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PUBMED FOR HANDHELDS

Journal Abstract Search


220 related items for PubMed ID: 30530876

  • 1. Assay of steroids by liquid chromatography-tandem mass spectrometry in monitoring 21-hydroxylase deficiency.
    Dahl SR, Nermoen I, Brønstad I, Husebye ES, Løvås K, Thorsby PM.
    Endocr Connect; 2018 Dec; 7(12):1542-1550. PubMed ID: 30530876
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  • 2. Multiplexed steroid profiling of gluco- and mineralocorticoids pathways using a liquid chromatography tandem mass spectrometry method.
    Travers S, Martinerie L, Bouvattier C, Boileau P, Lombès M, Pussard E.
    J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt B):202-211. PubMed ID: 27339652
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  • 3. Serum 21-Deoxycortisol for Diagnosis of Nonclassic Congenital Adrenal Hyperplasia in Women With Androgen Excess.
    Ng JL, Lim EM, Zhang R, Beilby JP, Watts GF, Brown SJ, Stuckey BGA.
    J Clin Endocrinol Metab; 2023 Nov 17; 108(12):e1560-e1570. PubMed ID: 37358001
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  • 4. 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 17; 73(6):700-6. PubMed ID: 20846292
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  • 5. Serum 21-Deoxycortisol, 17-Hydroxyprogesterone, and 11-deoxycortisol in classic congenital adrenal hyperplasia: clinical and hormonal correlations and identification of patients with 11beta-hydroxylase deficiency among a large group with alleged 21-hydroxylase deficiency.
    Tonetto-Fernandes V, Lemos-Marini SH, Kuperman H, Ribeiro-Neto LM, Verreschi IT, Kater CE.
    J Clin Endocrinol Metab; 2006 Jun 17; 91(6):2179-84. PubMed ID: 16551734
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  • 7. Steroid Profiling in the Amniotic Fluid: Reference Range for 12 Steroids and Interest in 21-Hydroxylase Deficiency.
    Pourquet A, Teoli J, Bouty A, Renault L, Roucher F, Mallet D, Rigaud C, Dijoud F, Mouriquand P, Mure PY, Sanlaville D, Ecochard R, Plotton I.
    J Clin Endocrinol Metab; 2023 Apr 13; 108(5):e129-e138. PubMed ID: 36402139
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  • 8. Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) Method for the Quantification of Steroids Androstenedione, Dehydroepiandrosterone, 11-Deoxycortisol, 17-Hydroxyprogesterone, and Testosterone.
    Munar A, Clinton Frazee C, Garg U.
    Methods Mol Biol; 2022 Apr 13; 2546():451-457. PubMed ID: 36127612
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  • 10. Simultaneous quantification of 17α-OH progesterone, 11-deoxycortisol, Δ4-androstenedione, cortisol and cortisone in newborn blood spots using liquid chromatography-tandem mass spectrometry.
    Magnisali P, Chalioti MB, Livadara T, Mataragas M, Paliatsiou S, Malamitsi-Puchner A, Moutsatsou P.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2011 Jun 01; 879(19):1565-72. PubMed ID: 21514253
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  • 11. LC-MS/MS improves screening towards 21-hydroxylase deficiency.
    Ambroziak U, Kępczyńska-Nyk A, Kuryłowicz A, Wysłouch-Cieszyńska A, Małunowicz EM, Bartoszewicz Z, Kondracka A, Jaźwiec R, Pawłowska E, Szcześniak M, Dadlez M, Bednarczuk T.
    Gynecol Endocrinol; 2015 Apr 01; 31(4):296-300. PubMed ID: 25539143
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  • 12. Reassessment of predictive values of ACTH-stimulated serum 21-deoxycortisol and 17-hydroxyprogesterone to identify CYP21A2 heterozygote carriers and nonclassic subjects.
    Costa-Barbosa FA, Carvalho VM, Oliveira KC, Vieira JGH, Kater CE.
    Clin Endocrinol (Oxf); 2021 Oct 01; 95(4):677-685. PubMed ID: 34231242
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  • 14. Steroid profile in dried blood spots by liquid chromatography tandem mass spectrometry: Application to newborn screening for congenital adrenal hyperplasia in China.
    Zhan X, Han L, Qiu W, Gu X, Guo J, Chang S, Wang Y, Zhang H.
    Steroids; 2022 Sep 01; 185():109056. PubMed ID: 35660382
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  • 19. Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: further characterization of classic and non-classic patients and heterozygote carriers.
    Costa-Barbosa FA, Carvalho VM, Nakamura OH, Bachega TA, Vieira JG, Kater CE.
    J Endocrinol Invest; 2011 Sep 01; 34(8):587-92. PubMed ID: 20924223
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  • 20. 21-hydroxylase deficiency transiently mimicking combined 21- and 11beta-hydroxylase deficiency.
    Tonetto-Fernandes V, Lemos-Marini SH, De Mello MP, Ribeiro-Neto LM, Kater CE.
    J Pediatr Endocrinol Metab; 2008 May 01; 21(5):487-94. PubMed ID: 18655532
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