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Journal Abstract Search

189 related items for PubMed ID: 1728539

  • 1. Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Homoki J, Sólyom J, Wachter U, Teller WM.
    Eur J Pediatr; 1992 Jan; 151(1):24-8. PubMed ID: 1728539
    [Abstract] [Full Text] [Related]

  • 2. Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.
    Homoki J, Solyom J, Teller WM.
    Eur J Pediatr; 1988 Apr; 147(3):257-62. PubMed ID: 3260557
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Modified-Release and Conventional Glucocorticoids and Diurnal Androgen Excretion in Congenital Adrenal Hyperplasia.
    Jones CM, Mallappa A, Reisch N, Nikolaou N, Krone N, Hughes BA, O'Neil DM, Whitaker MJ, Tomlinson JW, Storbeck KH, Merke DP, Ross RJ, Arlt W.
    J Clin Endocrinol Metab; 2017 Jun 01; 102(6):1797-1806. PubMed ID: 27845856
    [Abstract] [Full Text] [Related]

  • 5. The application of a serum 17OH-progesterone radioimmunoassay to the diagnosis and management of congenital adrenal hyperplasia.
    Hughes IA, Winter JS.
    J Pediatr; 1976 May 01; 88(5):766-73. PubMed ID: 1271137
    [Abstract] [Full Text] [Related]

  • 6. [Determination of urinary 17 alpha-hydroxyprogesterone excretion using ELISA--evaluation of normal subjects and patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Shibata Y.
    Nihon Naibunpi Gakkai Zasshi; 1991 Aug 20; 67(8):819-39. PubMed ID: 1813324
    [Abstract] [Full Text] [Related]

  • 7. Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: effect on midgestational amniotic fluid steroid levels.
    Dörr HG, Sippell WG.
    J Clin Endocrinol Metab; 1993 Jan 20; 76(1):117-20. PubMed ID: 8421074
    [Abstract] [Full Text] [Related]

  • 8. Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening.
    Sarafoglou K, Lorentz CP, Otten N, Oetting WS, Grebe SK.
    Clin Genet; 2012 Jul 20; 82(1):64-70. PubMed ID: 21534945
    [Abstract] [Full Text] [Related]

  • 9. Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency. Results of a multicenter study.
    Hargitai G, Sólyom J, Battelino T, Lebl J, Pribilincová Z, Hauspie R, Kovács J, Waldhauser F, Frisch H, MEWPE-CAH Study Group.
    Horm Res; 2001 Jul 20; 55(4):161-71. PubMed ID: 11598369
    [Abstract] [Full Text] [Related]

  • 10. [Reevaluation of recalled infants by neonatal mass screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Diagnostic value of pregnanetriolone in a single urine specimen using glass capillary gas chromatography].
    Hikita Y.
    Nihon Naibunpi Gakkai Zasshi; 1985 Mar 20; 61(3):197-219. PubMed ID: 3874793
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. A possible defect in the inter-conversion between cortisone and cortisol in prepubertal patients with congenital adrenal hyperplasia receiving cortisone acetate therapy.
    Whorwood CB, Warne GL.
    J Steroid Biochem Mol Biol; 1991 Oct 23; 39(4A):461-70. PubMed ID: 1911435
    [Abstract] [Full Text] [Related]

  • 13. Growth pattern of untreated boys with simple virilizing congenital adrenal hyperplasia indicates relative androgen insensitivity during the first six months of life.
    Bonfig W, Schwarz HP.
    Horm Res Paediatr; 2011 Oct 23; 75(4):264-8. PubMed ID: 21196707
    [Abstract] [Full Text] [Related]

  • 14. Urinary excretion of pregnanetriol and 5 -pregnenetriol in two forms of congenital adrenal hyperplasia.
    Bongiovanni AM, Eberlein WR, Moshang T.
    J Clin Invest; 1971 Dec 23; 50(12):2751-4. PubMed ID: 5129323
    [Abstract] [Full Text] [Related]

  • 15. Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia between 1995 and 2006.
    Dumic K, Krnic N, Skrabic V, Stipancic G, Cvijovic K, Kusec V, Stingl K.
    Horm Res; 2009 Dec 23; 72(4):247-51. PubMed ID: 19786796
    [Abstract] [Full Text] [Related]

  • 16. The urinary steroidome of treated children with classic 21-hydroxylase deficiency.
    Kamrath C, Wettstaedt L, Boettcher C, Hartmann MF, Wudy SA.
    J Steroid Biochem Mol Biol; 2017 Jan 23; 165(Pt B):396-406. PubMed ID: 27544322
    [Abstract] [Full Text] [Related]

  • 17. Androgen excess is due to elevated 11-oxygenated androgens in treated children with congenital adrenal hyperplasia.
    Kamrath C, Wettstaedt L, Boettcher C, Hartmann MF, Wudy SA.
    J Steroid Biochem Mol Biol; 2018 Apr 23; 178():221-228. PubMed ID: 29277706
    [Abstract] [Full Text] [Related]

  • 18. Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia.
    Vierhapper H, Nowotny P, Waldhäusl W, Frisch H.
    J Steroid Biochem; 1985 Mar 23; 22(3):363-9. PubMed ID: 3990286
    [Abstract] [Full Text] [Related]

  • 19. 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 23; 66(4):830-8. PubMed ID: 3346360
    [Abstract] [Full Text] [Related]

  • 20. 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 23; 24(5):280-5. PubMed ID: 3265870
    [Abstract] [Full Text] [Related]

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