Condition: Hypercalcemia


rs104893689 in CASR gene and Hypercalcemia PMID 791660 1976 A comparison of the abilities of typical neuroleptic agents and of thioridazine, clozapine, sulpiride and metoclopramide to antagonise the hyperactivity induced by dopamine applied intracerebrally to areas of the extrapyramidal and mesolimbic systems.

PMID 8702647 1996 Expression and characterization of inactivating and activating mutations in the human Ca2+o-sensing receptor.

PMID 9011580 1997 In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.

PMID 15751724 2004 [Percutaneous tenotomy of achilles tendon in the treatment of congenital clubfeet--a preliminary report].

rs151344517 in LOC107985154;AFG3L2;TUBB6 gene and Hypercalcemia PMID 20725928 2010 Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.