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Journal Abstract Search

353 related items for PubMed ID: 12173690

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  • 2. Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.
    Hendy GN, D'Souza-Li L, Yang B, Canaff L, Cole DE.
    Hum Mutat; 2000 Oct; 16(4):281-96. PubMed ID: 11013439
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  • 3. The role of the extracellular calcium-sensing receptor in health and disease.
    Raue F, Haag C, Schulze E, Frank-Raue K.
    Exp Clin Endocrinol Diabetes; 2006 Sep; 114(8):397-405. PubMed ID: 17039419
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  • 4. Activating mutations of the Ca2+-sensing receptor.
    Mancilla EE, De Luca F, Baron J.
    Mol Genet Metab; 1998 Jul; 64(3):198-204. PubMed ID: 9719629
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  • 6. A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
    Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE.
    Nat Genet; 1995 Dec; 11(4):389-94. PubMed ID: 7493018
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  • 8. The pathophysiology of primary hyperparathyroidism.
    Brown EM.
    J Bone Miner Res; 2002 Nov; 17 Suppl 2():N24-9. PubMed ID: 12412774
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  • 10. 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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  • 12. Extracellular calcium-sensing receptor: structural and functional features and association with diseases.
    Hauache OM.
    Braz J Med Biol Res; 2001 May 10; 34(5):577-84. PubMed ID: 11323743
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  • 14. Calcium-sensing receptor (CaSR) mutations and disorders of calcium, electrolyte and water metabolism.
    Hannan FM, Thakker RV.
    Best Pract Res Clin Endocrinol Metab; 2013 Jun 10; 27(3):359-71. PubMed ID: 23856265
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  • 18. Inherited disorders of calcium homeostasis.
    Ramasamy I.
    Clin Chim Acta; 2008 Aug 10; 394(1-2):22-41. PubMed ID: 18474231
    [Abstract] [Full Text] [Related]

  • 19. Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.
    Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG.
    Nat Genet; 1994 Nov 10; 8(3):303-7. PubMed ID: 7874174
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  • 20. Disorders of the calcium-sensing receptor.
    Thakker RV.
    Biochim Biophys Acta; 1998 Dec 10; 1448(2):166-70. PubMed ID: 9920407
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