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Journal Abstract Search

148 related items for PubMed ID: 3097411

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

  • 2. 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; 165(Pt B):396-406. PubMed ID: 27544322
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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 Oct; 16(1-2):57-75. PubMed ID: 6278806
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. The diagnosis of congenital adrenal hyperplasia in the newborn by gas chromatography/mass spectrometry analysis of random urine specimens.
    Caulfield MP, Lynn T, Gottschalk ME, Jones KL, Taylor NF, Malunowicz EM, Shackleton CH, Reitz RE, Fisher DA.
    J Clin Endocrinol Metab; 2002 Aug; 87(8):3682-90. PubMed ID: 12161496
    [Abstract] [Full Text] [Related]

  • 7. Urinary steroidomic profiles by LC-MS/MS to monitor classic 21-Hydroxylase deficiency.
    Pussard E, Travers S, Bouvattier C, Xue QY, Cosson C, Viengchareun S, Martinerie L, Lombès M.
    J Steroid Biochem Mol Biol; 2020 Apr; 198():105553. PubMed ID: 31778802
    [Abstract] [Full Text] [Related]

  • 8. 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; 178():221-228. PubMed ID: 29277706
    [Abstract] [Full Text] [Related]

  • 9. Neonatal screening for congenital adrenal hyperplasia in Southern Brazil: a population based study with 108,409 infants.
    Kopacek C, de Castro SM, Prado MJ, da Silva CM, Beltrão LA, Spritzer PM.
    BMC Pediatr; 2017 Jan 17; 17(1):22. PubMed ID: 28095810
    [Abstract] [Full Text] [Related]

  • 10. Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants.
    Nordenström A, Wedell A, Hagenfeldt L, Marcus C, Larsson A.
    Pediatrics; 2001 Oct 17; 108(4):E68. PubMed ID: 11581476
    [Abstract] [Full Text] [Related]

  • 11. Congenital adrenal hyperplasia: clinical symptoms and diagnostic methods.
    Podgórski R, Aebisher D, Stompor M, Podgórska D, Mazur A.
    Acta Biochim Pol; 2018 Oct 17; 65(1):25-33. PubMed ID: 29543924
    [Abstract] [Full Text] [Related]

  • 12. Correlation of blood-spot 17-hydroxyprogesterone daily profiles and urinary steroid profiles in congenital adrenal hyperplasia.
    Erhardt E, Sólyom J, Homoki J, Juricskay S, Soltész G.
    J Pediatr Endocrinol Metab; 2000 Feb 17; 13(2):205-10. PubMed ID: 10711668
    [Abstract] [Full Text] [Related]

  • 13. Effect of single and multiple courses of prenatal corticosteroids on 17-hydroxyprogesterone levels: implication for neonatal screening of congenital adrenal hyperplasia.
    Gatelais F, Berthelot J, Beringue F, Descamps P, Bonneau D, Limal JM, Coutant R.
    Pediatr Res; 2004 Nov 17; 56(5):701-5. PubMed ID: 15371568
    [Abstract] [Full Text] [Related]

  • 14. Definitive diagnosis of enzymatic deficiencies of steroidogenesis in at-risk newborns and infants by urinary marker analysis using GC/MS-SIM.
    Małunowicz EM, Mitkowska Z, Bal K, Nizankowska-Błaz T, Moszczyńska E, Iwanicka Z, Romer TE.
    Horm Res; 1997 Nov 17; 48(6):243-51. PubMed ID: 9402240
    [Abstract] [Full Text] [Related]

  • 15. Diagnosis of 21-hydroxylase deficiency by urinary metabolite ratios using gas chromatography-mass spectrometry analysis: Reference values for neonates and infants.
    Kamrath C, Hartmann MF, Boettcher C, Zimmer KP, Wudy SA.
    J Steroid Biochem Mol Biol; 2016 Feb 17; 156():10-6. PubMed ID: 26493852
    [Abstract] [Full Text] [Related]

  • 16. Steroid profiling for congenital adrenal hyperplasia by tandem mass spectrometry as a second-tier test reduces follow-up burdens in a tertiary care hospital: a retrospective and prospective evaluation.
    Seo JY, Park HD, Kim JW, Oh HJ, Yang JS, Chang YS, Park WS, Lee SY.
    J Perinat Med; 2014 Jan 17; 42(1):121-7. PubMed ID: 23989111
    [Abstract] [Full Text] [Related]

  • 17. Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography-tandem mass spectrometry.
    Janzen N, Sander S, Terhardt M, Steuerwald U, Peter M, Das AM, Sander J.
    Steroids; 2011 Dec 11; 76(13):1437-42. PubMed ID: 21839763
    [Abstract] [Full Text] [Related]

  • 18. 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 Dec 11; 38(1):65-78. PubMed ID: 3428234
    [No Abstract] [Full Text] [Related]

  • 19. Dried Blood Spot Multiplexed Steroid Profiling Using Liquid Chromatography Tandem Mass Spectrometry in Korean Neonates.
    Choi R, Park HD, Oh HJ, Lee K, Song J, Lee SY.
    Ann Lab Med; 2019 May 11; 39(3):263-270. PubMed ID: 30623618
    [Abstract] [Full Text] [Related]

  • 20. Cortisol in dried blood screening specimens from newborns with raised 17-hydroxyprogesterone and congenital adrenal hyperplasia.
    Mitchell ML, Hermos RJ.
    Clin Endocrinol (Oxf); 1998 Jun 11; 48(6):757-60. PubMed ID: 9713565
    [Abstract] [Full Text] [Related]

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