Thakker RV - Search Results

1

Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop.

Eastell R, Brandi ML, Costa AG, D'Amour P, Shoback DM, Thakker RV. Eastell R, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2014 Oct;99(10):3570-9. doi: 10.1210/jc.2014-1414. Epub 2014 Aug 27. J Clin Endocrinol Metab. 2014. PMID: 25162666

2

Neonatal primary hyperparathyroidism masked by vitamin D deficiency.

Meeran K, Husain M, Puccini M, Scott H, Dionisi-Vici C, Harvey DR, Lynn J, Thakker RV. Meeran K, et al. Among authors: thakker rv. Clin Endocrinol (Oxf). 1994 Oct;41(4):531-4. doi: 10.1111/j.1365-2265.1994.tb02586.x. Clin Endocrinol (Oxf). 1994. PMID: 7955463

3

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

Brandi ML, Gagel RF, Angeli A, Bilezikian JP, Beck-Peccoz P, Bordi C, Conte-Devolx B, Falchetti A, Gheri RG, Libroia A, Lips CJ, Lombardi G, Mannelli M, Pacini F, Ponder BA, Raue F, Skogseid B, Tamburrano G, Thakker RV, Thompson NW, Tomassetti P, Tonelli F, Wells SA Jr, Marx SJ. Brandi ML, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2001 Dec;86(12):5658-71. doi: 10.1210/jcem.86.12.8070. J Clin Endocrinol Metab. 2001. PMID: 11739416 Review.

4

A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis.

Lemos MC, Kotanko P, Christie PT, Harding B, Javor T, Smith C, Eastell R, Thakker RV. Lemos MC, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2005 Sep;90(9):5386-92. doi: 10.1210/jc.2004-2520. Epub 2005 Jun 28. J Clin Endocrinol Metab. 2005. PMID: 15985493

5

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, Besser GM, Conceição Pereira M, Davie MW, Dudley N, Leite V, Sadler GP, Seller A, Thakker RV. Bradley KJ, et al. Among authors: thakker rv. Clin Endocrinol (Oxf). 2006 Mar;64(3):299-306. doi: 10.1111/j.1365-2265.2006.02460.x. Clin Endocrinol (Oxf). 2006. PMID: 16487440

6

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene.

Hannan FM, Nesbit MA, Christie PT, Fratter C, Dudley NE, Sadler GP, Thakker RV. Hannan FM, et al. Among authors: thakker rv. Nat Clin Pract Endocrinol Metab. 2008 Jan;4(1):53-8. doi: 10.1038/ncpendmet0718. Nat Clin Pract Endocrinol Metab. 2008. PMID: 18084346

7

Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors.

Newey PJ, Jeyabalan J, Walls GV, Christie PT, Gleeson FV, Gould S, Johnson PR, Phillips RR, Ryan FJ, Shine B, Bowl MR, Thakker RV. Newey PJ, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2009 Oct;94(10):3640-6. doi: 10.1210/jc.2009-0564. Epub 2009 Jul 21. J Clin Endocrinol Metab. 2009. PMID: 19622622

8

A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome.

Gaynor KU, Grigorieva IV, Nesbit MA, Cranston T, Gomes T, Gortner L, Thakker RV. Gaynor KU, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2009 Oct;94(10):3897-904. doi: 10.1210/jc.2009-0717. Epub 2009 Sep 1. J Clin Endocrinol Metab. 2009. PMID: 19723756

9

Identification of a second kindred with familial hypocalciuric hypercalcemia type 3 (FHH3) narrows localization to a <3.5 megabase pair region on chromosome 19q13.3.

Nesbit MA, Hannan FM, Graham U, Whyte MP, Morrison PJ, Hunter SJ, Thakker RV. Nesbit MA, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2010 Apr;95(4):1947-54. doi: 10.1210/jc.2009-2152. Epub 2010 Feb 4. J Clin Endocrinol Metab. 2010. PMID: 20133464

10

A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism.

Mirczuk SM, Bowl MR, Nesbit MA, Cranston T, Fratter C, Allgrove J, Brain C, Thakker RV. Mirczuk SM, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2010 Jul;95(7):3512-6. doi: 10.1210/jc.2009-2532. Epub 2010 May 12. J Clin Endocrinol Metab. 2010. PMID: 20463099

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