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Journal Abstract Search

214 related items for PubMed ID: 6278806

  • 1. Steroid spectrum in human urine as revealed by gas chromatography. IV. Changes in the exception of 16-oxygenated neutral steroids by children with 21-hydroxylase deficiency during different stages of development.
    Kecskés L, Juricskay Z, Kosztoláni G, Szécsényi M.
    Acta Biochim Biophys Acad Sci Hung; 1981; 16(1-2):57-75. PubMed ID: 6278806
    [No Abstract] [Full Text] [Related]

  • 2. 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; 16(3-4):179-88. PubMed ID: 6982583
    [Abstract] [Full Text] [Related]

  • 3. Dynamics of adrenal steroidogenesis in childhood: changes in the excretion of 16-oxygenated- and 11-oxygenated-steroids by 21-hydroxylase deficient children at various ages.
    Kecskés L.
    Endokrinologie; 1982 Oct; 80(2):151-7. PubMed ID: 6297879
    [Abstract] [Full Text] [Related]

  • 4. Application of urinary steroid profiling obtained with capillary column gas chromatography for diagnosis of adrenal disorders in children.
    Małunowicz EM, Gajewska D, Daniewski M, Mielniczuk Z, Filipek M, Romer TE.
    Endokrynol Pol; 1987 Oct; 38(1):65-78. PubMed ID: 3428234
    [No Abstract] [Full Text] [Related]

  • 5. 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; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 6. [Various aspects of steroidogenesis in congenital adrenogenital syndrome with or without salt loss (determination of the urinary excretion of aldosterone, androsterone, etiocholanolone, dehydroisoandrosterone, 17-hydroxy-11-desoxycorticosterone, pregnanediol and pregnanetriol)].
    Cacciari E, Dallera L, Tassoni P, Cicognani A, Miano A.
    Minerva Pediatr; 1969 May 26; 21(21):937-42. PubMed ID: 4247542
    [No Abstract] [Full Text] [Related]

  • 7. Steroid excretion in urine during suppression and stimulation of adrenals in the 17 alpha-hydroxylase deficiency syndrome.
    Honour J, Millar G, Roitman E, Shackleton C.
    J Clin Endocrinol Metab; 1981 May 26; 52(5):1039-42. PubMed ID: 6262355
    [Abstract] [Full Text] [Related]

  • 8. [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; 1981 May 26; 57(33-36):1392-7. PubMed ID: 6270798
    [Abstract] [Full Text] [Related]

  • 9. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers].
    Dumić M, Plavsić V, Brkljacić L, Sarnavka V, Mardesić D, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Apr 26; 105(4):145-9. PubMed ID: 6602259
    [No Abstract] [Full Text] [Related]

  • 10. 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 26; 24(5):280-5. PubMed ID: 3265870
    [Abstract] [Full Text] [Related]

  • 11. A female pseudohermaphrodite with salt losing congenital adrenal hyperplasia as the result of 21--beta--OH deficiency.
    Preeyasombat C, Siripoonya P, Tejavej A, Pitchayayothin N.
    J Med Assoc Thai; 1975 Mar 26; 58(3):61-9. PubMed ID: 1127377
    [No Abstract] [Full Text] [Related]

  • 12. [Congenital adrenogenital syndrome due to 21-hydroxylase deficiency. Pathogenesis, clinical picture, and deliberations over better therapy].
    von Schnakenburg K.
    Med Welt; 1977 Sep 09; 28(36):1415-22. PubMed ID: 904447
    [No Abstract] [Full Text] [Related]

  • 13. Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lorenzen F, Pang S, New M, Pollack M, Oberfield S, Dupont B, Chow D, Schneider B, Levine L.
    J Clin Endocrinol Metab; 1980 Mar 09; 50(3):572-7. PubMed ID: 6244326
    [No Abstract] [Full Text] [Related]

  • 14. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
    Pediatrics; 1980 Apr 09; 65(4):777-81. PubMed ID: 6966049
    [Abstract] [Full Text] [Related]

  • 15. Biochemical aspects of congenital adrenal hyperplasia.
    Honour J.
    J Inherit Metab Dis; 1986 Apr 09; 9 Suppl 1():124-34. PubMed ID: 3097411
    [Abstract] [Full Text] [Related]

  • 16. [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]

  • 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 20; 178():221-228. PubMed ID: 29277706
    [Abstract] [Full Text] [Related]

  • 18. [Problems posed by the association of hemophilia A and congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Boutte P, Madar H, d'Ollone M, Ferracci JP, Bebin B, Lambert JC, Sebag F.
    Pediatrie; 1986 Apr 20; 41(7):559-64. PubMed ID: 3493478
    [Abstract] [Full Text] [Related]

  • 19. [A contribution to the therapy of the congenital adrenal hyperplasia (author's transl)].
    Gleispach H.
    Wien Klin Wochenschr; 1974 Sep 20; 86(17):508-11. PubMed ID: 4408420
    [No Abstract] [Full Text] [Related]

  • 20. [Congenital adrenal hyperplasia as a result of 21-hydroxylase block. Review of 10 cases].
    Belhadj H, Ezzaouia G, Chammakhi S, Bouguerra R, Boukhris R.
    Tunis Med; 1986 Mar 20; 64(3):243-8. PubMed ID: 3490029
    [No Abstract] [Full Text] [Related]

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