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Journal Abstract Search

188 related items for PubMed ID: 6286442

  • 1. 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; 16(3):151-9. PubMed ID: 6286442
    [Abstract] [Full Text] [Related]

  • 2. '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]

  • 3. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1981 Dec; 53(6):1193-8. PubMed ID: 6271801
    [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. 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]

  • 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. 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; 50(3):586-9. PubMed ID: 6244328
    [Abstract] [Full Text] [Related]

  • 8. 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 Mar; 458():71-5. PubMed ID: 3879133
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1980 Dec; 51(6):1316-24. PubMed ID: 6449518
    [Abstract] [Full Text] [Related]

  • 11. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.
    New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS.
    J Clin Endocrinol Metab; 1983 Aug; 57(2):320-6. PubMed ID: 6306039
    [Abstract] [Full Text] [Related]

  • 12. HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.
    Pollack MS, Levine LS, O'Neill GJ, Pang S, Lorenzen F, Kohn B, Rondanini GF, Chiumello G, New MI, Dupont B.
    Am J Hum Genet; 1981 Jul; 33(4):540-50. PubMed ID: 6789674
    [Abstract] [Full Text] [Related]

  • 13. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study.
    Kauschansky A, Kaufman H, Zamir R, Elian E.
    Horm Res; 1981 Jul; 14(2):73-8. PubMed ID: 6268517
    [No Abstract] [Full Text] [Related]

  • 14. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
    Stuckey MS, Boyne P, Macdonald WB, Christiansen FT, Houliston JB, Dawkins RL.
    Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
    [Abstract] [Full Text] [Related]

  • 15. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
    Kohn B, Levine LS, Pollack MS, Pang S, Lorenzen F, Levy D, Lerner AJ, Rondanini GF, Dupont B, New MI.
    J Clin Endocrinol Metab; 1982 Nov; 55(5):817-27. PubMed ID: 6288753
    [Abstract] [Full Text] [Related]

  • 16. [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]

  • 17. 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]

  • 18. 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]

  • 19. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
    Migeon CJ, Rosenwaks Z, Lee PA, Urban MD, Bias WB.
    J Clin Endocrinol Metab; 1980 Sep; 51(3):647-9. PubMed ID: 6251108
    [Abstract] [Full Text] [Related]

  • 20. Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I.
    O'Neill GJ, Pollack MS, Yang SY, Levine LS, New MI, Dupont B.
    Transplant Proc; 1979 Dec; 11(4):1713-5. PubMed ID: 316936
    [No Abstract] [Full Text] [Related]

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