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Journal Abstract Search

154 related items for PubMed ID: 9488957

  • 21. [Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency].
    Dörr HG, Sippell WG, Willig RP.
    Geburtshilfe Frauenheilkd; 1992 Oct; 52(10):586-8. PubMed ID: 1294431
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  • 22. Prenatal dexamethasone treatment of fetuses at risk for congenital adrenal hyperplasia: benefits and concerns.
    Ritzén EM.
    Semin Neonatol; 2001 Aug; 6(4):357-62. PubMed ID: 11972437
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  • 23. [Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency. Position of the Pediatric Endocrinology Study Group of the German Society of Pediatrics and the Section of Pediatric Endocrinology of the German Society of Endocrinology].
    Dörr HG, Sippell WG, Willig RP.
    Monatsschr Kinderheilkd; 1992 Sep; 140(9):661-3. PubMed ID: 1435819
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  • 24. 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 Sep; 6(4):295-300. PubMed ID: 7211946
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  • 28. Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Nimkarn S, New MI.
    Mol Cell Endocrinol; 2009 Mar 05; 300(1-2):192-6. PubMed ID: 19101608
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  • 29. [Prenatal diagnosis of genetic diseases using chorionic villi].
    Boué J, Deluchat C, Nicolas H, Oury JF, Dumez Y.
    J Genet Hum; 1986 Aug 05; 34(3-4):221-33. PubMed ID: 3760827
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  • 32. 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 05; 9(7):457-66. PubMed ID: 2788885
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  • 34. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
    Geifman-Holtzman O, Fay K.
    Am J Med Genet; 1998 Jul 07; 78(3):250-3. PubMed ID: 9677060
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  • 35. 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 07; 84(12):1766-71. PubMed ID: 11999826
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  • 36. [Molecular diagnosis of salt wasting congenital adrenal hyperplasia, caused by deficit of 21-hydroxylase, in the Chilean population].
    Pineda P, Fardella C, Poggi H, Torrealba I, Cattani A, Soto J, Foradori A.
    Rev Med Chil; 1997 Sep 07; 125(9):987-92. PubMed ID: 9595788
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  • 37. Diagnosis and management of congenital adrenal hyperplasia: clinical, molecular and prenatal aspects.
    Mathur R, Kabra M, Menon PS.
    Natl Med J India; 2001 Sep 07; 14(1):26-31. PubMed ID: 11242695
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  • 38. Prenatal diagnosis of congenital lipoid adrenal hyperplasia.
    Izumi H, Saito N, Ichiki S, Makino Y, Yukitake K, Kaneoka T.
    Obstet Gynecol; 1993 May 07; 81(5 ( Pt 2)):839-41. PubMed ID: 8469492
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  • 39. Treating fetal thyroid and adrenal disorders through the mother.
    Van Vliet G, Polak M, Ritzén EM.
    Nat Clin Pract Endocrinol Metab; 2008 Dec 07; 4(12):675-82. PubMed ID: 18981991
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  • 40. 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 07; 38(4):421-5. PubMed ID: 8319374
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