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Journal Abstract Search

105 related items for PubMed ID: 8487479

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  • 3. Congenital adrenal hyperplasia due to 11-hydroxylase enzyme deficiency in three siblings. A brief report.
    Agboola-Abu CF, Aligwekwe PK, Olowu AO, Kuku SF.
    West Afr J Med; 1999; 18(2):80-6. PubMed ID: 10504861
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  • 11. [Late reattribution of sex: a clinical example].
    Bregani P, Gargantini L, Lauri S, Nizzoli G, Trifirò G, Chiumello G.
    Pediatr Med Chir; 1983; 5(1-2):103-6. PubMed ID: 6634432
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  • 12. Congenital adrenal hyperplasia due to deficient cholesterol side-chain cleavage activity (20, 22-desmolase) in a patient treated for 18 years.
    Hauffa BP, Miller WL, Grumbach MM, Conte FA, Kaplan SL.
    Clin Endocrinol (Oxf); 1985 Nov; 23(5):481-93. PubMed ID: 3841304
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  • 13. [Primary adrenal insufficiency in children].
    Rijlaarsdam RS, van Diepen MM, Wit JM.
    Ned Tijdschr Geneeskd; 2005 May 21; 149(21):1137-41. PubMed ID: 15940915
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  • 14. Molecular and structural analysis of two novel StAR mutations in patients with lipoid congenital adrenal hyperplasia.
    Achermann JC, Meeks JJ, Jeffs B, Das U, Clayton PE, Brook CG, Jameson JL.
    Mol Genet Metab; 2001 Aug 21; 73(4):354-7. PubMed ID: 11509019
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  • 16. Molecular basis of adrenal insufficiency.
    Fujieda K, Tajima T.
    Pediatr Res; 2005 May 21; 57(5 Pt 2):62R-69R. PubMed ID: 15817507
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  • 18. [20,22 Desmolase deficiency].
    Fujieda K.
    Nihon Rinsho; 2006 May 28; Suppl 1():696-8. PubMed ID: 16776251
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