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Items: 9

1.

Hyperparathyroid genes: sequences reveal answers and questions.

Marx SJ.

Endocr Pract. 2011 Jul-Aug;17 Suppl 3:18-27. doi: 10.4158/EP11067.RA. Review.

2.

Clinical and molecular genetics of parathyroid neoplasms.

Sharretts JM, Simonds WF.

Best Pract Res Clin Endocrinol Metab. 2010 Jun;24(3):491-502. doi: 10.1016/j.beem.2010.01.003. Review.

3.

Parathyroid carcinoma.

Givi B, Shah JP.

Clin Oncol (R Coll Radiol). 2010 Aug;22(6):498-507. doi: 10.1016/j.clon.2010.04.007. Epub 2010 May 26. Review.

4.

Parathyroid carcinoma.

Marcocci C, Cetani F, Rubin MR, Silverberg SJ, Pinchera A, Bilezikian JP.

J Bone Miner Res. 2008 Dec;23(12):1869-80. doi: 10.1359/jbmr.081018. Review. No abstract available.

5.

Genetic causes of hypercalciuric nephrolithiasis.

Stechman MJ, Loh NY, Thakker RV.

Pediatr Nephrol. 2009 Dec;24(12):2321-32. doi: 10.1007/s00467-008-0807-0. Epub 2008 Apr 30. Review.

6.

Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations.

Egbuna OI, Brown EM.

Best Pract Res Clin Rheumatol. 2008 Mar;22(1):129-48. doi: 10.1016/j.berh.2007.11.006. Review.

7.

Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.

Howell VM, Cardinal JW, Richardson AL, Gimm O, Robinson BG, Marsh DJ.

J Mol Diagn. 2006 Nov;8(5):559-66.

8.

Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14.

Warner JV, Nyholt DR, Busfield F, Epstein M, Burgess J, Stranks S, Hill P, Perry-Keene D, Learoyd D, Robinson B, Teh BT, Prins JB, Cardinal JW.

J Med Genet. 2006 Mar;43(3):e12.

9.

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing.

Cardinal JW, Bergman L, Hayward N, Sweet A, Warner J, Marks L, Learoyd D, Dwight T, Robinson B, Epstein M, Smith M, Teh BT, Cameron DP, Prins JB.

J Med Genet. 2005 Jan;42(1):69-74.

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