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Journal Abstract Search

611 related items for PubMed ID: 31447379

  • 21. Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report.
    Sumińska M, Bogusz-Górna K, Wegner D, Fichna M.
    Int J Mol Sci; 2020 Jun 29; 21(13):. PubMed ID: 32610579
    [Abstract] [Full Text] [Related]

  • 22. Hyperinsulinemia and insulin insensitivity in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the relationship between serum leptin levels and chronic hyperinsulinemia.
    Saygili F, Oge A, Yilmaz C.
    Horm Res; 2005 Jun 29; 63(6):270-4. PubMed ID: 15956788
    [Abstract] [Full Text] [Related]

  • 23. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor.
    Aycan Z, Keskin M, Lafcı NG, Savaş-Erdeve Ş, Baş F, Poyrazoğlu Ş, Öztürk P, Parlak M, Ercan O, Güran T, Hatipoğlu N, Uçaktürk SA, Çatlı G, Akyürek N, Önder A, Kılınç S, Çetinkaya S.
    Eur J Med Genet; 2022 Dec 29; 65(12):104654. PubMed ID: 36343887
    [Abstract] [Full Text] [Related]

  • 24. [Health status of adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Bachelot A, Touraine P.
    Presse Med; 2014 Apr 29; 43(4 Pt 1):428-37. PubMed ID: 24630263
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  • 25. Comprehensive genetic analysis of 182 unrelated families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Finkielstain GP, Chen W, Mehta SP, Fujimura FK, Hanna RM, Van Ryzin C, McDonnell NB, Merke DP.
    J Clin Endocrinol Metab; 2011 Jan 29; 96(1):E161-72. PubMed ID: 20926536
    [Abstract] [Full Text] [Related]

  • 26. The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene.
    Livadas S, Dracopoulou M, Dastamani A, Sertedaki A, Maniati-Christidi M, Magiakou AM, Kanaka-Gantenbein C, Chrousos GP, Dacou-Voutetakis C.
    Clin Endocrinol (Oxf); 2015 Apr 29; 82(4):543-9. PubMed ID: 25041270
    [Abstract] [Full Text] [Related]

  • 27. Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene.
    Fanis P, Skordis N, Phylactou LA, Neocleous V.
    Hormones (Athens); 2023 Mar 29; 22(1):71-77. PubMed ID: 36264454
    [Abstract] [Full Text] [Related]

  • 28. Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency.
    New MI, Abraham M, Gonzalez B, Dumic M, Razzaghy-Azar M, Chitayat D, Sun L, Zaidi M, Wilson RC, Yuen T.
    Proc Natl Acad Sci U S A; 2013 Feb 12; 110(7):2611-6. PubMed ID: 23359698
    [Abstract] [Full Text] [Related]

  • 29. Non-classical congenital adrenal hyperplasia.
    Dacou-Voutetakis C, Dracopoulou M.
    Pediatr Endocrinol Rev; 2006 Jan 12; 3 Suppl 1():195-7. PubMed ID: 16641859
    [Abstract] [Full Text] [Related]

  • 30. Congenital adrenal hyperplasia.
    Pang S.
    Baillieres Clin Obstet Gynaecol; 1997 Jun 12; 11(2):281-306. PubMed ID: 9536212
    [Abstract] [Full Text] [Related]

  • 31. Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia.
    Torres N, Mello MP, Germano CM, Elias LL, Moreira AC, Castro M.
    Braz J Med Biol Res; 2003 Oct 12; 36(10):1311-8. PubMed ID: 14502362
    [Abstract] [Full Text] [Related]

  • 32. Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Golmard JL, Tardy V, Morel Y, Clauin S, Coussieu C, Boudou P, Mowzowicz I, Bachelot A, Touraine P, Kuttenn F.
    J Clin Endocrinol Metab; 2010 Mar 12; 95(3):1182-90. PubMed ID: 20080854
    [Abstract] [Full Text] [Related]

  • 33. Gender role behavior, sexuality, and psychosocial adaptation in women with congenital adrenal hyperplasia due to CYP21A2 deficiency.
    Frisén L, Nordenström A, Falhammar H, Filipsson H, Holmdahl G, Janson PO, Thorén M, Hagenfeldt K, Möller A, Nordenskjöld A.
    J Clin Endocrinol Metab; 2009 Sep 12; 94(9):3432-9. PubMed ID: 19567521
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  • 34. Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.
    Dubey S, Tardy V, Chowdhury MR, Gupta N, Jain V, Deka D, Sharma P, Morel Y, Kabra M.
    Indian J Med Res; 2017 Feb 12; 145(2):194-202. PubMed ID: 28639595
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  • 35. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Feb 12; 52(11-12):447-54. PubMed ID: 10748766
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  • 36. Congenital adrenal hyperplasia because of 21-hydroxylase deficiency. A genetic disorder of interest to obstetricians and gynecologists.
    Trakakis E, Loghis C, Kassanos D.
    Obstet Gynecol Surv; 2009 Mar 12; 64(3):177-89. PubMed ID: 19228439
    [Abstract] [Full Text] [Related]

  • 37. Differences in hormonal levels between heterozygous CYP21A2 pathogenic variant carriers, non-carriers, and females with non-classic congenital hyperplasia.
    Silva RS, Carvalho B, Pedro J, Castro-Correia C, Carvalho D, Carvalho F, Fontoura M.
    Arch Endocrinol Metab; 2022 Apr 28; 66(2):168-175. PubMed ID: 35289513
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  • 38. Fertility in patients with congenital adrenal hyperplasia.
    Reichman DE, White PC, New MI, Rosenwaks Z.
    Fertil Steril; 2014 Feb 28; 101(2):301-9. PubMed ID: 24355046
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  • 39. Targeted gene panel sequencing for molecular diagnosis of congenital adrenal hyperplasia.
    Wang W, Han R, Yang Z, Zheng S, Li H, Wan Z, Qi Y, Sun S, Ye L, Ning G.
    J Steroid Biochem Mol Biol; 2021 Jul 28; 211():105899. PubMed ID: 33864926
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  • 40. Genotype-phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21-hydroxylase deficiency.
    Xu C, Jia W, Cheng X, Ying H, Chen J, Xu J, Guan Q, Zhou X, Zheng D, Li G, Zhao J.
    Mol Genet Genomic Med; 2019 Jun 28; 7(6):e671. PubMed ID: 30968594
    [Abstract] [Full Text] [Related]

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