed ID: 17047340
    [Abstract] [Full Text] [Related]

  • 13. [Congenital adrenal hyperplasia].
    Bouvattier C, Chatelain P.
    Rev Prat; 2008 May 15; 58(9):990-4. PubMed ID: 18672665
    [Abstract] [Full Text] [Related]

  • 14. Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia.
    Wedell A.
    Clin Lab Med; 1996 Mar 15; 16(1):125-37. PubMed ID: 8867587
    [Abstract] [Full Text] [Related]

  • 15. An update on the molecular genetics of congenital adrenal hyperplasia: diagnostic and therapeutic aspects.
    Wedell A.
    J Pediatr Endocrinol Metab; 1998 Mar 15; 11(5):581-9. PubMed ID: 9829208
    [Abstract] [Full Text] [Related]

  • 16. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    White PC, Speiser PW.
    Endocr Rev; 2000 Jun 15; 21(3):245-91. PubMed ID: 10857554
    [Abstract] [Full Text] [Related]

  • 17. [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 15; (1):10-4. PubMed ID: 2353725
    [No Abstract] [Full Text] [Related]

  • 18. Diagnosis and management of classical congenital adrenal hyperplasia.
    Marumudi E, Khadgawat R, Surana V, Shabir I, Joseph A, Ammini AC.
    Steroids; 2013 Aug 15; 78(8):741-6. PubMed ID: 23624029
    [Abstract] [Full Text] [Related]

  • 19. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A paradigm for prenatal diagnosis and treatment.
    Nimkarn S, New MI.
    Ann N Y Acad Sci; 2010 Mar 15; 1192():5-11. PubMed ID: 20392211
    [Abstract] [Full Text] [Related]

  • 20. Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.
    Dolzan V, Sólyom J, Fekete G, Kovács J, Rakosnikova V, Votava F, Lebl J, Pribilincova Z, Baumgartner-Parzer SM, Riedl S, Waldhauser F, Frisch H, Stopar-Obreza M, Krzisnik C, Battelino T.
    Eur J Endocrinol; 2005 Jul 15; 153(1):99-106. PubMed ID: 15994751
    [Abstract] [Full Text] [Related]

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