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612 related items for PubMed ID: 31447379

  • 1. Influence of Genotype and Hyperandrogenism on Sexual Function in Women With Congenital Adrenal Hyperplasia.
    Schernthaner-Reiter MH, Baumgartner-Parzer S, Egarter HC, Krebs M, Kautzky-Willer A, Kirchheiner K, Luger A, Bayerle-Eder M.
    J Sex Med; 2019 Oct; 16(10):1529-1540. PubMed ID: 31447379
    [Abstract] [Full Text] [Related]

  • 2. Sexual Function and Depressive Symptoms in Young Women With Nonclassic Congenital Adrenal Hyperplasia.
    Krysiak R, Drosdzol-Cop A, Skrzypulec-Plinta V, Okopien B.
    J Sex Med; 2016 Jan; 13(1):34-9. PubMed ID: 26755084
    [Abstract] [Full Text] [Related]

  • 3. Sexual orientation in women with classical or non-classical congenital adrenal hyperplasia as a function of degree of prenatal androgen excess.
    Meyer-Bahlburg HF, Dolezal C, Baker SW, New MI.
    Arch Sex Behav; 2008 Feb; 37(1):85-99. PubMed ID: 18157628
    [Abstract] [Full Text] [Related]

  • 4. Clinical and hormonal characteristics in heterozygote carriers of congenital adrenal hyperplasia.
    Guarnotta V, Niceta M, Bono M, Marchese S, Fabiano C, Indelicato S, Di Gaudio F, Garofalo P, Giordano C.
    J Steroid Biochem Mol Biol; 2020 Apr; 198():105554. PubMed ID: 31805392
    [Abstract] [Full Text] [Related]

  • 5. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Coeli-Lacchini FB, Turatti W, Elias PC, Elias LL, Martinelli CE, Moreira AC, Antonini SR, de Castro M.
    Gene; 2013 Sep 10; 526(2):239-45. PubMed ID: 23570880
    [Abstract] [Full Text] [Related]

  • 6. Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort.
    Krone N, Rose IT, Willis DS, Hodson J, Wild SH, Doherty EJ, Hahner S, Parajes S, Stimson RH, Han TS, Carroll PV, Conway GS, Walker BR, MacDonald F, Ross RJ, Arlt W, United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE).
    J Clin Endocrinol Metab; 2013 Feb 10; 98(2):E346-54. PubMed ID: 23337727
    [Abstract] [Full Text] [Related]

  • 7.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, Nimkarn S, Gangishetti PK, Yau M, New MI.
    ; 1993 Feb 10. PubMed ID: 20301350
    [Abstract] [Full Text] [Related]

  • 8. [Diffuse hypertrichosis revealing non-classical congenital adrenal hyperplasia].
    Berthin C, Sibilia P, Martins-Hericher J, Donzeau A, Martin L.
    Ann Dermatol Venereol; 2018 Apr 10; 145(4):270-277. PubMed ID: 29525066
    [Abstract] [Full Text] [Related]

  • 9. Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Saho R, Dolzan V, Zerjav Tansek M, Pastorakova A, Petrovic R, Knapkova M, Trebusak Podkrajsek K, Suput Omladic J, Bertok S, Avbelj Stefanija M, Kotnik P, Battelino T, Pribilincova Z, Groselj U.
    Front Endocrinol (Lausanne); 2023 Apr 10; 14():1134133. PubMed ID: 37008950
    [Abstract] [Full Text] [Related]

  • 10. Sexual function in women with androgen excess disorders: classic forms of congenital adrenal hyperplasia and polycystic ovary syndrome.
    Kępczyńska-Nyk A, Kuryłowicz A, Nowak A, Bednarczuk T, Ambroziak U.
    J Endocrinol Invest; 2021 Mar 10; 44(3):505-513. PubMed ID: 32557272
    [Abstract] [Full Text] [Related]

  • 11. Sexual function and surgical outcome in women with congenital adrenal hyperplasia due to CYP21A2 deficiency: clinical perspective and the patients' perception.
    Nordenström A, Frisén L, Falhammar H, Filipsson H, Holmdahl G, Janson PO, Thorén M, Hagenfeldt K, Nordenskjöld A.
    J Clin Endocrinol Metab; 2010 Aug 10; 95(8):3633-40. PubMed ID: 20466782
    [Abstract] [Full Text] [Related]

  • 12. A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance.
    Khattab A, Yuen T, Al-Malki S, Yau M, Kazmi D, Sun L, Harbison M, Haider S, Zaidi M, New MI.
    Ann N Y Acad Sci; 2016 Jan 10; 1364(1):5-10. PubMed ID: 26291314
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  • 13. Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women.
    Blanché H, Vexiau P, Clauin S, Le Gall I, Fiet J, Mornet E, Dausset J, Bellanné-Chantelot C.
    Hum Genet; 1997 Nov 10; 101(1):56-60. PubMed ID: 9385370
    [Abstract] [Full Text] [Related]

  • 14. CYP21A2 Gene Pathogenic Variants: A Multicenter Study on Genotype-Phenotype Correlation from a Portuguese Pediatric Cohort.
    Santos-Silva R, Cardoso R, Lopes L, Fonseca M, Espada F, Sampaio L, Brandão C, Antunes A, Bragança G, Coelho R, Bernardo T, Vieira P, Morais R, Leite AL, Ribeiro L, Carvalho B, Grangeia A, Oliveira R, Oliveira MJ, Rey V, Rosmaninho-Salgado J, Marques B, Garcia AM, Meireles A, Carvalho J, Sequeira A, Mirante A, Borges T, on behalf of the Portuguese Society of Pediatric Endocrinology and Diabetology.
    Horm Res Paediatr; 2019 Nov 10; 91(1):33-45. PubMed ID: 30889569
    [Abstract] [Full Text] [Related]

  • 15. Characteristics of In2G Variant in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
    Kocova M, Concolino P, Falhammar H.
    Front Endocrinol (Lausanne); 2021 Nov 10; 12():788812. PubMed ID: 35140681
    [Abstract] [Full Text] [Related]

  • 16. Congenital adrenal hyperplasia and risk for psychiatric disorders in girls and women born between 1915 and 2010: A total population study.
    Engberg H, Butwicka A, Nordenström A, Hirschberg AL, Falhammar H, Lichtenstein P, Nordenskjöld A, Frisén L, Landén M.
    Psychoneuroendocrinology; 2015 Oct 10; 60():195-205. PubMed ID: 26184920
    [Abstract] [Full Text] [Related]

  • 17. Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
    Concolino P, Perrucci A, Carrozza C, Urbani A.
    Mol Diagn Ther; 2023 Sep 10; 27(5):621-630. PubMed ID: 37548905
    [Abstract] [Full Text] [Related]

  • 18. Characterization of the CYP21A2 Gene Mutations in Children with Classic Congenital Adrenal Hyperplasia.
    Saraf S, Srivastava P, Panigrahi I, Seenappa V, Kumar R, Yadav J, Daniel R, Dayal D.
    Indian J Pediatr; 2024 Feb 10; 91(2):137-142. PubMed ID: 35094236
    [Abstract] [Full Text] [Related]

  • 19. Steroid 21-hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype-phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia.
    Marino R, Ramirez P, Galeano J, Perez Garrido N, Rocco C, Ciaccio M, Warman DM, Guercio G, Chaler E, Maceiras M, Bergadá I, Gryngarten M, Balbi V, Pardes E, Rivarola MA, Belgorosky A.
    Clin Endocrinol (Oxf); 2011 Oct 10; 75(4):427-35. PubMed ID: 21609351
    [Abstract] [Full Text] [Related]

  • 20. CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia.
    Moura-Massari VO, Bugano DD, Marcondes JA, Gomes LG, Mendonca BB, Bachega TA.
    Horm Metab Res; 2013 Apr 10; 45(4):301-7. PubMed ID: 23322511
    [Abstract] [Full Text] [Related]


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