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Journal Abstract Search

120 related items for PubMed ID: 6121730

  • 21. [17 alpha-hydroxylase deficiency and 5 alpha-reductase deficiency].
    Yoshida H, Shimizu N.
    Nihon Rinsho; 1979 Jun 10; 37(6):1253-9. PubMed ID: 384051
    [No Abstract] [Full Text] [Related]

  • 22. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
    Waldhäusl W, Herkner K, Nowotny P, Bratusch-Marrain P.
    J Clin Endocrinol Metab; 1978 Feb 10; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 23. Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign.
    Çamtosun E, Şıklar Z, Ceylaner S, Kocaay P, Berberoğlu M.
    J Clin Res Pediatr Endocrinol; 2017 Jun 01; 9(2):163-167. PubMed ID: 28008861
    [Abstract] [Full Text] [Related]

  • 24. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar 01; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 25. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984 Mar 01; 41(7):483-5. PubMed ID: 6333857
    [Abstract] [Full Text] [Related]

  • 26. Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase.
    Roger M, Merceron RE, Girard F, Canlorbe P, Dehennin L, Konopka P, Seneze J, Toublanc JE.
    Horm Res; 1982 Mar 01; 16(1):23-31. PubMed ID: 6279481
    [Abstract] [Full Text] [Related]

  • 27. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Mar 01; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 28. Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Passarge E.
    Indian J Pediatr; 1988 Mar 01; 55(4):472-5. PubMed ID: 3262582
    [No Abstract] [Full Text] [Related]

  • 29. 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 01; 28(6):657-64. PubMed ID: 2855412
    [Abstract] [Full Text] [Related]

  • 30. [Congenital virilizing adrenal hyperplasia due to 11 beta-hydroxylase deficiency. Study of eleven cases (author's transl)].
    Dunand A, Roger M, Chaussain JL, Nocton F, Job JC.
    Sem Hop; 1988 Jun 01; 57(33-36):1392-7. PubMed ID: 6270798
    [Abstract] [Full Text] [Related]

  • 31. Diagnosis and natural history of 17-hydroxylase deficiency in a newborn male.
    Dean HJ, Shackleton CH, Winter JS.
    J Clin Endocrinol Metab; 1984 Sep 01; 59(3):513-20. PubMed ID: 6086702
    [Abstract] [Full Text] [Related]

  • 32. Adult-onset familial adrenal 21-hydroxylase deficiency.
    Blankstein J, Faiman C, Reyes FI, Schroeder ML, Winter JS.
    Am J Med; 1980 Mar 01; 68(3):441-8. PubMed ID: 6965821
    [Abstract] [Full Text] [Related]

  • 33. 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 01; 7(2):89-92. PubMed ID: 6327799
    [Abstract] [Full Text] [Related]

  • 34. [A case of congenital adrenogenital syndrome].
    Sumiya H, Kawamura K, Kataumi Z, Fuse H, Ito H, Shimazaki J.
    Hinyokika Kiyo; 1985 Aug 01; 31(8):1433-9. PubMed ID: 3878668
    [Abstract] [Full Text] [Related]

  • 35. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG, Brykova EK, Bakharev VA.
    Akush Ginekol (Mosk); 1990 Jan 01; (1):10-4. PubMed ID: 2353725
    [No Abstract] [Full Text] [Related]

  • 36. The biochemical basis for genotyping 21-hydroxylase deficiency.
    New MI, Dupont B, Pollack MS, Levine LS.
    Hum Genet; 1981 Jan 01; 58(1):123-7. PubMed ID: 6269988
    [Abstract] [Full Text] [Related]

  • 37. [Adrenal enzyme defects and intersexuality].
    Schlaghecke R, Kornely E.
    Gynakologe; 1995 Feb 01; 28(1):27-32. PubMed ID: 7705712
    [No Abstract] [Full Text] [Related]

  • 38. Clinical and endocrinological aspects of 21-hydroxylase deficiency.
    New MI.
    Ann N Y Acad Sci; 1985 Feb 01; 458():1-27. PubMed ID: 3911845
    [No Abstract] [Full Text] [Related]

  • 39. [Report on 3 cases of 17 alpha-hydroxylase deficiency].
    Zhang ZJ.
    Zhonghua Nei Ke Za Zhi; 1983 Sep 01; 22(9):565-7. PubMed ID: 6606541
    [No Abstract] [Full Text] [Related]

  • 40. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
    Chrousos GP, Loriaux DL, Mann D, Cutler GB.
    Horm Res; 1982 Sep 01; 16(4):193-200. PubMed ID: 6290362
    [Abstract] [Full Text] [Related]

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