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Journal Abstract Search

131 related items for PubMed ID: 6602444

  • 1. 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]

  • 2. 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; 19(1B):675-81. PubMed ID: 6310249
    [Abstract] [Full Text] [Related]

  • 3. 11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
    Rösler A, Weshler N, Leiberman E, Hochberg Z, Weidenfeld J, Sack J, Chemke J.
    J Clin Endocrinol Metab; 1988 Apr; 66(4):830-8. PubMed ID: 3346360
    [Abstract] [Full Text] [Related]

  • 4. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
    Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

  • 5. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 6. Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine.
    Hughes IA, Arisaka O, Perry LA, Honour JW.
    Acta Endocrinol (Copenh); 1986 Mar; 111(3):349-54. PubMed ID: 3515819
    [Abstract] [Full Text] [Related]

  • 7. Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroids.
    Yong AB, Pitt JJ, Montalto J, Davies HE, Warne GL, Connelly JF.
    Aust Paediatr J; 1988 Oct; 24(5):280-5. PubMed ID: 3265870
    [Abstract] [Full Text] [Related]

  • 8. Identification of 15 beta-hydroxylated C21 steroids in the neo-natal period: the role of 3 alpha,15 beta,17 alpha-trihydroxy-5 beta-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (CAH) due to a 21-hydroxylase deficiency.
    Joannou GE.
    J Steroid Biochem; 1981 Sep; 14(9):901-12. PubMed ID: 6975400
    [No Abstract] [Full Text] [Related]

  • 9. A pilot study for neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase and 11-beta-hydroxylase deficiency in Campania region.
    Valentino R, Tommaselli AP, Rossi R, Lombardi G, Varrone S.
    J Endocrinol Invest; 1990 Mar; 13(3):221-5. PubMed ID: 2365957
    [Abstract] [Full Text] [Related]

  • 10. Increased urinary excretion of total 16 alpha-hydroxypregnenolone in newborn infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Homoki J, Teller WM.
    Klin Wochenschr; 1982 Apr 15; 60(8):407-10. PubMed ID: 6980322
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 49(4):546-51. PubMed ID: 314453
    [Abstract] [Full Text] [Related]

  • 12. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Oct 15; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 13. A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency.
    Shackleton CH, Homoki J, Taylor NF.
    Steroids; 1987 Oct 15; 49(4-5):295-311. PubMed ID: 3502660
    [Abstract] [Full Text] [Related]

  • 14. Sex reassignment in a girl with 11 beta-hydroxylase deficiency.
    Bistritzer T, Sack J, Eshkol A, Zur H, Katznelson D.
    Isr J Med Sci; 1984 Jan 15; 20(1):55-8. PubMed ID: 6607909
    [Abstract] [Full Text] [Related]

  • 15. [Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].
    Bouchard M, Forest MG, David M, Dechaud H, Juif JG.
    Pediatrie; 1989 Jan 15; 44(8):637-40. PubMed ID: 2622705
    [Abstract] [Full Text] [Related]

  • 16. Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of life.
    Shackleton CH.
    Clin Chim Acta; 1976 Mar 15; 67(3):287-98. PubMed ID: 1261045
    [Abstract] [Full Text] [Related]

  • 17. Clinical and endocrinological aspects of 21-hydroxylase deficiency.
    New MI.
    Ann N Y Acad Sci; 1985 Mar 15; 458():1-27. PubMed ID: 3911845
    [No Abstract] [Full Text] [Related]

  • 18. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].
    Lambotte C.
    Rev Med Liege; 1986 Jan 15; 41(2):37-44. PubMed ID: 3006204
    [No Abstract] [Full Text] [Related]

  • 19. Congenital adrenal hyperplasia due to combined 21- and 11 beta-hydroxylase deficiency.
    Penny R, Vecsei P.
    J Endocrinol Invest; 1989 Nov 15; 12(10):723-8. PubMed ID: 2614011
    [Abstract] [Full Text] [Related]

  • 20. Diagnosis of homozygosity and heterozygosity in congenital adrenal hyperplasia (CAH) and control of treatment.
    Knorr D, Bidlingmaier F, Höller W, Kuhnle U.
    J Steroid Biochem; 1983 Jul 15; 19(1B):645-53. PubMed ID: 6887889
    [Abstract] [Full Text] [Related]

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