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150 related items for PubMed ID: 23329749

  • 1. Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche.
    Bizzarri C, Crea F, Marini R, Benevento D, Porzio O, Ravà L, Cappa M.
    J Pediatr Endocrinol Metab; 2012; 25(11-12):1059-64. PubMed ID: 23329749
    [Abstract] [Full Text] [Related]

  • 2. Isolated precocious pubarche: an approach.
    Balducci R, Boscherini B, Mangiantini A, Morellini M, Toscano V.
    J Clin Endocrinol Metab; 1994 Aug; 79(2):582-9. PubMed ID: 8045980
    [Abstract] [Full Text] [Related]

  • 3. Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche.
    Ghizzoni L, Cappa M, Vottero A, Ubertini G, Carta D, Di Iorgi N, Gasco V, Marchesi M, Raggi V, Ibba A, Napoli F, Massimi A, Maghnie M, Loche S, Porzio O.
    Eur J Endocrinol; 2011 Aug; 165(2):307-14. PubMed ID: 21646284
    [Abstract] [Full Text] [Related]

  • 4. Basal levels of 17-hydroxyprogesterone can distinguish children with isolated precocious pubarche.
    Grandone A, Marzuillo P, Luongo C, Toraldo R, Mariani M, Miraglia Del Giudice E, Perrone L.
    Pediatr Res; 2018 Oct; 84(4):533-536. PubMed ID: 29976972
    [Abstract] [Full Text] [Related]

  • 5. Anthropometric and endocrine features in girls with isolated premature pubarche or non-classical congenital adrenal hyperplasia.
    Accetta SG, Di Domênico K, Ritter CG, Ritter AT, Capp E, Spritzer PM.
    J Pediatr Endocrinol Metab; 2004 May; 17(5):767-73. PubMed ID: 15237712
    [Abstract] [Full Text] [Related]

  • 6. Identification of nonclassical 21-hydroxylase deficiency in girls with precocious pubarche.
    Leite MV, Mendonça BB, Arnhold IJ, Estefan V, Nunes C, Nicolau W, Bloise W.
    J Endocrinol Invest; 1991 Jan; 14(1):11-5. PubMed ID: 1646249
    [Abstract] [Full Text] [Related]

  • 7. Adrenal steroidogenic defects in children with precocious pubarche.
    del Balzo P, Borrelli P, Cambiaso P, Danielli E, Cappa M.
    Horm Res; 1992 Jan; 37(4-5):180-4. PubMed ID: 1337057
    [Abstract] [Full Text] [Related]

  • 8. Absence of nonclassical congenital adrenal hyperplasia in patients with precocious adrenarche.
    Morris AH, Reiter EO, Geffner ME, Lippe BM, Itami RM, Mayes DM.
    J Clin Endocrinol Metab; 1989 Oct; 69(4):709-15. PubMed ID: 2550505
    [Abstract] [Full Text] [Related]

  • 9. Precocious pubarche: distinguishing late-onset congenital adrenal hyperplasia from premature adrenarche.
    Armengaud JB, Charkaluk ML, Trivin C, Tardy V, Bréart G, Brauner R, Chalumeau M.
    J Clin Endocrinol Metab; 2009 Aug; 94(8):2835-40. PubMed ID: 19454583
    [Abstract] [Full Text] [Related]

  • 10. Usefulness of an ACTH test in the diagnosis of nonclassical 21-hydroxylase deficiency among children presenting with premature pubarche.
    Ibáñez L, Bonnin MR, Zampolli M, Prat N, Alia PJ, Navarro MA.
    Horm Res; 1995 Aug; 44(2):51-6. PubMed ID: 7590632
    [Abstract] [Full Text] [Related]

  • 11. [Premature pubarche is not always an innocent phenomenon].
    Backes M, Zwaveling-Soonawala N, Kamp GA.
    Ned Tijdschr Geneeskd; 2012 Aug; 156(43):A5147. PubMed ID: 23095481
    [Abstract] [Full Text] [Related]

  • 12. [Late diagnoses of 21-hydroxylase deficiencies in children (after the age of 3 years].
    Carel JC, Marrakchi Z, Roger M, Morel Y, Chaussain JL.
    Ann Pediatr (Paris); 1993 Sep; 40(7):410-20. PubMed ID: 8239392
    [Abstract] [Full Text] [Related]

  • 13. Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?
    Gönç EN, Ozön ZA, Alikaşifoğlu A, Engiz O, Bulum B, Kandemir N.
    Turk J Pediatr; 2011 Sep; 53(3):274-80. PubMed ID: 21980808
    [Abstract] [Full Text] [Related]

  • 14. The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis.
    Ambroziak U, Kępczyńska-Nyk A, Kuryłowicz A, Małunowicz EM, Wójcicka A, Miśkiewicz P, Macech M.
    Clin Endocrinol (Oxf); 2016 Jan; 84(1):23-9. PubMed ID: 26331608
    [Abstract] [Full Text] [Related]

  • 15. Clinical analysis of 78 patients with nonclassical 21-hydroxylase deficiency.
    Liu E, Luo H, Zhou K, Zhang Y.
    Arch Gynecol Obstet; 2023 Sep; 308(3):871-882. PubMed ID: 36773044
    [Abstract] [Full Text] [Related]

  • 16. 17-Hydroxyprogesterone in children, adolescents and adults.
    Honour JW.
    Ann Clin Biochem; 2014 Jul; 51(Pt 4):424-40. PubMed ID: 24711560
    [Abstract] [Full Text] [Related]

  • 17. Results of the ACTH stimulation test in hirsute women.
    Erel CT, Senturk LM, Oral E, Mutlu H, Colgar U, Seyisoglu H, Ertungealp E.
    J Reprod Med; 1999 Mar; 44(3):247-52. PubMed ID: 10202742
    [Abstract] [Full Text] [Related]

  • 18. Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.
    Weintrob N, Brautbar C, Pertzelan A, Josefsberg Z, Dickerman Z, Kauschansky A, Lilos P, Peled D, Phillip M, Israel S.
    Eur J Endocrinol; 2000 Sep; 143(3):397-403. PubMed ID: 11022183
    [Abstract] [Full Text] [Related]

  • 19. Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers.
    Paris F, Tardy V, Chalançon A, Picot MC, Morel Y, Sultan C.
    Gynecol Endocrinol; 2010 May; 26(5):319-24. PubMed ID: 20059433
    [Abstract] [Full Text] [Related]

  • 20. 21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: a multicenter study.
    Moran C, Azziz R, Carmina E, Dewailly D, Fruzzetti F, Ibañez L, Knochenhauer ES, Marcondes JA, Mendonca BB, Pignatelli D, Pugeat M, Rohmer V, Speiser PW, Witchel SF.
    Am J Obstet Gynecol; 2000 Dec; 183(6):1468-74. PubMed ID: 11120512
    [Abstract] [Full Text] [Related]

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