These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

189 related items for PubMed ID: 9385370

  • 1. 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; 101(1):56-60. PubMed ID: 9385370
    [Abstract] [Full Text] [Related]

  • 2. The frequency of CYP 21 gene mutations in Turkish women with hyperandrogenism.
    Kelestimur F, Everest H, Dundar M, Tanriverdi F, White C, Witchel SF.
    Exp Clin Endocrinol Diabetes; 2009 May; 117(5):205-8. PubMed ID: 19085698
    [Abstract] [Full Text] [Related]

  • 3. The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations.
    Escobar-Morreale HF, San Millán JL, Smith RR, Sancho J, Witchel SF.
    Fertil Steril; 1999 Oct; 72(4):629-38. PubMed ID: 10521100
    [Abstract] [Full Text] [Related]

  • 4. How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency.
    L'Allemand D, Tardy V, Grüters A, Schnabel D, Krude H, Morel Y.
    J Clin Endocrinol Metab; 2000 Dec; 85(12):4562-7. PubMed ID: 11134109
    [Abstract] [Full Text] [Related]

  • 5. Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acne.
    Ostlere LS, Rumsby G, Holownia P, Jacobs HS, Rustin MH, Honour JW.
    Clin Endocrinol (Oxf); 1998 Feb; 48(2):209-15. PubMed ID: 9579234
    [Abstract] [Full Text] [Related]

  • 6. Hyperandrogenism in carriers of CYP21 mutations: the role of genotype.
    Admoni O, Israel S, Lavi I, Gur M, Tenenbaum-Rakover Y.
    Clin Endocrinol (Oxf); 2006 Jun; 64(6):645-51. PubMed ID: 16712666
    [Abstract] [Full Text] [Related]

  • 7. Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status.
    Dolzan V, Prezelj J, Vidan-Jeras B, Breskvar K.
    Eur J Endocrinol; 1999 Aug; 141(2):132-9. PubMed ID: 10427156
    [Abstract] [Full Text] [Related]

  • 8. Nonclassic 21-hydroxylase deficiency in Croatia.
    Dumic M, Ille J, Zunec R, Plavsic V, Francetic I, Skrabic V, Janjanin N, Spehar A, Wei J, Wilson RC, New MI.
    J Pediatr Endocrinol Metab; 2004 Feb; 17(2):157-64. PubMed ID: 15055349
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. A prospective study of the prevalence of nonclassical congenital adrenal hyperplasia among women presenting with hyperandrogenic symptoms and signs.
    Escobar-Morreale HF, Sanchón R, San Millán JL.
    J Clin Endocrinol Metab; 2008 Feb 10; 93(2):527-33. PubMed ID: 18000084
    [Abstract] [Full Text] [Related]

  • 11. Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.
    Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Tardy V, Billaud L, Laborde K, Coussieu C, Morel Y, Vaury C, Golmard JL, Claustre A, Mornet E, Chakhtoura Z, Mowszowicz I, Bachelot A, Touraine P, Kuttenn F.
    J Clin Endocrinol Metab; 2009 May 10; 94(5):1570-8. PubMed ID: 19208730
    [Abstract] [Full Text] [Related]

  • 12. Molecular abnormalities of the 21-hydroxylase gene in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation.
    Azziz R, Owerbach D.
    Am J Obstet Gynecol; 1995 Mar 10; 172(3):914-8. PubMed ID: 7892885
    [Abstract] [Full Text] [Related]

  • 13. 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 10; 16(10):1529-1540. PubMed ID: 31447379
    [Abstract] [Full Text] [Related]

  • 14. Hormonal evaluation and mutation screening for steroid 21-hydroxylase deficiency in patients with unilateral and bilateral adrenal incidentalomas.
    Patócs A, Tóth M, Barta C, Sasvári-Székely M, Varga I, Szücs N, Jakab C, Gláz E, Rácz K.
    Eur J Endocrinol; 2002 Sep 10; 147(3):349-55. PubMed ID: 12213672
    [Abstract] [Full Text] [Related]

  • 15. 17-Hydroxyprogesterone in children, adolescents and adults.
    Honour JW.
    Ann Clin Biochem; 2014 Jul 10; 51(Pt 4):424-40. PubMed ID: 24711560
    [Abstract] [Full Text] [Related]

  • 16. Hyperandrogenism and manifesting heterozygotes for 21-hydroxylase deficiency.
    Witchel SF, Lee PA, Suda-Hartman M, Hoffman EP.
    Biochem Mol Med; 1997 Dec 10; 62(2):151-8. PubMed ID: 9441866
    [Abstract] [Full Text] [Related]

  • 17. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.
    Speiser PW, New MI.
    J Clin Endocrinol Metab; 1987 Jan 10; 64(1):86-91. PubMed ID: 3023431
    [Abstract] [Full Text] [Related]

  • 18. Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients.
    Dain LB, Buzzalino ND, Oneto A, Belli S, Stivel M, Pasqualini T, Minutolo C, Charreau EH, Alba LG.
    Clin Endocrinol (Oxf); 2002 Feb 10; 56(2):239-45. PubMed ID: 11874416
    [Abstract] [Full Text] [Related]

  • 19. Molecular basis of nonclassical steroid 21-hydroxylase deficiency detected by neonatal mass screening in Japan.
    Tajima T, Fujieda K, Nakae J, Toyoura T, Shimozawa K, Kusuda S, Goji K, Nagashima T, Cutler GB.
    J Clin Endocrinol Metab; 1997 Jul 10; 82(7):2350-6. PubMed ID: 9215318
    [Abstract] [Full Text] [Related]

  • 20. Variants of the type II 3beta-hydroxysteroid dehydrogenase gene in children with premature pubic hair and hyperandrogenic adolescents.
    Nayak S, Lee PA, Witchel SF.
    Mol Genet Metab; 1998 Jul 10; 64(3):184-92. PubMed ID: 9719627
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.