Familial hypocalciuric hypercalcemia associated with crystal deposition disease
Author:
Publisher
Elsevier BV
Subject
Rheumatology
Reference12 articles.
1. Two Italian kindreds with familial hypocalciuric hypercalcemia caused by loss-of-function mutations in the calcium-sensing receptor (CaR) gene: functional characterization of a novel CaR missense mutation;Cetani;Clin Endocrinol (Oxf),2003
2. http://www.casrdb.mcgill.ca/.
3. Extracellular calcium sensing and extracellular calcium signaling;Brown;Physiol Rev,2001
4. Bone-mineral density in patients with familial hypocalciuric hypercalcaemia (FHH);Abugassa;Eur J Surg,1992
5. The prevalence of knee osteoarthritis in the elderly. The Framingham Osteoarthritis Study;Felson;Arthritis Rheum,1987
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1. Calcium Pyrophosphate Crystal Deposition: Insights to Risks Factors and Associated Conditions;Current Rheumatology Reports;2024-08-05
2. Case report: familial hypocalciuric hypercalcemia;AME Case Reports;2024-04
3. Expanding the phenotype of familial hypocalciuric hypercalcemia type 3: Case report and review of the literature;Journal of Clinical and Translational Endocrinology: Case Reports;2022-12
4. Heterozygous Mutation (Q459R) in the Calcium-Sensing Receptor Gene Causes Familial Hypocalciuric Hypercalcemia 1 (FHH1);The Journal of Clinical Endocrinology & Metabolism;2019-11-18
5. Conventional Radiology in Crystal Arthritis;Radiologic Clinics of North America;2017-09
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