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Journal Abstract Search

119 related items for PubMed ID: 6965821

  • 21. Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women.
    Pang SY, Lerner AJ, Stoner E, Levine LS, Oberfield SE, Engel I, New MI.
    J Clin Endocrinol Metab; 1985 Mar; 60(3):428-39. PubMed ID: 2982896
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. 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]

  • 24. The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women.
    Chetkowski RJ, DeFazio J, Shamonki I, Judd HL, Chang RJ.
    J Clin Endocrinol Metab; 1984 Apr; 58(4):595-8. PubMed ID: 6321532
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. Clinical and endocrinological aspects of 21-hydroxylase deficiency.
    New MI.
    Ann N Y Acad Sci; 1985 Nov; 458():1-27. PubMed ID: 3911845
    [No Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. 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]

  • 29. Effects of continued adrenocorticotropin stimulation on the mineralocorticoid hormones in classical and nonclassical simple virilizing types of 21-hydroxylase deficiency.
    Kater CE, Biglieri EG, Wajchenberg B.
    J Clin Endocrinol Metab; 1985 Jun; 60(6):1057-62. PubMed ID: 2987285
    [Abstract] [Full Text] [Related]

  • 30. [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 Jun; 43(3):203-11. PubMed ID: 6984316
    [Abstract] [Full Text] [Related]

  • 31. Adrenal androgen hyperresponsiveness to adrenocorticotropin in women with acne and/or hirsutism: adrenal enzyme defects and exaggerated adrenarche.
    Lucky AW, Rosenfield RL, McGuire J, Rudy S, Helke J.
    J Clin Endocrinol Metab; 1986 May; 62(5):840-8. PubMed ID: 3007557
    [Abstract] [Full Text] [Related]

  • 32. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 May; 43(1):3-14. PubMed ID: 6982657
    [Abstract] [Full Text] [Related]

  • 33. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.
    Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF.
    Pediatrics; 1983 Nov; 72(5):690-5. PubMed ID: 6314235
    [Abstract] [Full Text] [Related]

  • 34. 17 alpha-hydroxylase deficiency: mineralocorticoid hormone profiles in an affected family.
    D'Armiento M, Reda G, Kater C, Shackleton CH, Biglieri EG.
    J Clin Endocrinol Metab; 1983 Apr; 56(4):697-701. PubMed ID: 6300162
    [Abstract] [Full Text] [Related]

  • 35. [Late diagnosis hyperandrogenism due to adrenal enzyme deficiency (author's transl)].
    Hazard J, Guilhaume B, Requeda E, Perlemuter L, Cenac A, Bernheim R.
    Sem Hop; 1983 Apr; 56(47-68):1975-8. PubMed ID: 6256909
    [Abstract] [Full Text] [Related]

  • 36. The biochemical basis for genotyping 21-hydroxylase deficiency.
    New MI, Dupont B, Pollack MS, Levine LS.
    Hum Genet; 1981 Apr; 58(1):123-7. PubMed ID: 6269988
    [Abstract] [Full Text] [Related]

  • 37. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984 Apr; 41(7):483-5. PubMed ID: 6333857
    [Abstract] [Full Text] [Related]

  • 38. 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; 67(1):154-60. PubMed ID: 2837498
    [Abstract] [Full Text] [Related]

  • 39.
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    [No Abstract] [Full Text] [Related]

  • 40. [Adrenogenital syndrome. I. Introduction, enzymology and heredity].
    Koppens PF, Hoogenboezem T, Degenhart HJ.
    Tijdschr Kindergeneeskd; 1989 Aug; 57(4):129-35. PubMed ID: 2678599
    [Abstract] [Full Text] [Related]

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