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Journal Abstract Search

191 related items for PubMed ID: 6290362

  • 41. [HLA haplotypes in congenital adrenal hyperplasia (21-hydroxylase deficiency].
    González-Díaz JP, González T, González-Espinosa C, Gantes M, Santisteban M, Bustad S.
    An Esp Pediatr; 1984 Oct 31; 21(6):583-6. PubMed ID: 6335362
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  • 42. 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 Oct 31; 25(2):99-103. PubMed ID: 3493216
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  • 43. Recent advances in 21-hydroxylase deficiency.
    New MI, Levine LS.
    Annu Rev Med; 1984 Oct 31; 35():649-63. PubMed ID: 6372675
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  • 45. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
    Speiser PW, New MI, White PC.
    N Engl J Med; 1988 Jul 07; 319(1):19-23. PubMed ID: 3260007
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  • 46. The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency.
    Feuillan P, Pang S, Schürmeyer T, Avgerinos PC, Chrousos GP.
    J Clin Endocrinol Metab; 1988 Jul 07; 67(1):154-60. PubMed ID: 2837498
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  • 47. 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 07; 68(3):542-7. PubMed ID: 2537337
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  • 48. [Hormonal profile and HLA typing of adult subjects from 7 families with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Bercovici JP, Tater D, Khoury S, Le Fur JM, Saleun JP, Nahoul K, Scholler R.
    Ann Endocrinol (Paris); 1982 Mar 07; 43(3):203-11. PubMed ID: 6984316
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  • 50. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar 07; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 51. HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population.
    Couillin P, Rappaport R, Kuttenn F, Canlorbe P, Hors J, Marcelli-Barge A, Feingold J, Grisard MC, Boué J, Boué A.
    Tissue Antigens; 1982 Feb 07; 19(2):100-7. PubMed ID: 6980498
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  • 53. Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency.
    Dewailly D, Vantyghem-Haudiquet MC, Sainsard C, Buvat J, Cappoen JP, Ardaens K, Racadot A, Lefebvre J, Fossati P.
    J Clin Endocrinol Metab; 1986 Aug 07; 63(2):418-23. PubMed ID: 3013919
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  • 54. Screening heterozygotes for 21-hydroxylase deficiency among hirsute women: lack of utility of the adrenocorticotropin hormone test.
    Dewailly D, Vantyghem MC, Lemaire C, Dufosse F, Racadot A, Fossati P.
    Fertil Steril; 1988 Aug 07; 50(2):228-32. PubMed ID: 2840308
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  • 55. 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 07; 38(5):688-98. PubMed ID: 3013005
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  • 58. Nonclassic adrenal hyperplasia due to 21-hydroxylase deficiency.
    Drucker S, New MI.
    Pediatr Clin North Am; 1987 Aug 07; 34(4):1067-81. PubMed ID: 3302893
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  • 59. 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 07; 61(1):89-97. PubMed ID: 3873469
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  • 60. 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 Jul 07; 458():71-5. PubMed ID: 3879133
    [Abstract] [Full Text] [Related]

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