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Journal Abstract Search

141 related items for PubMed ID: 3267357

  • 1. Prenatal diagnosis of a heterozygote of salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency by genetic linkage analysis.
    Oh BH, Park JK, Choi YM, Yang IM, Kim YS, Choi YK.
    J Korean Med Sci; 1988 Jun; 3(2):73-7. PubMed ID: 3267357
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  • 4. 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; 8(2):131-43. PubMed ID: 3258985
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  • 5. 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
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  • 6. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in Croatia.
    Dumic M, Brkljacic L, Plavsic V, Zunec R, Ille J, Wilson RC, Kuvacic I, Kastelan A, New MI.
    Am J Med Genet; 1997 Oct 31; 72(3):302-6. PubMed ID: 9332659
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  • 7. 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 Oct 31; 6(4):295-300. PubMed ID: 7211946
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  • 8. Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia.
    Fiet J, Gueux B, Gourmelen M, Kuttenn F, Vexiau P, Couillin P, Pham-Huu-Trung MT, Villette JM, Raux-Demay MC, Galons H.
    J Clin Endocrinol Metab; 1988 Apr 31; 66(4):659-67. PubMed ID: 2831244
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  • 9. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.
    J Clin Endocrinol Metab; 1982 Nov 31; 55(5):866-71. PubMed ID: 6288754
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  • 10. 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 31; 1(3):197-207. PubMed ID: 6981108
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  • 11. Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: effect on midgestational amniotic fluid steroid levels.
    Dörr HG, Sippell WG.
    J Clin Endocrinol Metab; 1993 Jan 31; 76(1):117-20. PubMed ID: 8421074
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  • 12. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Jan 31; 43(1):3-14. PubMed ID: 6982657
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  • 13. 'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population.
    Dumić M, Brkljacić L, Mardesić D, Plavsić V, Lukenda M, Kastelan A.
    Acta Endocrinol (Copenh); 1985 Jul 31; 109(3):386-92. PubMed ID: 2992207
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  • 14. [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
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  • 15. Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway.
    Fiet J, Gueux B, Raux-DeMay MC, Kuttenn F, Vexiau P, Brerault JL, Couillin P, Galons H, Villette JM, Julien R.
    J Clin Endocrinol Metab; 1989 Mar 21; 68(3):542-7. PubMed ID: 2537337
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  • 16. Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal life.
    Kuhnle U, Böhm N, Wolff G, Mayerová A, Dörr HG, Bidlingmaier F, Knorr D.
    J Clin Endocrinol Metab; 1984 Mar 21; 58(3):574-7. PubMed ID: 6607266
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  • 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 21; 55(6):751-4. PubMed ID: 7383464
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  • 18. Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studies.
    Petersen KE, Svejgaard A, Nielsen MD, Dissing J.
    Horm Res; 1982 Jun 21; 16(3):151-9. PubMed ID: 6286442
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  • 20. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Levine LS, Lorenzen F, Chow D, Pollack M, Dupont B, Genel M, New MI.
    J Clin Endocrinol Metab; 1980 Mar 21; 50(3):586-9. PubMed ID: 6244328
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