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Journal Abstract Search


290 related items for PubMed ID: 16895568

  • 1. [Acne infantum as presenting symptom of congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency].
    Harde V, Müller M, Sippell WG, Schwarz T, Fölster-Holst R.
    J Dtsch Dermatol Ges; 2006 Aug; 4(8):654-7. PubMed ID: 16895568
    [Abstract] [Full Text] [Related]

  • 2. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency.
    Peter M.
    Semin Reprod Med; 2002 Aug; 20(3):249-54. PubMed ID: 12428205
    [Abstract] [Full Text] [Related]

  • 3. Steroid responsive hypertension secondary to 11-beta hydroxylase deficiency--a case report.
    Isiavwe AR, Ekpebegh CO, Fasanmade OA, Ohwovoriole AE.
    West Afr J Med; 2008 Jul; 27(3):182-5. PubMed ID: 19256327
    [Abstract] [Full Text] [Related]

  • 4. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Trends Endocrinol Metab; 2008 Apr; 19(3):96-9. PubMed ID: 18294861
    [Abstract] [Full Text] [Related]

  • 5. [Congenital adrenal hyperplasia: clinical aspects and neonatal screening].
    Stikkelbroeck MM, Otten BJ.
    Ned Tijdschr Geneeskd; 2002 Feb 09; 146(6):246-9. PubMed ID: 11865652
    [Abstract] [Full Text] [Related]

  • 6. Congenital adrenal hyperplasia and multiple sclerosis: is there an increased risk of multiple sclerosis in individuals with congenital adrenal hyperplasia?
    Bergamaschi R, Livieri C, Candeloro E, Uggetti C, Franciotta D, Cosi V.
    Arch Neurol; 2004 Dec 09; 61(12):1953-5. PubMed ID: 15596619
    [Abstract] [Full Text] [Related]

  • 7. [Prenatal diagnosis and treatment of adrenogenital syndrome. Prevent virilization of female fetuses].
    Lajic S, Bui TH, Holst M, Ritzén M, Wedell A.
    Lakartidningen; 1997 Dec 10; 94(50):4781-6. PubMed ID: 9445959
    [Abstract] [Full Text] [Related]

  • 8. Steroid 11 beta-hydroxylase deficiency and related disorders.
    White PC, Speiser PW.
    Endocrinol Metab Clin North Am; 1994 Jun 10; 23(2):325-39. PubMed ID: 8070425
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis and treatment of congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Pediatr Endocrinol Rev; 1994 Jun 10; 4(2):99-105. PubMed ID: 17342026
    [Abstract] [Full Text] [Related]

  • 10. Long-term consequences of childhood-onset congenital adrenal hyperplasia.
    White PC, Speiser PW.
    Best Pract Res Clin Endocrinol Metab; 2002 Jun 10; 16(2):273-88. PubMed ID: 12064893
    [Abstract] [Full Text] [Related]

  • 11. Novel missense mutations, GCC [Ala306]- > GTC [Val] and ACG [Thr318]- > CCG [Pro], in the CYP11B1 gene cause steroid 11beta-hydroxylase deficiency in the Chinese.
    Lee HH, Won GS, Chao HT, Lee YJ, Chung BC.
    Clin Endocrinol (Oxf); 2005 Apr 10; 62(4):418-22. PubMed ID: 15807871
    [Abstract] [Full Text] [Related]

  • 12. Congenital adrenal hyperplasia.
    Demirci C, Witchel SF.
    Dermatol Ther; 2008 Apr 10; 21(5):340-53. PubMed ID: 18844712
    [Abstract] [Full Text] [Related]

  • 13. Neonatal salt-wasting and 11 beta-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11 beta-hydroxylase).
    Ezquieta B, Luzuriaga C.
    Clin Genet; 2004 Sep 10; 66(3):229-35. PubMed ID: 15324322
    [Abstract] [Full Text] [Related]

  • 14. Acne and non-classic congenital adrenal hyperplasia.
    Falhammar H.
    N Z Med J; 2008 Jun 06; 121(1275):94-5. PubMed ID: 18551162
    [No Abstract] [Full Text] [Related]

  • 15. Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiency.
    Krone N, Grischuk Y, Müller M, Volk RE, Grötzinger J, Holterhus PM, Sippell WG, Riepe FG.
    J Clin Endocrinol Metab; 2006 Jul 06; 91(7):2682-8. PubMed ID: 16670167
    [Abstract] [Full Text] [Related]

  • 16. Congenital adrenal hyperplasia with 11 beta-hydroxylase deficiency.
    Chang SH, Lee HH, Wang PJ, Chen JH, Chu SY.
    J Formos Med Assoc; 2004 Nov 06; 103(11):860-4. PubMed ID: 15549155
    [Abstract] [Full Text] [Related]

  • 17. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Nov 06; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 18. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, Lin-Su K, New MI.
    Endocrinol Metab Clin North Am; 2009 Dec 06; 38(4):699-718. PubMed ID: 19944288
    [Abstract] [Full Text] [Related]

  • 19. A case of 11beta-hydroxylase deficiency detected in a newborn screening program by second-tier LC-MS/MS.
    Peter M, Janzen N, Sander S, Korsch E, Riepe FG, Sander J.
    Horm Res; 2008 Dec 06; 69(4):253-6. PubMed ID: 18204274
    [Abstract] [Full Text] [Related]

  • 20. [A case of bilateral testicular tumors with congenital adrenal hyperplasia].
    Tsurukawa H, Iuchi H, Tokumitsu M, Yamaguchi S, Hashimoto H, Yachiku S.
    Hinyokika Kiyo; 2000 May 06; 46(5):311-3. PubMed ID: 10876752
    [Abstract] [Full Text] [Related]


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