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139 related items for PubMed ID: 23329749

  • 21. Establishment of Clinical and Lab Algorithms for the Identification of Carriers of Mutations in CYP21A2 - A Study of 365 Children and Adolescents.
    Meinel J, Haverkamp T, Wünsche F, Richter-Unruh A.
    Exp Clin Endocrinol Diabetes; 2021 Jul; 129(7):492-499. PubMed ID: 32838438
    [Abstract] [Full Text] [Related]

  • 22. Precocious puberty in children.
    Atta I, Laghari TM, Khan YN, Lone SW, Ibrahim M, Raza J.
    J Coll Physicians Surg Pak; 2015 Feb; 25(2):124-8. PubMed ID: 25703757
    [Abstract] [Full Text] [Related]

  • 23. Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels.
    Sakkal-Alkaddour H, Zhang L, Yang X, Chang YT, Kappy M, Slover RS, Jorgensen V, Pang S.
    J Clin Endocrinol Metab; 1996 Nov; 81(11):3961-5. PubMed ID: 8923844
    [Abstract] [Full Text] [Related]

  • 24. Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations.
    Bachega TA, Brenlha EM, Billerbeck AE, Marcondes JA, Madureira G, Arnhold IJ, Mendonca BB.
    J Clin Endocrinol Metab; 2002 Feb; 87(2):786-90. PubMed ID: 11836321
    [Abstract] [Full Text] [Related]

  • 25. Basal 17-hydroxyprogesterone cannot accurately predict nonclassical congenital adrenal hyperplasia in children and adolescents.
    Bello R, Lebenthal Y, Lazar L, Shalitin S, Tenenbaum A, Phillip M, de Vries L.
    Acta Paediatr; 2017 Jan; 106(1):155-160. PubMed ID: 27743484
    [Abstract] [Full Text] [Related]

  • 26. Exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation and evidence for CYP21B gene point mutations in true precocious puberty.
    Cisternino M, Dondi E, Martinetti M, Lorini R, Salvaneschi L, Cuccia M, Severi F.
    Clin Endocrinol (Oxf); 1998 May; 48(5):555-60. PubMed ID: 9666866
    [Abstract] [Full Text] [Related]

  • 27. Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome.
    Onder A, Aycan Z, Cetinkaya S, Kendirci HN, Bas VN, Agladioglu SY.
    J Pediatr Endocrinol Metab; 2012 May; 25(7-8):681-5. PubMed ID: 23155693
    [Abstract] [Full Text] [Related]

  • 28. Clinical presentation of children with premature adrenarche.
    von Oettingen J, Sola Pou J, Levitsky LL, Misra M.
    Clin Pediatr (Phila); 2012 Dec; 51(12):1140-9. PubMed ID: 22893187
    [Abstract] [Full Text] [Related]

  • 29. Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
    Mermejo LM, Elias LL, Marui S, Moreira AC, Mendonca BB, de Castro M.
    J Clin Endocrinol Metab; 2005 Mar; 90(3):1287-93. PubMed ID: 15585552
    [Abstract] [Full Text] [Related]

  • 30. [Pubic hair in children and late onset congenital adrenal hyperplasia].
    Mota A, Fonseca G, Rebelo I, Crespo ME.
    Acta Med Port; 1991 Mar; 4(4):188-90. PubMed ID: 1767710
    [Abstract] [Full Text] [Related]

  • 31. Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Bachega TA, Billerbeck AE, Marcondes JA, Madureira G, Arnhold IJ, Mendonca BB.
    Clin Endocrinol (Oxf); 2000 May; 52(5):601-7. PubMed ID: 10792340
    [Abstract] [Full Text] [Related]

  • 32. Genetic defects of steroidogenesis in premature pubarche.
    Temeck JW, Pang SY, Nelson C, New MI.
    J Clin Endocrinol Metab; 1987 Mar; 64(3):609-17. PubMed ID: 3029158
    [Abstract] [Full Text] [Related]

  • 33. Extensive clinical experience: nonclassical 21-hydroxylase deficiency.
    New MI.
    J Clin Endocrinol Metab; 2006 Nov; 91(11):4205-14. PubMed ID: 16912124
    [Abstract] [Full Text] [Related]

  • 34. A proof of concept of a machine learning algorithm to predict late-onset 21-hydroxylase deficiency in children with premature pubic hair.
    Agnani H, Bachelot G, Eguether T, Ribault B, Fiet J, Le Bouc Y, Netchine I, Houang M, Lamazière A.
    J Steroid Biochem Mol Biol; 2022 Jun; 220():106085. PubMed ID: 35292353
    [Abstract] [Full Text] [Related]

  • 35. Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia.
    Silveira EL, Elnecave RH, dos Santos EP, Moura V, Pinto EM, van der Linden Nader I, Mendonca BB, Bachega TA.
    Clin Genet; 2009 Dec; 76(6):503-10. PubMed ID: 19930153
    [Abstract] [Full Text] [Related]

  • 36. Congenital adrenal hyperplasia in the Bahamas due to 21-hydroxylase deficiency.
    Peter S, McDigean G, Sandiford P, Smith T.
    West Indian Med J; 2006 Mar; 55(2):110-2. PubMed ID: 16921705
    [Abstract] [Full Text] [Related]

  • 37. Non-classical 21-hydroxylase deficiency in children: association of adrenocorticotropic hormone-stimulated 17-hydroxyprogesterone with the risk of compound heterozygosity with severe mutations.
    Ezquieta B, Cueva E, Varela J, Oliver A, Fernández J, Jariego C.
    Acta Paediatr; 2002 Mar; 91(8):892-8. PubMed ID: 12222711
    [Abstract] [Full Text] [Related]

  • 38. Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening.
    Sarafoglou K, Lorentz CP, Otten N, Oetting WS, Grebe SK.
    Clin Genet; 2012 Jul; 82(1):64-70. PubMed ID: 21534945
    [Abstract] [Full Text] [Related]

  • 39. Premature Pubarche: Time to Revise the Diagnostic Approach?
    Baronio F, Marzatico A, De Iasio R, Ortolano R, Fanolla A, Radetti G, Balsamo A, Pession A, Cassio A.
    J Clin Med; 2023 Mar 11; 12(6):. PubMed ID: 36983190
    [Abstract] [Full Text] [Related]

  • 40. [Causes of precocious puberty in children referred for evaluation in hospital conditions].
    Januszek-Trzciakowska A, Kalina-Faska B, Kalina M, Zachurzok-Buczyńska A, Gawlik A, Małecka-Tendera E.
    Endokrynol Pol; 2007 Mar 11; 58(4):291-6. PubMed ID: 18058720
    [Abstract] [Full Text] [Related]

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