Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations

Best Practice and Research: Clinical Rheumatology

Volumn 22, Issue 1, 2008, Pages 129-148

  Egbuna, Ogo I ^a,b   Brown, Edward M ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

^b BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

Author keywords

acquired hypoparathyroidism; autosomal dominant hypoparathyroidism; Bartter's syndrome; calcilytic; calcimimetic; calcium homeostasis; calcium sensing receptor; familial hypocalciuric hypercalcaemia; hyperparathyroidism; mutations; osteoporosis; polymorphisms; seven transmembrane receptor

Indexed keywords

ALDOSTERONE ANTAGONIST; AMILORIDE; AMYLOID BETA PROTEIN; CALCILYTIC AGENT; CALCIMIMETIC AGENT; CALCIUM; CALCIUM ANTAGONIST; CALCIUM SENSING RECEPTOR; CINACALCET; GADOLINIUM; MAGNESIUM; N [3 (2 CHLOROPHENYL)PROPYL] 1 (3 METHOXYPHENYL)ETHYLAMINE; NEOMYCIN; PARATHYROID HORMONE; SPERMINE; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT DISORDER; BARTTER SYNDROME; CALCIUM CELL LEVEL; CALCIUM HOMEOSTASIS; CALCIUM METABOLISM; CALCIUM TRANSPORT; CELLULAR DISTRIBUTION; CHONDROGENESIS; DRUG MECHANISM; DRUG RECEPTOR BINDING; FAMILIAL DISEASE; FLUID THERAPY; GENE EXPRESSION REGULATION; GENE FUNCTION; GENE MUTATION; HETEROZYGOSITY; HORMONE RELEASE; HUMAN; HYPERCALCEMIA; HYPOCALCEMIA; HYPOKALEMIA; MOLECULAR MECHANICS; NEWBORN DISEASE; NONHUMAN; OSTEOLYSIS; OSTEOPOROSIS; PARATHYROID GLAND; PARATHYROIDECTOMY; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; REVIEW; SECONDARY HYPERPARATHYROIDISM; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 40149084169     PISSN: 15216942     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.berh.2007.11.006     Document Type: Review

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