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Journal Abstract Search

128 related items for PubMed ID: 3265870

  • 21. 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; 22(3):363-9. PubMed ID: 3990286
    [Abstract] [Full Text] [Related]

  • 22. Metabotypes of congenital adrenal hyperplasia in infants determined by gas chromatography-mass spectrometry in spot urine.
    Kamrath C, Friedrich C, Hartmann MF, Wudy SA.
    J Steroid Biochem Mol Biol; 2023 Jul; 231():106304. PubMed ID: 36990162
    [Abstract] [Full Text] [Related]

  • 23. Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients.
    Zachmann M, Tassinari D, Prader A.
    J Clin Endocrinol Metab; 1983 Feb; 56(2):222-9. PubMed ID: 6296182
    [Abstract] [Full Text] [Related]

  • 24. Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 3. Characterization, using GC-MS and GC-MS/MS, of androstanes and androstenes.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2012 Nov; 77(13):1487-501. PubMed ID: 22974828
    [Abstract] [Full Text] [Related]

  • 25. Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 2. Characterization, using GC-MS and GC-MS/MS, of pregnanes and pregnenes with an oxo- group on the A- or B-ring.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2012 Apr; 77(5):382-93. PubMed ID: 22210448
    [Abstract] [Full Text] [Related]

  • 26. Evidence against significant 19-nor-deoxycorticosterone production in patients with 17 alpha-hydroxylase deficiency.
    Shackleton CH.
    Clin Exp Hypertens A; 1982 Apr; 4(9-10):1529-39. PubMed ID: 6982794
    [Abstract] [Full Text] [Related]

  • 27. Significance of 3alpha, 17 alpha-dihydroxy-5beta-pregnane-20-one in the diagnosis of congenital adrenal hyperplasia.
    Kecskés L, Tényi I, Németh M, Juricskay Z, Temesi M.
    Endokrinologie; 1975 Sep; 66(1):94-9. PubMed ID: 1225520
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. The early recognition of the 21-hydroxylase deficiency variety of congenital adrenal hyperplasia.
    Steen G, Tas AC, Ten Noever De Brauw MC, Drayer NM, Wolthers BG.
    Clin Chim Acta; 1980 Aug 04; 105(2):213-24. PubMed ID: 6931002
    [Abstract] [Full Text] [Related]

  • 30. Steroids excreted in urine by neonates with 21-hydroxylase deficiency: characterization, using GC-MS and GC-MS/MS, of the D-ring and side chain structure of pregnanes and pregnenes.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2010 Jan 04; 75(1):34-52. PubMed ID: 19799922
    [Abstract] [Full Text] [Related]

  • 31. New identified 15 beta-hydroxylated 21-deoxy-pregnanes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Kraan GP, Wolthers BG, van der Molen JC, Nagel GT, Drayer NM, Joannou GE.
    J Steroid Biochem Mol Biol; 1993 May 04; 45(5):421-34. PubMed ID: 8499349
    [Abstract] [Full Text] [Related]

  • 32. [An analysis and identification of urinary steroids in normal people and patients with 21-hydroxylase deficiency and urinary excretion patterns].
    Mizumoto T, Kondo S, Yamasaki S.
    Nihon Naibunpi Gakkai Zasshi; 1984 Feb 20; 60(2):131-46. PubMed ID: 6609847
    [Abstract] [Full Text] [Related]

  • 33. A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency.
    Shackleton CH, Homoki J, Taylor NF.
    Steroids; 1987 Feb 20; 49(4-5):295-311. PubMed ID: 3502660
    [Abstract] [Full Text] [Related]

  • 34. 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 20; 19(1B):645-53. PubMed ID: 6887889
    [Abstract] [Full Text] [Related]

  • 35. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 36. A chemiluminescent method for the measurement of pregnanetriol-3 alpha-glucuronide in human diluted urine.
    Pinzani P, Magini A, Franceschetti F, Messeri G, Pazzagli M.
    J Biolumin Chemilumin; 1989 Jul 07; 4(1):580-6. PubMed ID: 2552757
    [Abstract] [Full Text] [Related]

  • 37. Pregnenolone, 17-OH-pregnenolone, and testosterone in plasma of patients with congenital adrenal hyperplasia.
    McKenna TJ, Jennings AS, Liddle GW, Burr IM.
    J Clin Endocrinol Metab; 1976 May 07; 42(5):918-25. PubMed ID: 178685
    [Abstract] [Full Text] [Related]

  • 38. Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 4. Characterization, using GC-MS and GC-MS/MS, of 11oxo-pregnanes and 11oxo-pregnenes.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2013 May 07; 78(5):468-75. PubMed ID: 23454217
    [Abstract] [Full Text] [Related]

  • 39. A test for heterozygocity of 21-hydroxylase deficiency: preliminary report.
    Homoki J, Teller WM, Fazekas AT.
    Hum Genet; 1976 Apr 15; 32(1):35-41. PubMed ID: 177352
    [Abstract] [Full Text] [Related]

  • 40. Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.
    Homma K, Hasegawa T, Takeshita E, Watanabe K, Anzo M, Toyoura T, Jinno K, Ohashi T, Hamajima T, Takahashi Y, Takahashi T, Matsuo N.
    J Clin Endocrinol Metab; 2004 Dec 15; 89(12):6087-91. PubMed ID: 15579762
    [Abstract] [Full Text] [Related]

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