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Journal Abstract Search

358 related items for PubMed ID: 8575412

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  • 3. Human hypertension caused by mutations in the 11 beta-hydroxysteroid dehydrogenase gene: a molecular analysis of apparent mineralocorticoid excess.
    Whorwood CB, Stewart PM.
    J Hypertens Suppl; 1996 Dec; 14(5):S19-24. PubMed ID: 9120678
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  • 6. [Syndrome of apparent mineralocorticoid excess caused by a deficiency of 11 beta-hydroxysteroid dehydrogenase: clinical and genetic study in a Chilean family followed for 19 years].
    Rodríguez JA.
    Rev Med Chil; 2000 Jan; 128(1):17-26. PubMed ID: 10883518
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  • 9. Syndrome of apparent mineralocorticoid excess. A defect in the cortisol-cortisone shuttle.
    Stewart PM, Corrie JE, Shackleton CH, Edwards CR.
    J Clin Invest; 1988 Jul; 82(1):340-9. PubMed ID: 3164727
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  • 11. Apparent mineralocorticoid excess syndrome: report of one family with three affected children.
    Al-Harbi T, Al-Shaikh A.
    J Pediatr Endocrinol Metab; 2012 Jul; 25(11-12):1083-8. PubMed ID: 23329753
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  • 15. [11 beta-hydroxysteroid-dehydrogenase: characteristics and the clinical significance of a key enzyme in cortisol metabolism].
    Kerstens MN, Dullaart RP.
    Ned Tijdschr Geneeskd; 1999 Mar 06; 143(10):509-14. PubMed ID: 10321259
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  • 16. 11 beta-Hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess.
    White PC, Mune T, Rogerson FM, Kayes KM, Agarwal AK.
    Pediatr Res; 1997 Jan 06; 41(1):25-9. PubMed ID: 8979285
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  • 20. 11beta-hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess.
    White PC.
    Am J Med Sci; 2001 Dec 06; 322(6):308-15. PubMed ID: 11780688
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