Familial hypocalciuric hypercalcemia associated with mutation in the human Ca(2+)-sensing receptor gene
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 98 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Genotype–Phenotype Correlations in Asian Indian Children and Adolescents with Primary Hyperparathyroidism;Calcified Tissue International;2022-05-14
2. The three common polymorphisms p.A986S, p.R990G and p.Q1011E in the calcium sensing receptor (CASR) are not associated with chronic pancreatitis;Pancreatology;2021-10
3. Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation;Hormone Research in Paediatrics;2020
4. Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene;The Journal of Clinical Endocrinology & Metabolism;2019-11-28
5. Parathyroid hormone-dependent familial hypercalcemia with low measured PTH levels and a presumptive novel pathogenic mutation in CaSR;Osteoporosis International;2019-10-23
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