Collins M - Search Results

1

Fracture Risk in Pediatric Patients With MEN2B.

Li I, Hartley IR, Klubo-Gwiedzdzinska J, Reynolds JC, Thomas BJ, Hogan J, Enyew MM, Dombi E, Ling A, Akshintala S, Venzon DJ, Del Rivero J, Collins M, Glod JW. Li I, et al. Among authors: collins m. J Clin Endocrinol Metab. 2022 Nov 25;107(12):e4371-e4378. doi: 10.1210/clinem/dgac500. J Clin Endocrinol Metab. 2022. PMID: 36056624 Free PMC article.

2

Characterization of gsp-mediated growth hormone excess in the context of McCune-Albright syndrome.

Akintoye SO, Chebli C, Booher S, Feuillan P, Kushner H, Leroith D, Cherman N, Bianco P, Wientroub S, Robey PG, Collins MT. Akintoye SO, et al. J Clin Endocrinol Metab. 2002 Nov;87(11):5104-12. doi: 10.1210/jc.2001-012022. J Clin Endocrinol Metab. 2002. PMID: 12414879

3

An instrument to measure skeletal burden and predict functional outcome in fibrous dysplasia of bone.

Collins MT, Kushner H, Reynolds JC, Chebli C, Kelly MH, Gupta A, Brillante B, Leet AI, Riminucci M, Robey PG, Bianco P, Wientroub S, Chen CC. Collins MT, et al. J Bone Miner Res. 2005 Feb;20(2):219-26. doi: 10.1359/JBMR.041111. Epub 2004 Nov 16. J Bone Miner Res. 2005. PMID: 15647815 Free article.

4

Determination of the elimination half-life of fibroblast growth factor-23.

Khosravi A, Cutler CM, Kelly MH, Chang R, Royal RE, Sherry RM, Wodajo FM, Fedarko NS, Collins MT. Khosravi A, et al. Among authors: collins mt. J Clin Endocrinol Metab. 2007 Jun;92(6):2374-7. doi: 10.1210/jc.2006-2865. Epub 2007 Mar 20. J Clin Endocrinol Metab. 2007. PMID: 17374707

5

The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndrome.

Celi FS, Coppotelli G, Chidakel A, Kelly M, Brillante BA, Shawker T, Cherman N, Feuillan PP, Collins MT. Celi FS, et al. Among authors: collins mt. J Clin Endocrinol Metab. 2008 Jun;93(6):2383-9. doi: 10.1210/jc.2007-2237. Epub 2008 Mar 18. J Clin Endocrinol Metab. 2008. PMID: 18349068 Free PMC article.

6

PTH(1-34) replacement therapy in a child with hypoparathyroidism caused by a sporadic calcium receptor mutation.

Theman TA, Collins MT, Dempster DW, Zhou H, Reynolds JC, Brahim JS, Roschger P, Klaushofer K, Winer KK. Theman TA, et al. J Bone Miner Res. 2009 May;24(5):964-73. doi: 10.1359/jbmr.081233. J Bone Miner Res. 2009. PMID: 19063686 Free PMC article.

7

Cushing syndrome in the McCune-Albright syndrome.

Brown RJ, Kelly MH, Collins MT. Brown RJ, et al. J Clin Endocrinol Metab. 2010 Apr;95(4):1508-15. doi: 10.1210/jc.2009-2321. Epub 2010 Feb 15. J Clin Endocrinol Metab. 2010. PMID: 20157193 Free PMC article.

8

Daily parathyroid hormone 1-34 replacement therapy for hypoparathyroidism induces marked changes in bone turnover and structure.

Gafni RI, Brahim JS, Andreopoulou P, Bhattacharyya N, Kelly MH, Brillante BA, Reynolds JC, Zhou H, Dempster DW, Collins MT. Gafni RI, et al. J Bone Miner Res. 2012 Aug;27(8):1811-20. doi: 10.1002/jbmr.1627. J Bone Miner Res. 2012. PMID: 22492501 Free PMC article. Clinical Trial.

9

Somatic GNAS mutation causes widespread and diffuse pituitary disease in acromegalic patients with McCune-Albright syndrome.

Vortmeyer AO, Gläsker S, Mehta GU, Abu-Asab MS, Smith JH, Zhuang Z, Collins MT, Oldfield EH. Vortmeyer AO, et al. J Clin Endocrinol Metab. 2012 Jul;97(7):2404-13. doi: 10.1210/jc.2012-1274. Epub 2012 May 7. J Clin Endocrinol Metab. 2012. PMID: 22564667 Free PMC article.

10

Characterization and management of testicular pathology in McCune-Albright syndrome.

Boyce AM, Chong WH, Shawker TH, Pinto PA, Linehan WM, Bhattacharryya N, Merino MJ, Singer FR, Collins MT. Boyce AM, et al. Among authors: collins mt. J Clin Endocrinol Metab. 2012 Sep;97(9):E1782-90. doi: 10.1210/jc.2012-1791. Epub 2012 Jun 28. J Clin Endocrinol Metab. 2012. PMID: 22745241 Free PMC article.

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