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Journal Abstract Search

133 related items for PubMed ID: 15579762

  • 1. 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; 89(12):6087-91. PubMed ID: 15579762
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  • 4. Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosterone.
    Koyama Y, Homma K, Fukami M, Miwa M, Ikeda K, Ogata T, Hasegawa T, Murata M.
    Clin Chem; 2012 Apr; 58(4):741-7. PubMed ID: 22273564
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  • 5. [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
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  • 9. 3 alpha-androstanediol glucuronide in virilizing congenital adrenal hyperplasia: a useful serum metabolic marker of integrated adrenal androgen secretion.
    Pang S, MacGillivray M, Wang M, Jeffries S, Clark A, Rosenthal I, Wiegensberg M, Riddick L.
    J Clin Endocrinol Metab; 1991 Jul 20; 73(1):166-74. PubMed ID: 2045467
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  • 10. 21-Deoxycortisol is a Key Screening Marker for 21-Hydroxylase Deficiency.
    Held PK, Bialk ER, Lasarev MR, Allen DB.
    J Pediatr; 2022 Mar 20; 242():213-219.e1. PubMed ID: 34780778
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  • 11. The balance of cortisol-cortisone interconversion is shifted towards cortisol in neonates with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Kamrath C, Hartmann MF, Wudy SA.
    J Steroid Biochem Mol Biol; 2014 Sep 20; 143():386-91. PubMed ID: 24861266
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  • 12. Profiles of 21-Carbon Steroids in 21-hydroxylase Deficiency.
    Turcu AF, Rege J, Chomic R, Liu J, Nishimoto HK, Else T, Moraitis AG, Palapattu GS, Rainey WE, Auchus RJ.
    J Clin Endocrinol Metab; 2015 Jun 20; 100(6):2283-90. PubMed ID: 25850025
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  • 13. 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 20; 4(1):580-6. PubMed ID: 2552757
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  • 15. Newborn screening for congenital adrenal hyperplasia: additional steroid profile using liquid chromatography-tandem mass spectrometry.
    Janzen N, Peter M, Sander S, Steuerwald U, Terhardt M, Holtkamp U, Sander J.
    J Clin Endocrinol Metab; 2007 Jul 20; 92(7):2581-9. PubMed ID: 17456574
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  • 16. The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency.
    Watanabe K, Tsuji-Hosokawa A, Hashimoto A, Konishi K, Ishige N, Yajima H, Sutani A, Nakatani H, Gau M, Takasawa K, Tajima T, Hasegawa T, Morio T, Kashimada K.
    J Clin Endocrinol Metab; 2022 Nov 25; 107(12):3341-3352. PubMed ID: 36071550
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  • 17. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency.
    Costa-Barbosa FA, Tonetto-Fernandes VF, Carvalho VM, Nakamura OH, Moura V, Bachega TA, Vieira JG, Kater CE.
    Clin Endocrinol (Oxf); 2010 Dec 25; 73(6):700-6. PubMed ID: 20846292
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  • 18. [Congenital adrenal hyperplasia newborn screening: Rio de Janeiro experience].
    Cardoso CB, Fonseca AA, Oliveira Mde F, Pereira BB, Guimarães MM.
    Arq Bras Endocrinol Metabol; 2005 Feb 25; 49(1):112-9. PubMed ID: 16544042
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  • 20. Postnatal changes in blood spot 17-hydroxyprogesterone level in healthy preterm and full-term neonates.
    Sulyok E, Sólyom J, Füller M, Kerekes L.
    Acta Paediatr Hung; 2005 Feb 25; 29(3-4):239-43. PubMed ID: 3269260
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