Records 1 - 4 (of 4 Records)
|Query Trace: Hyperplasia and CASR[original query]|
| Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism.
European journal of endocrinology / European Federation of Endocrine Societies 2013 Nov 169 (5): 629-38.
Han Guiyan, Wang Ou, Nie Min, Zhu Yan, Meng Xunwu, Hu Yingying, Liu Huaicheng, Xing Xiaopi
| Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.
PloS one 2017 10 12 (10): e0186485.
Pardi Elena, Borsari Simona, Saponaro Federica, Bogazzi Fausto, Urbani Claudio, Mariotti Stefano, Pigliaru Francesca, Satta Chiara, Pani Fabiana, Materazzi Gabriele, Miccoli Paolo, Grantaliano Lorena, Marcocci Claudio, Cetani Filome
| Novel mutations of the calcium-sensing receptor impede differential diagnosis of primary hyperparathyroidism and familial hypocalciuric hypercalcemia.
Gland surgery 2022 3 11 (1): 12-22.
Bhangu Jagdeep Singh, Baumgartner-Parzer Sabina, Hargitai Lindsay, Mazal Peter, Scheuba Christian, Riss Phili
| Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 .
An Song, Yi Yang, Yue Jiang, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wa
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- Page last updated:Dec 04, 2023
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