BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 7349743)

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

  • 2. [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]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. [Levels of 17 alpha-hydroxyprogesterone and cortisol in the amniotic fluid in pregnancy with normal fetus and in fetal diseases].
    Dzenis IG; Brykova EK; Bakharev VA; Fanchenko ND
    Akush Ginekol (Mosk); 1989 Jan; (1):63-5. PubMed ID: 2712226
    [No Abstract]   [Full Text] [Related]  

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

  • 7. 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; 66(3):534-7. PubMed ID: 3258316
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Determination of steroid hormones in the amniotic fluid in prenatal genetic diagnosis].
    Dvorák P; Macek M; Hampl R; Sulcová J; Burjanková J; Stárka L
    Cas Lek Cesk; 1991 Feb; 130(7):206-9. PubMed ID: 1826462
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interferences with determination of 17-hydroxyprogesterone in amniotic fluid.
    Plavsić V; Rogić D; Dumić M; Ille J; Brkljacić L; Latin V
    Clin Chem; 1991 Dec; 37(12):2154-5. PubMed ID: 1764804
    [No Abstract]   [Full Text] [Related]  

  • 11. Amniotic fluid steroid levels and fetal adrenal weight in congenital adrenal hyperplasia.
    Hughes IA; Dyas J; Laurence KM
    Horm Res; 1987; 28(1):20-4. PubMed ID: 3502335
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [17-Hydroxyprogesterone levels in the amniotic fluid during the 2d trimester of pregnancy].
    Bakharev VA; Dzenis IG; Kolesnikova GS; Polesterov IuA
    Probl Endokrinol (Mosk); 1987; 33(3):20-2. PubMed ID: 2443910
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 9(7):457-66. PubMed ID: 2788885
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Progress in the prenatal diagnosis of adrenogenital syndrome].
    Blaim A
    Ginekol Pol; 1984 Feb; 55(2):137-41. PubMed ID: 6381241
    [No Abstract]   [Full Text] [Related]  

  • 15. 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; 322(2):111-5. PubMed ID: 2403652
    [No Abstract]   [Full Text] [Related]  

  • 16. Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk.
    Forest MG
    Ann N Y Acad Sci; 1985; 458():130-47. PubMed ID: 3879118
    [No Abstract]   [Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. 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; 458():111-29. PubMed ID: 3879117
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 9.