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Journal Abstract Search

122 related items for PubMed ID: 221633

  • 1. Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Gutai JP, Lee PA, Johnsonbaugh RE, Gareis F, Urban MD, Migeon CJ.
    J Pediatr; 1979 May; 94(5):770-2. PubMed ID: 221633
    [No Abstract] [Full Text] [Related]

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  • 3. 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 May; 14(2):73-8. PubMed ID: 6268517
    [No Abstract] [Full Text] [Related]

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  • 5. Identification of heterozygote carriers of congenital adrenal hyperplasia by radioimmunoassay of serum 17-OH progesterone.
    Krensky AM, Bongiovanni AM, Marino J, Parks J, Tenore A.
    J Pediatr; 1977 Jun; 90(6):930-3. PubMed ID: 859065
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  • 6. Partial adrenocortical hydroxylase deficiency syndrome in infertile women.
    Loran Z, Roitman A, Pollack MS, Dupont B.
    Fertil Steril; 1980 Jul; 34(1):76. PubMed ID: 6249647
    [No Abstract] [Full Text] [Related]

  • 7. The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasia.
    Gutai JP, Kowarski AA, Migeon CJ.
    J Pediatr; 1977 Jun; 90(6):924-9. PubMed ID: 192874
    [Abstract] [Full Text] [Related]

  • 8. No linkage between HLA and congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency.
    Brautbar C, Rösler A, Landau H, Cohen I, Nelken D, Cohen T, Levine C, Sack J, Benderli A, Moses S, Lieberman E, Dupont B, Levine LS, New MI.
    N Engl J Med; 1979 Jan 25; 300(4):205-6. PubMed ID: 759866
    [No Abstract] [Full Text] [Related]

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  • 10. Evidence for partial 21-hydroxylase deficiency among heterozygote carriers of congenital adrenal hyperplasia.
    Lee PA, Gareis JF.
    J Clin Endocrinol Metab; 1975 Aug 25; 41(2):415-8. PubMed ID: 169282
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  • 12. 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 25; 50(3):586-9. PubMed ID: 6244328
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  • 14. 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 25; 116(4):507-12. PubMed ID: 2827419
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  • 15. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Khandekar S, Lata V, Dash RJ.
    Indian J Med Res; 1990 Apr 25; 92():79-82. PubMed ID: 2164496
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  • 17. Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lorenzen F, Pang S, New M, Pollack M, Oberfield S, Dupont B, Chow D, Schneider B, Levine L.
    J Clin Endocrinol Metab; 1980 Mar 25; 50(3):572-7. PubMed ID: 6244326
    [No Abstract] [Full Text] [Related]

  • 18. Circadian variation of plasma 17-hydroxyprogesterone among heterozygotic carriers of 21-hydroxylase deficiency (salt-losing form).
    Urban MD, Migeon CJ, Lee PA.
    Horm Res; 1986 Mar 25; 23(2):74-7. PubMed ID: 3484712
    [Abstract] [Full Text] [Related]

  • 19. [Plasmatic 17-alpha-hydroxyprogesterone in congenital adrenal hyperplasia due to 21 hydroxylase deficiency, treated and untreated].
    Loras B, Roux H, Audi-Parera L, David M, Bertrand J.
    Biomedicine; 1974 Jul 25; 21(7):317-22. PubMed ID: 4373095
    [No Abstract] [Full Text] [Related]

  • 20. Heterozygotes for 17 alpha-hydroxylase deficiency can be detected with a short ACTH test.
    Wit JM, van Roermund HP, Oostdijk W, Benraad TJ, Thijssen JH, Boer P, Jansen M, Spit M, van den Brande JL.
    Clin Endocrinol (Oxf); 1988 Jun 25; 28(6):657-64. PubMed ID: 2855412
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