Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene

Author:

Hannan Fadil M,Nesbit M Andrew,Christie Paul T,Fratter Carl,Dudley Nicholas E,Sadler Greg P,Thakker Rajesh V

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference24 articles.

1. Thakker RV (2006) Multiple Endocrine Neoplasia Type 1. I. Endocrinology, 3509–3531 (Eds DeGroot LJ and Jameson JL) Philadelphia, PA: WB Saunders

2. Bradley KJ et al. (2005) Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. J Intern Med 257: 18–26

3. Hoff AO and Gagel RF (2006) Multiple Endocrine Neoplasia Type 2. I. Endocrinology, 3533–3550 (Eds DeGroot LJ and Jameson JL) Philadelphia, PA: WB Saunders

4. Adami S et al. (2002) Epidemiology of primary hyperparathyroidism in Europe. J Bone Miner Res 17 (Suppl 2): N18–N23

5. Pannett AA et al. (2003) Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. Clin Endocrinol (Oxf) 58: 639–646

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