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Journal Abstract Search

166 related items for PubMed ID: 3879133

  • 1. Different gene defects in the salt-wasting (SW), simple virilizing (SV), and nonclassical (NC) types of congenital adrenal hyperplasia (CAH).
    Knorr D, Albert ED, Bidlingmaier F, Höller W, Scholz S.
    Ann N Y Acad Sci; 1985; 458():71-5. PubMed ID: 3879133
    [Abstract] [Full Text] [Related]

  • 2. Genetic differences between the salt-wasting, simple virilizing, and nonclassical types of congenital adrenal hyperplasia.
    Höller W, Scholz S, Knorr D, Bidlingmaier F, Keller E, Albert ED.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):757-63. PubMed ID: 2982907
    [Abstract] [Full Text] [Related]

  • 3. [HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population].
    Couillin P, Ravisé N, Hors J, Feingold J, Rappaport R, Kuttenn F, Boué A.
    Pathol Biol (Paris); 1986 Jun; 34(6):789-94. PubMed ID: 3531997
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 Jul; 16(3):151-9. PubMed ID: 6286442
    [Abstract] [Full Text] [Related]

  • 6. Genetics and biochemical variability of variants of 21 hydroxylase deficiency.
    Gordon MT, Conway DI, Anderson DC, Harris R.
    J Med Genet; 1985 Oct; 22(5):354-60. PubMed ID: 3001309
    [Abstract] [Full Text] [Related]

  • 7. 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; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

  • 8. Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.
    Donohoue PA, Van Dop C, Migeon CJ, McLean RH, Bias WB.
    J Clin Endocrinol Metab; 1987 Nov; 65(5):980-6. PubMed ID: 2822757
    [Abstract] [Full Text] [Related]

  • 9. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype.
    Libber SM, Migeon CJ, Bias WB.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788
    [Abstract] [Full Text] [Related]

  • 10. HLA associations in patients with polycystic ovaries and in patients with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency.
    Hague WM, Adams J, Algar V, Drummond V, Schwarz G, Bottazzo GF, Jacobs HS.
    Clin Endocrinol (Oxf); 1990 Apr; 32(4):407-15. PubMed ID: 2347091
    [Abstract] [Full Text] [Related]

  • 11. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
    Livieri C, Belvedere M, Martinetti M, Beluffi G, Fiori P, Cogliati CR, Goffredo V, Lorini R, Severi F.
    Prog Clin Biol Res; 1985 Apr; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

  • 12. Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?
    Stoner E, Dimartino-Nardi J, Kuhnle U, Levine LS, Oberfield SE, New MI.
    Clin Endocrinol (Oxf); 1986 Jan; 24(1):9-20. PubMed ID: 3486728
    [Abstract] [Full Text] [Related]

  • 13. Detection of heterozygous carriers for 21-hydroxylase deficiency by plasma 21-deoxycortisol measurement.
    Gourmelen M, Gueux B, Pham Huu Trung MT, Fiet J, Raux-Demay MC, Girard F.
    Acta Endocrinol (Copenh); 1987 Dec; 116(4):507-12. PubMed ID: 2827419
    [Abstract] [Full Text] [Related]

  • 14. Basic and clinical aspects of congenital adrenal hyperplasia.
    New MI.
    J Steroid Biochem; 1987 Dec; 27(1-3):1-7. PubMed ID: 3320531
    [Abstract] [Full Text] [Related]

  • 15. '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; 109(3):386-92. PubMed ID: 2992207
    [Abstract] [Full Text] [Related]

  • 16. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Layrisse Z, White C, Gunczler P, Gafaro Valera L, Arias S, Yunis EJ, Alper CA, Awdeh ZL.
    Immunogenetics; 1987 Jul; 25(2):99-103. PubMed ID: 3493216
    [Abstract] [Full Text] [Related]

  • 17. The immunological detection of a 21-OH deficiency mutation HLA supratype.
    Pollack MS, Keenan B, Christiansen FT, Cobain TJ, Dawkins RL, Clayton G.
    Am J Hum Genet; 1986 May; 38(5):688-98. PubMed ID: 3013005
    [Abstract] [Full Text] [Related]

  • 18. Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region.
    Boehm BO, Rosak C, Boehm TL, Kuehnl P, White PC, Schöffling K.
    Mol Biol Med; 1986 Oct; 3(5):437-48. PubMed ID: 2882404
    [Abstract] [Full Text] [Related]

  • 19. Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.
    Lobo RA, Goebelsmann U.
    Am J Obstet Gynecol; 1980 Nov 15; 138(6):720-6. PubMed ID: 6254362
    [Abstract] [Full Text] [Related]

  • 20. [Analysis of the association of HLA-DQ1 alleles with mutation of the 21-hydroxylase gene in patients with congenital adrenal hyperplasia].
    Osinovskaia NS, Ivashchenko TE, Baranov VS.
    Genetika; 2004 Jan 15; 40(1):97-101. PubMed ID: 15027205
    [Abstract] [Full Text] [Related]

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