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Journal Abstract Search

103 related items for PubMed ID: 22815032

  • 1. Congenital adrenal hyperplasia masquerading as periodic paralysis in an adolescent girl.
    Sathya A, Ganesan R, Kumar A.
    Singapore Med J; 2012 Jul; 53(7):e148-9. PubMed ID: 22815032
    [Abstract] [Full Text] [Related]

  • 2. 17-Hydroxyprogesterone deficiency as a cause of sexual infantilism and arterial hypertension: laboratory and molecular diagnosis--a case report.
    Benetti-Pinto CL, Vale D, Garmes H, Bedone A.
    Gynecol Endocrinol; 2007 Feb; 23(2):94-8. PubMed ID: 17454159
    [Abstract] [Full Text] [Related]

  • 3. Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants.
    Çetin T, Turan İ.
    J Clin Res Pediatr Endocrinol; 2021 Aug 23; 13(3):362-366. PubMed ID: 33389921
    [Abstract] [Full Text] [Related]

  • 4. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK, Yung CH.
    Med J Malaysia; 2009 Sep 23; 64(3):242-3. PubMed ID: 20527279
    [Abstract] [Full Text] [Related]

  • 5. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, Lin-Su K, New MI.
    Endocrinol Metab Clin North Am; 2009 Dec 23; 38(4):699-718. PubMed ID: 19944288
    [Abstract] [Full Text] [Related]

  • 6. [Congenital adrenal hyperplasia due to 21 hydroxylase deficiency--case report].
    Vlaski J, Katanić D, Kavecan I, Dautović S, Vorgucin I.
    Med Pregl; 2008 Dec 23; 61(3-4):183-6. PubMed ID: 18773697
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Pubertal delay, hypokalemia, and hypertension caused by a rare form of congenital adrenal hyperplasia.
    Olson CA, Crudo DF.
    J Pediatr Adolesc Gynecol; 2011 Apr 10; 24(2):e29-31. PubMed ID: 21190871
    [Abstract] [Full Text] [Related]

  • 9. 17-Alpha hydroxylase deficiency: an unusual cause of secondary amenorrhoea.
    Philip J, Anjali, Thomas N, Rajaratnam S, Seshadri MS.
    Aust N Z J Obstet Gynaecol; 2004 Oct 10; 44(5):477-8. PubMed ID: 15387879
    [No Abstract] [Full Text] [Related]

  • 10. Primary amenorrhoea with hypertension: undiagnosed 17-α-hydroxylase deficiency.
    Britten FL, Ulett KB, Duncan EL, Perry-Keene DA.
    Med J Aust; 2013 Oct 21; 199(8):556-8. PubMed ID: 24138383
    [No Abstract] [Full Text] [Related]

  • 11. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency].
    Tosatti Júnior R, Souza HS, Tosatti A.
    Arq Bras Cardiol; 2005 Dec 21; 85(6):421-4. PubMed ID: 16429203
    [Abstract] [Full Text] [Related]

  • 12. Congenital adrenal hyperplasia with 11 beta-hydroxylase deficiency.
    Chang SH, Lee HH, Wang PJ, Chen JH, Chu SY.
    J Formos Med Assoc; 2004 Nov 21; 103(11):860-4. PubMed ID: 15549155
    [Abstract] [Full Text] [Related]

  • 13. A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation.
    Guenego A, Morel Y, Ionesco O, Mallet D, Priou-Guesdon M.
    Ann Endocrinol (Paris); 2015 Feb 21; 76(1):71-4. PubMed ID: 25613935
    [Abstract] [Full Text] [Related]

  • 14. Seventeen alpha-hydroxylase deficiency.
    Wong SL, Shu SG, Tsai CR.
    J Formos Med Assoc; 2006 Feb 21; 105(2):177-81. PubMed ID: 16477341
    [Abstract] [Full Text] [Related]

  • 15. Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations.
    Concolino P, Mello E, Zuppi C, Capoluongo E.
    Clin Chem Lab Med; 2010 Aug 21; 48(8):1057-62. PubMed ID: 20482300
    [Abstract] [Full Text] [Related]

  • 16. Diagnosis and management of classical congenital adrenal hyperplasia.
    Marumudi E, Khadgawat R, Surana V, Shabir I, Joseph A, Ammini AC.
    Steroids; 2013 Aug 21; 78(8):741-6. PubMed ID: 23624029
    [Abstract] [Full Text] [Related]

  • 17. [Congenital adrenal hyperplasia].
    Bouvattier C, Chatelain P.
    Rev Prat; 2008 May 15; 58(9):990-4. PubMed ID: 18672665
    [Abstract] [Full Text] [Related]

  • 18. [Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency].
    Krysiak R, Okopień B, Herman ZS.
    Pol Merkur Lekarski; 2006 Feb 15; 20(116):236-41. PubMed ID: 16708649
    [Abstract] [Full Text] [Related]

  • 19. 17-Hydroxyprogesterone in children, adolescents and adults.
    Honour JW.
    Ann Clin Biochem; 2014 Jul 15; 51(Pt 4):424-40. PubMed ID: 24711560
    [Abstract] [Full Text] [Related]

  • 20. Salt-wasting 21-hydroxylase deficiency congenital adrenal hyperplasia and pyloric stenosis in two Hispanic brothers.
    Pitukcheewanont P, Nimkarn S, Austin J, Sack Z, Fisher LK.
    J Pediatr; 2006 Aug 15; 149(2):268-70. PubMed ID: 16887450
    [Abstract] [Full Text] [Related]

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