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Journal Abstract Search

245 related items for PubMed ID: 12050233

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  • 11. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor.
    Pearce SH, Williamson C, Kifor O, Bai M, Coulthard MG, Davies M, Lewis-Barned N, McCredie D, Powell H, Kendall-Taylor P, Brown EM, Thakker RV.
    N Engl J Med; 1996 Oct 10; 335(15):1115-22. PubMed ID: 8813042
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  • 13. Autosomal dominant hypocalcemia: a novel activating mutation (E604K) in the cysteine-rich domain of the calcium-sensing receptor.
    Tan YM, Cardinal J, Franks AH, Mun HC, Lewis N, Harris LB, Prins JB, Conigrave AD.
    J Clin Endocrinol Metab; 2003 Feb 10; 88(2):605-10. PubMed ID: 12574188
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  • 16. Impaired growth and intracranial calcifications in autosomal dominant hypocalcemia caused by a GNA11 mutation.
    Tenhola S, Voutilainen R, Reyes M, Toiviainen-Salo S, Jüppner H, Mäkitie O.
    Eur J Endocrinol; 2016 Sep 10; 175(3):211-8. PubMed ID: 27334330
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  • 19. Activating mutations of the calcium-sensing receptor: management of hypocalcemia.
    Lienhardt A, Bai M, Lagarde JP, Rigaud M, Zhang Z, Jiang Y, Kottler ML, Brown EM, Garabédian M.
    J Clin Endocrinol Metab; 2001 Nov 10; 86(11):5313-23. PubMed ID: 11701698
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