Three Inherited Disorders of Calcium Sensing
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference41 articles.
1. Familial Isolated Hypoparathyroidism
2. Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene
3. Monoclonality and Abnormal Parathyroid Hormone Genes in Parathyroid Adenomas
4. Urinary calcium excretion in familial hypocalciuric hypercalcemia. Persistence of relative hypocalciuria after induction of hypoparathyroidism
5. A Comparison of the Effects of Divalent and Trivalent Cations on Parathyroid Hormone Release, 3′,5′-Cyclic-Adenosine Monophosphate Accumulation, and the Levels of Inositol Phosphates in Bovine Parathyroid Cells
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2. Single Gland, Ectopic Location: Adenomas are Common Causes of Primary Hyperparathyroidism in Children and Adolescents;World Journal of Surgery;2020-01-03
3. Parathyroid Hormone;Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism;2018-09-28
4. Rationale to reduce calcium intake in adult patients with chronic kidney disease;Current Opinion in Nephrology and Hypertension;2018-07
5. Calcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis;Clinical Journal of the American Society of Nephrology;2017-06-19
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