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Journal Abstract Search

216 related items for PubMed ID: 14696768

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  • 6. Familial hypocalciuric hypercalcemia caused by an R648stop mutation in the calcium-sensing receptor gene.
    Yamauchi M, Sugimoto T, Yamaguchi T, Yano S, Wang J, Bai M, Brown EM, Chihara K.
    J Bone Miner Res; 2002 Dec; 17(12):2174-82. PubMed ID: 12469911
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  • 9. Calcium regulation of parathyroid and C cell function in familial benign hypercalcemia.
    Rajala MM, Klee GG, Heath H.
    J Bone Miner Res; 1991 Feb; 6(2):117-24. PubMed ID: 2028833
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  • 11. [Severe neonatal hyperparathyroidism in a family with familial hypocalciuric hypercalcemia].
    Friis IM, Larsen NE, Lillquist K, Schwarz P.
    Ugeskr Laeger; 2000 Aug 14; 162(33):4402-3. PubMed ID: 10962966
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  • 12. [Familial hypocalciuric hypercalcemia: a new mutation].
    Ubetagoyena Arrieta M, Castaño González L, Pérez de Nanclares Leal G, Arruebarrena Lizarraga D, Imaz Murguiondo M, Areses Trapote R.
    An Pediatr (Barc); 2011 Jan 14; 74(1):47-50. PubMed ID: 21185797
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  • 14. Neonatal severe primary hyperparathyroidism and alkaptonuria in a boy born to related parents with familial hypocalciuric hypercalcemia.
    Steinmann B, Gnehm HE, Rao VH, Kind HP, Prader A.
    Helv Paediatr Acta; 1984 May 14; 39(2):171-86. PubMed ID: 6543841
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  • 19. An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds.
    Marx SJ, Attie MF, Spiegel AM, Levine MA, Lasker RD, Fox M.
    N Engl J Med; 1982 Feb 04; 306(5):257-64. PubMed ID: 7054696
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  • 20. Calcium infusion suggests a "set-point" abnormality of parathyroid gland function in familial benign hypercalcemia and more complex disturbances in primary hyperparathyroidism.
    Khosla S, Ebeling PR, Firek AF, Burritt MM, Kao PC, Heath H.
    J Clin Endocrinol Metab; 1993 Mar 04; 76(3):715-20. PubMed ID: 8445032
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