These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

191 related items for PubMed ID: 6290362

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. 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]

  • 24. 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]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. 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]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. 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 15; 116(4):507-12. PubMed ID: 2827419
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).
    Carmina E, Gagliano AM, Rosato F, Maggiore M, Jannì A.
    J Endocrinol Invest; 1984 Apr 15; 7(2):89-92. PubMed ID: 6327799
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. 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 15; 33(4):540-50. PubMed ID: 6789674
    [Abstract] [Full Text] [Related]

  • 37. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Couillin P.
    Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Late onset adrenal hyperplasia in a group of Irish females who presented with hirsutism, irregular menses and/or cystic acne.
    McLaughlin B, Barrett P, Finch T, Devlin JG.
    Clin Endocrinol (Oxf); 1990 Jan 21; 32(1):57-64. PubMed ID: 2139596
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.