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A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia.
Lietman SA, Tenenbaum-Rakover Y, Jap TS, Yi-Chi W, De-Ming Y, Ding C, Kussiny N, Levine MA. Lietman SA, et al. Among authors: levine ma. J Clin Endocrinol Metab. 2009 Nov;94(11):4372-9. doi: 10.1210/jc.2008-2484. Epub 2009 Sep 29. J Clin Endocrinol Metab. 2009. PMID: 19789209 Free PMC article.
Fibrous dysplasia.
Lietman SA, Levine MA. Lietman SA, et al. Among authors: levine ma. Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2:389-96. Pediatr Endocrinol Rev. 2013. PMID: 23858622 Review.
SH3BP2 is an activator of NFAT activity and osteoclastogenesis.
Lietman SA, Yin L, Levine MA. Lietman SA, et al. Among authors: levine ma. Biochem Biophys Res Commun. 2008 Jul 11;371(4):644-8. doi: 10.1016/j.bbrc.2008.04.080. Epub 2008 Apr 25. Biochem Biophys Res Commun. 2008. PMID: 18440306 Free PMC article.
Hypercalcemia in children and adolescents.
Lietman SA, Germain-Lee EL, Levine MA. Lietman SA, et al. Among authors: levine ma. Curr Opin Pediatr. 2010 Aug;22(4):508-15. doi: 10.1097/MOP.0b013e32833b7c23. Curr Opin Pediatr. 2010. PMID: 20601885 Free PMC article. Review.
532 results