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Journal Abstract Search

408 related items for PubMed ID: 8469492

  • 21. P450scc deficiency (congenital lipoid adrenal hyperplasia): first reported case in Thailand and literature review.
    Jaruratanasirikul S.
    J Med Assoc Thai; 1996 Aug; 79(8):531-5. PubMed ID: 8855637
    [Abstract] [Full Text] [Related]

  • 22. Familial lipoid adrenal hyperplasia: genetic marker data and an approach to prenatal diagnosis.
    Frydman M, Kauschansky A, Zamir R, Bonné-Tamir B.
    Am J Med Genet; 1986 Oct; 25(2):319-25. PubMed ID: 3465240
    [Abstract] [Full Text] [Related]

  • 23. [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 Oct; 108(11-12):497-500. PubMed ID: 3573974
    [No Abstract] [Full Text] [Related]

  • 24. Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia.
    Pang S, Clark AT, Freeman LC, Dolan LM, Immken L, Mueller OT, Stiff D, Shulman DI.
    J Clin Endocrinol Metab; 1992 Jul; 75(1):249-53. PubMed ID: 1619017
    [Abstract] [Full Text] [Related]

  • 25. [Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies].
    Nivelon JL, Chouchane M, Forest MG, Morel Y, Huet F, Nivelon-Chevallier A, François C.
    Ann Pediatr (Paris); 1993 Sep; 40(7):421-5. PubMed ID: 7902059
    [Abstract] [Full Text] [Related]

  • 26. [Pregnanetriol in the amniotic fluid: prenatal diagnosis of adrenogenital syndrome by amniocentesis (author's transl)].
    Holzmann K, Wittenbecher G, Mickan H.
    Geburtshilfe Frauenheilkd; 1974 May; 34(5):364-8. PubMed ID: 4849448
    [No Abstract] [Full Text] [Related]

  • 27. 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 May; 458():130-47. PubMed ID: 3879118
    [No Abstract] [Full Text] [Related]

  • 28. [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]

  • 29. [Prenatal diagnosis and treatment of congenital adrenal gland hyperplasia].
    Igea García JM, Martul Tobio P, Loridan Stienlet L, Pineda Algorta J.
    An Esp Pediatr; 1992 Jun 05; 36 Suppl 49():138-40. PubMed ID: 1416452
    [No Abstract] [Full Text] [Related]

  • 30. [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 15; 130(7):206-9. PubMed ID: 1826462
    [Abstract] [Full Text] [Related]

  • 31. [Prenatal diagnosis of adrenogenital syndrome].
    Teller WM.
    Dtsch Med Wochenschr; 1972 Jan 21; 97(3):89-90. PubMed ID: 5007399
    [No Abstract] [Full Text] [Related]

  • 32. [Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency].
    Dumić M, Ille J, Brkljacić L, Plavsić V, Drazancić A, Banicević M, Radmanović S, Filipović B, Suchanek E, Kastelan A.
    Lijec Vjesn; 1989 Jan 21; 111(9-10):312-7. PubMed ID: 2633007
    [Abstract] [Full Text] [Related]

  • 33. [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 21; 86(5-6):189-94. PubMed ID: 7349743
    [No Abstract] [Full Text] [Related]

  • 34. 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 Jan 21; 458():111-29. PubMed ID: 3879117
    [No Abstract] [Full Text] [Related]

  • 35. Congenital lipoid hyperplasia of the fetal adrenal gland.
    Moragas A, Ballabriga A.
    Helv Paediatr Acta; 1969 Apr 21; 24(2):226-38. PubMed ID: 5816620
    [No Abstract] [Full Text] [Related]

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

  • 37. A family at risk of congenital adrenal hyperplasia: a molecular approach for prenatal diagnosis.
    Ruangvutilert P, Techatraisak K, Kanokpongsakdi S.
    J Med Assoc Thai; 2001 Dec 21; 84(12):1766-71. PubMed ID: 11999826
    [Abstract] [Full Text] [Related]

  • 38. [Prenatal diagnosis of the congenital adrenogenital syndrome].
    Restagno G, Carbonara AO.
    Minerva Endocrinol; 1987 Dec 21; 12(2):97-100. PubMed ID: 3302652
    [No Abstract] [Full Text] [Related]

  • 39. [Prenatal diagnosis of genetic diseases using chorionic villi].
    Boué J, Deluchat C, Nicolas H, Oury JF, Dumez Y.
    J Genet Hum; 1986 Aug 21; 34(3-4):221-33. PubMed ID: 3760827
    [Abstract] [Full Text] [Related]

  • 40. Prenatal diagnosis and treatment of congenital adrenal hyperplasia and consequences in adults.
    Spiliotis BE.
    J Pediatr Endocrinol Metab; 2001 Aug 21; 14 Suppl 5():1299-302; discussion 1317. PubMed ID: 11964026
    [Abstract] [Full Text] [Related]

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