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Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.
Dumic KK, Grubic Z, Yuen T, Wilson RC, Kusec V, Barisic I, Stingl K, Sansovic I, Skrabic V, Dumic M, New MI. Dumic KK, et al. Among authors: wilson rc. J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):51-56. doi: 10.1016/j.jsbmb.2016.03.035. Epub 2016 Mar 31. J Steroid Biochem Mol Biol. 2017. PMID: 27041116
Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.
Yau M, Haider S, Khattab A, Ling C, Mathew M, Zaidi S, Bloch M, Patel M, Ewert S, Abdullah W, Toygar A, Mudryi V, Al Badi M, Alzubdi M, Wilson RC, Al Azkawi HS, Ozdemir HN, Abu-Amer W, Hertecant J, Razzaghy-Azar M, Funder JW, Al Senani A, Sun L, Kim SM, Yuen T, Zaidi M, New MI. Yau M, et al. Among authors: wilson rc. Proc Natl Acad Sci U S A. 2017 Dec 26;114(52):E11248-E11256. doi: 10.1073/pnas.1716621115. Epub 2017 Dec 11. Proc Natl Acad Sci U S A. 2017. PMID: 29229831 Free PMC article.
Hypertension and adrenal disorders.
Chemaitilly W, Wilson RC, New MI. Chemaitilly W, et al. Among authors: wilson rc. Curr Hypertens Rep. 2003 Dec;5(6):498-504. doi: 10.1007/s11906-003-0058-1. Curr Hypertens Rep. 2003. PMID: 14594571 Review.
373 results