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PUBMED FOR HANDHELDS

Journal Abstract Search


325 related items for PubMed ID: 10536001

  • 1. Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.
    New MI, Wilson RC.
    Proc Natl Acad Sci U S A; 1999 Oct 26; 96(22):12790-7. PubMed ID: 10536001
    [Abstract] [Full Text] [Related]

  • 2. Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment.
    Carlson AD, Obeid JS, Kanellopoulou N, Wilson RC, New MI.
    J Steroid Biochem Mol Biol; 1999 Oct 26; 69(1-6):19-29. PubMed ID: 10418977
    [Abstract] [Full Text] [Related]

  • 3. Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess.
    Cerame BI, New MI.
    J Pediatr Endocrinol Metab; 2000 Oct 26; 13(9):1537-47. PubMed ID: 11154148
    [Abstract] [Full Text] [Related]

  • 4. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Forest MG.
    Hum Reprod Update; 2004 Oct 26; 10(6):469-85. PubMed ID: 15514016
    [Abstract] [Full Text] [Related]

  • 5. An update of congenital adrenal hyperplasia.
    New MI.
    Ann N Y Acad Sci; 2004 Dec 26; 1038():14-43. PubMed ID: 15838095
    [Abstract] [Full Text] [Related]

  • 6. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Dec 26; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 7. Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
    Parsa AA, New MI.
    J Steroid Biochem Mol Biol; 2017 Jan 26; 165(Pt A):2-11. PubMed ID: 27380651
    [Abstract] [Full Text] [Related]

  • 8.
    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 Jan 26. PubMed ID: 20301350
    [Abstract] [Full Text] [Related]

  • 9. Genetics of adrenal steroid 21-hydroxylase deficiency.
    New MI, Speiser PW.
    Endocr Rev; 1986 Aug 26; 7(3):331-49. PubMed ID: 3527688
    [Abstract] [Full Text] [Related]

  • 10. Inborn errors of adrenal steroidogenesis.
    New MI.
    Mol Cell Endocrinol; 2003 Dec 15; 211(1-2):75-83. PubMed ID: 14656479
    [Abstract] [Full Text] [Related]

  • 11. Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family.
    Janjanin N, Dumic M, Skrabic V, Kusec V, Grubic Z, Spehar Uroic A.
    Horm Res; 2007 Dec 15; 67(3):111-6. PubMed ID: 17057407
    [Abstract] [Full Text] [Related]

  • 12. Steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia).
    New MI.
    Am J Med; 1995 Jan 16; 98(1A):2S-8S. PubMed ID: 7825636
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia.
    Cerame BI, Newfield RS, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC.
    J Clin Endocrinol Metab; 1999 Sep 16; 84(9):3129-34. PubMed ID: 10487675
    [Abstract] [Full Text] [Related]

  • 14. Antenatal diagnosis and treatment of congenital adrenal hyperplasia.
    New MI.
    Curr Urol Rep; 2001 Feb 16; 2(1):11-8. PubMed ID: 12084289
    [Abstract] [Full Text] [Related]

  • 15. Association between genotype, clinical presentation, and severity of congenital adrenal hyperplasia: a review.
    Al-Agha AE, Ocheltree AH, Al-Tamimi MD.
    Turk J Pediatr; 2012 Feb 16; 54(4):323-32. PubMed ID: 23692712
    [Abstract] [Full Text] [Related]

  • 16. Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood.
    White PC, Bachega TA.
    Semin Reprod Med; 2012 Oct 16; 30(5):400-9. PubMed ID: 23044877
    [Abstract] [Full Text] [Related]

  • 17. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    White PC, Speiser PW.
    Endocr Rev; 2000 Jun 16; 21(3):245-91. PubMed ID: 10857554
    [Abstract] [Full Text] [Related]

  • 18. Congenital adrenal hyperplasia: 11beta-hydroxylase deficiency.
    Peter M.
    Semin Reprod Med; 2002 Aug 16; 20(3):249-54. PubMed ID: 12428205
    [Abstract] [Full Text] [Related]

  • 19. Inherited forms of mineralocorticoid hypertension.
    White PC.
    Hypertension; 1996 Dec 16; 28(6):927-36. PubMed ID: 8952579
    [Abstract] [Full Text] [Related]

  • 20. Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.
    Ben Charfeddine I, Riepe FG, Kahloul N, Kulle AE, Adala L, Mamaï O, Amara A, Mili A, Amri F, Saad A, Holterhus PM, Gribaa M.
    Gen Comp Endocrinol; 2012 Feb 01; 175(3):514-8. PubMed ID: 22210247
    [Abstract] [Full Text] [Related]


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