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133 related items for PubMed ID: 7829612

  • 1. Prenatal diagnosis of congenital lipoid adrenal hyperplasia.
    Saenger P, Klonari Z, Black SM, Compagnone N, Mellon SH, Fleischer A, Abrams CA, Shackelton CH, Miller WL.
    J Clin Endocrinol Metab; 1995 Jan; 80(1):200-5. PubMed ID: 7829612
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of congenital lipoid adrenal hyperplasia.
    Izumi H, Saito N, Ichiki S, Makino Y, Yukitake K, Kaneoka T.
    Obstet Gynecol; 1993 May; 81(5 ( Pt 2)):839-41. PubMed ID: 8469492
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Heterozygous mutation in the cholesterol side chain cleavage enzyme (p450scc) gene in a patient with 46,XY sex reversal and adrenal insufficiency.
    Tajima T, Fujieda K, Kouda N, Nakae J, Miller WL.
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3820-5. PubMed ID: 11502818
    [Abstract] [Full Text] [Related]

  • 5. 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; 76(1):117-20. PubMed ID: 8421074
    [Abstract] [Full Text] [Related]

  • 6. Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasia.
    Lin D, Gitelman SE, Saenger P, Miller WL.
    J Clin Invest; 1991 Dec; 88(6):1955-62. PubMed ID: 1661294
    [Abstract] [Full Text] [Related]

  • 7. Congenital lipoid adrenal hyperplasia--genes for P450scc, side chain cleavage enzyme, are normal.
    Saenger P, Lin D, Gitelman SE, Miller WL.
    J Steroid Biochem Mol Biol; 1993 Apr; 45(1-3):87-97. PubMed ID: 8481356
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of congenital lipoid adrenal hyperplasia (CLAH) by estriol amniotic fluid analysis and molecular genetic testing.
    Jean A, Mansukhani M, Oberfield SE, Fennoy I, Nakamoto J, Atwan M, Lerer I, Neriah ZB, Zangen DH, Chung WK.
    Prenat Diagn; 2008 Jan; 28(1):11-4. PubMed ID: 18058976
    [Abstract] [Full Text] [Related]

  • 9. 11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
    Rösler A, Weshler N, Leiberman E, Hochberg Z, Weidenfeld J, Sack J, Chemke J.
    J Clin Endocrinol Metab; 1988 Apr; 66(4):830-8. PubMed ID: 3346360
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism.
    Siegel SF, Finegold DN, Lanes R, Lee PA.
    N Engl J Med; 1990 Sep 27; 323(13):849-54. PubMed ID: 2168515
    [Abstract] [Full Text] [Related]

  • 12. 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 27; 3(2):73-7. PubMed ID: 3267357
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of congenital adrenal hyperplasia.
    Warsof SL, Larsen JW, Kent SG, Rosenbaum KN, August GP, Migeon CJ, Schulman JD.
    Obstet Gynecol; 1980 Jun 27; 55(6):751-4. PubMed ID: 7383464
    [Abstract] [Full Text] [Related]

  • 14. [Molecular genetic analysis of congenital lipoid adrenal hyperplasia].
    Qiu WJ, Ye J, Han B, Han LS, Gu XF.
    Zhonghua Er Ke Za Zhi; 2004 Aug 27; 42(8):585-8. PubMed ID: 15347444
    [Abstract] [Full Text] [Related]

  • 15. Profiling steroid hormones in amniotic fluid of midpregnancy by routine stable isotope dilution/gas chromatography-mass spectrometry: reference values and concentrations in fetuses at risk for 21-hydroxylase deficiency.
    Wudy SA, Dörr HG, Solleder C, Djalali M, Homoki J.
    J Clin Endocrinol Metab; 1999 Aug 27; 84(8):2724-8. PubMed ID: 10443667
    [Abstract] [Full Text] [Related]

  • 16. 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 Aug 27; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 17. Amniotic fluid steroid levels and fetal adrenal weight in congenital adrenal hyperplasia.
    Hughes IA, Dyas J, Laurence KM.
    Horm Res; 1987 Aug 27; 28(1):20-4. PubMed ID: 3502335
    [Abstract] [Full Text] [Related]

  • 18. A genetic isolate of congenital lipoid adrenal hyperplasia with atypical clinical findings.
    Chen X, Baker BY, Abduljabbar MA, Miller WL.
    J Clin Endocrinol Metab; 2005 Feb 27; 90(2):835-40. PubMed ID: 15546900
    [Abstract] [Full Text] [Related]

  • 19. Amniotic fluid steroid levels. Fetuses with adrenal hyperplasia, 46,XXY fetuses, and normal fetuses.
    Carson DJ, Okuno A, Lee PA, Stetten G, Didolkar SM, Migeon CJ.
    Am J Dis Child; 1982 Mar 27; 136(3):218-22. PubMed ID: 7064946
    [Abstract] [Full Text] [Related]

  • 20. Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.
    Ma D, Ge H, Li X, Jiang T, Chen F, Zhang Y, Hu P, Chen S, Zhang J, Ji X, Xu X, Jiang H, Chen M, Wang W, Xu Z.
    Gene; 2014 Jul 10; 544(2):252-8. PubMed ID: 24768736
    [Abstract] [Full Text] [Related]

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