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Journal Abstract Search

162 related items for PubMed ID: 517576

  • 1. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979; 4(2):201-4. PubMed ID: 517576
    [Abstract] [Full Text] [Related]

  • 2. Amniotic 17-alpha hydroxyprogesterone and HLA typing for the prenatal diagnosis of 21-alpha hydroxylase deficiency--congenital adrenal hyperplasia.
    Rosenmann A, Schumert Z, Theodor R, Cohen T, Brautbar C.
    Am J Med Genet; 1980; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 3. [Prenatal diagnosis of congenital adrenal hyperplasia due to a 21-hydroxylase defect--determination of 17-hydroxyprogesterone in the amniotic fluid].
    Dumić M, Plavsić V, Ille J, Brkljacić L, Drazanćić A, Suchanek E, Kaśtelan A.
    Lijec Vjesn; 1987; 109(2-3):65-7. PubMed ID: 3496509
    [No Abstract] [Full Text] [Related]

  • 4. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.
    J Clin Endocrinol Metab; 1985 Jul; 61(1):89-97. PubMed ID: 3873469
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of congenital adrenal hyperplasia.
    Warsof SL, Larsen JW, Kent SG, Rosenbaum KN, August GP, Migeon CJ, Schulman JD.
    Obstet Gynecol; 1980 Jun; 55(6):751-4. PubMed ID: 7383464
    [Abstract] [Full Text] [Related]

  • 6. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Couillin P.
    Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534
    [Abstract] [Full Text] [Related]

  • 7. [Congenital adrenal hyperplasia and HLA antigens].
    Boué A, Boué J, Couillin P.
    J Genet Hum; 1980 Sep 21; 28(3):195-200. PubMed ID: 7463017
    [No Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.
    Gueux B, Fiet J, Couillin P, Raux-Demay MC, Mornet E, Galons H, Villette JM, Boue J, Dreux C.
    J Clin Endocrinol Metab; 1988 Mar 21; 66(3):534-7. PubMed ID: 3258316
    [Abstract] [Full Text] [Related]

  • 9. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].
    Lambotte C.
    Rev Med Liege; 1986 Jan 15; 41(2):37-44. PubMed ID: 3006204
    [No Abstract] [Full Text] [Related]

  • 10. [Determination of 17-hydroxyprogesterone in the amniotic fluid: clinical significance].
    Catalano D, Valentino R, Troncone MG, Daniele F, Rullo F.
    Arch Ostet Ginecol; 1981 Jan 15; 86(5-6):189-94. PubMed ID: 7349743
    [No Abstract] [Full Text] [Related]

  • 11. Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.
    Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A.
    Prenat Diagn; 1989 Jul 15; 9(7):457-66. PubMed ID: 2788885
    [Abstract] [Full Text] [Related]

  • 12. [Prenatal detection of congenital adrenal hyperplasia using HLA typing of fetal cells from the amniotic fluid].
    Brkljacić L, Dumić M, Plavsić V, Drazancić A, Gerencer M, Kastelan A.
    Lijec Vjesn; 1986 Jul 15; 108(11-12):497-500. PubMed ID: 3573974
    [No Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAH.
    Forest MG, Bétuel H, Couillin P, Boué A.
    Prenat Diagn; 1981 Jul 15; 1(3):197-207. PubMed ID: 6981108
    [Abstract] [Full Text] [Related]

  • 14. HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAH.
    Grosse-Wilde H, Valentine-Thon E, Vögeler U, Passarge E, Lorenzen F, Sippell WG, Bidlingmaier F, Knorr D.
    Prenat Diagn; 1988 Feb 15; 8(2):131-43. PubMed ID: 3258985
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of congenital adrenal hyperplasia.
    Levine LS, New MI, Pollack M, Dupont B.
    Lancet; 1979 Sep 22; 2(8143):637. PubMed ID: 90299
    [No Abstract] [Full Text] [Related]

  • 16. [Prenatal diagnosis of congenital hyperplasia of the adrenal cortex].
    Dzenis IG, Brykova EK, Bronshteĭn MI, Bakharev VA, Fanchenko ND.
    Sov Med; 1988 Sep 22; (7):11-4. PubMed ID: 3227442
    [No Abstract] [Full Text] [Related]

  • 17. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.
    Ann N Y Acad Sci; 1985 Sep 22; 458():111-29. PubMed ID: 3879117
    [No Abstract] [Full Text] [Related]

  • 18. [21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive].
    Simonin G, Palix C, Roulier R, Coignet J.
    Ann Pediatr (Paris); 1986 May 22; 33(5):423-7. PubMed ID: 3729253
    [No Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by amniotic fluid steroid analysis.
    Hughes IA, Laurence KM.
    Prenat Diagn; 1982 Apr 22; 2(2):97-102. PubMed ID: 6983064
    [Abstract] [Full Text] [Related]

  • 20. 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]

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