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Journal Abstract Search

127 related items for PubMed ID: 6607909

  • 21. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency.
    Peter M.
    Semin Reprod Med; 2002 Aug; 20(3):249-54. PubMed ID: 12428205
    [Abstract] [Full Text] [Related]

  • 22. Prenatal diagnosis of 11beta-hydroxylase deficiency congenital adrenal hyperplasia.
    Rösler A, Leiberman E, Rosenmann A, Ben-Uzilio R, Weidenfeld J.
    J Clin Endocrinol Metab; 1979 Oct; 49(4):546-51. PubMed ID: 314453
    [Abstract] [Full Text] [Related]

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

  • 24. Diagnosis of adrenal cortical dysfunction by liquid chromatography-tandem mass spectrometry.
    Kao PC, Machacek DA, Magera MJ, Lacey JM, Rinaldo P.
    Ann Clin Lab Sci; 2001 Apr; 31(2):199-204. PubMed ID: 11337910
    [Abstract] [Full Text] [Related]

  • 25. Difficulties in the diagnosis of congenital adrenal hyperplasia in early infancy: the 11 beta-hydroxylase defect.
    Honour JW, Anderson JM, Shackleton CH.
    Acta Endocrinol (Copenh); 1983 May; 103(1):101-9. PubMed ID: 6602444
    [Abstract] [Full Text] [Related]

  • 26. [Congenital virilization in a newborn girl of a mother with adrenogenital syndrome due to 21-hydroxylase deficiency].
    Ferrante L.
    Minerva Pediatr; 1976 Jun 23; 28(22):1443-4. PubMed ID: 986003
    [No Abstract] [Full Text] [Related]

  • 27. Congenital adrenal hyperplasia: problems with developmental anomalies of the external genitalia and sex assignment.
    Al-Maghribi H.
    Saudi J Kidney Dis Transpl; 2007 Sep 23; 18(3):405-13. PubMed ID: 17679754
    [Abstract] [Full Text] [Related]

  • 28. [Current concepts in the treatment of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    David M, Bertrand J, Kemlin I, François R.
    Pediatrie; 1981 Mar 23; 36(2):161-6. PubMed ID: 6972030
    [No Abstract] [Full Text] [Related]

  • 29. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Mar 23; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 30. Gynecomastia with congenital virilizing adrenal hyperplasia (11-beta-hydroxylase deficiency).
    Maclaren NK, Migeon CJ, Raiti S.
    J Pediatr; 1975 Apr 23; 86(4):579-81. PubMed ID: 123956
    [No Abstract] [Full Text] [Related]

  • 31. Growth and pubertal development in patients with congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency.
    Hochberg Z, Schechter J, Benderly A, Leiberman E, Rosler A.
    Am J Dis Child; 1985 Aug 23; 139(8):771-6. PubMed ID: 3875277
    [Abstract] [Full Text] [Related]

  • 32. [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; 1985 Aug 23; 56(47-68):1975-8. PubMed ID: 6256909
    [Abstract] [Full Text] [Related]

  • 33. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A, Stivel M, Zamir R, Kaufman H, Pertzelan A, Laron Z.
    Isr J Med Sci; 1982 Jul 23; 18(7):763-8. PubMed ID: 6980865
    [Abstract] [Full Text] [Related]

  • 34. [Congenital virilizing adrenal hyperplasia due to 11 -beta-hydroxylase deficiency. Study of 11 cases (author's transl)].
    Dunand A, Roger M, Chaussain JL, Nocton F, Job JC.
    Ann Pediatr (Paris); 1981 Mar 23; 28(3):179-84. PubMed ID: 7224566
    [No Abstract] [Full Text] [Related]

  • 35. The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern.
    van der Ploeg KR, Wolthers BG, Nagel GT, Volmer M, Drayer NM.
    Clin Chim Acta; 1982 Apr 23; 120(3):341-53. PubMed ID: 6978779
    [Abstract] [Full Text] [Related]

  • 36. [Case of salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency and a short stature caused by early closure of epiphyseal lines in spite of steroid replacement therapy].
    Kondo T, Ueda K, Saito H, Horiuchi Y.
    Horumon To Rinsho; 1983 Jul 23; 31(7):637-43. PubMed ID: 6605823
    [No Abstract] [Full Text] [Related]

  • 37. [Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood].
    Mackenroth T.
    Internist (Berl); 1986 Apr 23; 27(4):274-8. PubMed ID: 3519519
    [No Abstract] [Full Text] [Related]

  • 38. Apparent double defect in C11 beta and C21-steroid hydroxylation in congenital adrenal hyperplasia.
    Finkelstein M, Litvin Y, Mizrachi Y, Neiman G, Rösler A.
    J Steroid Biochem; 1983 Jul 23; 19(1B):675-81. PubMed ID: 6310249
    [Abstract] [Full Text] [Related]

  • 39. Steroid spectrum in human urine as revealed by gas chromatography V. Identification and quantitation of 3 alpha, 20 alpha-dihydroxy-5-beta pregnan-11-one (11-keto-pregnanediol) during different stages of development in children with C/21 hydroxylase deficiency.
    Kecskés L, Czira G.
    Acta Biochim Biophys Acad Sci Hung; 1981 Jul 23; 16(3-4):179-88. PubMed ID: 6982583
    [Abstract] [Full Text] [Related]

  • 40. [Congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency].
    Dumić M.
    Lijec Vjesn; 1996 Mar 23; 118 Suppl 1():13-6. PubMed ID: 8759401
    [Abstract] [Full Text] [Related]

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