Hyperparathyroidism in Complex Genetic Disorders
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-89497-3_15
Reference26 articles.
1. Alevizaki M, Saltiki K. Primary hyperparathyroidism in MEN2 syndromes. Recent Results Cancer Res. 2015;204:179–86.
2. Alrezk R, Hannah-Shmouni F, Stratakis CA. MEN4 and CDKN1B mutations: the latest of the MEN syndromes. Endocr Relat Cancer. 2017;24(10):T195–208.
3. Balsalobre Salmeron M, Rodriguez Gonzalez JM, Ríos A, Febrero B, Parrilla Paricio P. Primary hyperparathyroidism associated with MEN 1: experience in 71 cases. Cir Esp. 2018;96(10):627–33.
4. DeLellis RA, Mangray S. Heritable forms of primary hyperparathyroidism: a current perspective. Histopathology. 2018;72(1):117–32.
5. El Lakis M, Nockel P, Guan B, Agarwal S, Welch J, Simonds WF, et al. Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure. Surgery. 2018a;163(1):31–4.
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