Collins MT - Search Results

1

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. Among authors: collins mt. 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.

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. Among authors: collins mt. J Clin Endocrinol Metab. 2002 Nov;87(11):5104-12. doi: 10.1210/jc.2001-012022. J Clin Endocrinol Metab. 2002. PMID: 12414879

3

Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations.

Collins MT, Sarlis NJ, Merino MJ, Monroe J, Crawford SE, Krakoff JA, Guthrie LC, Bonat S, Robey PG, Shenker A. Collins MT, et al. J Clin Endocrinol Metab. 2003 Sep;88(9):4413-7. doi: 10.1210/jc.2002-021642. J Clin Endocrinol Metab. 2003. PMID: 12970318

4

Analyses of variable panoramic radiographic characteristics of maxillo-mandibular fibrous dysplasia in McCune-Albright syndrome.

Akintoye SO, Otis LL, Atkinson JC, Brahim J, Kushner H, Robey PG, Collins MT. Akintoye SO, et al. Among authors: collins mt. Oral Dis. 2004 Jan;10(1):36-43. doi: 10.1046/j.1354-523x.2003.00971.x. Oral Dis. 2004. PMID: 14996293

5

Fracture incidence in polyostotic fibrous dysplasia and the McCune-Albright syndrome.

Leet AI, Chebli C, Kushner H, Chen CC, Kelly MH, Brillante BA, Robey PG, Bianco P, Wientroub S, Collins MT. Leet AI, et al. Among authors: collins mt. J Bone Miner Res. 2004 Apr;19(4):571-7. doi: 10.1359/JBMR.0301262. Epub 2003 Dec 22. J Bone Miner Res. 2004. PMID: 15005844 Free article.

6

A novel technique based on a PNA hybridization probe and FRET principle for quantification of mutant genotype in fibrous dysplasia/McCune-Albright syndrome.

Karadag A, Riminucci M, Bianco P, Cherman N, Kuznetsov SA, Nguyen N, Collins MT, Robey PG, Fisher LW. Karadag A, et al. Among authors: collins mt. Nucleic Acids Res. 2004 Apr 19;32(7):e63. doi: 10.1093/nar/gnh059. Nucleic Acids Res. 2004. PMID: 15096559 Free PMC article.

7

Pegvisomant for the treatment of gsp-mediated growth hormone excess in patients with McCune-Albright syndrome.

Akintoye SO, Kelly MH, Brillante B, Cherman N, Turner S, Butman JA, Robey PG, Collins MT. Akintoye SO, et al. Among authors: collins mt. J Clin Endocrinol Metab. 2006 Aug;91(8):2960-6. doi: 10.1210/jc.2005-2661. Epub 2006 May 23. J Clin Endocrinol Metab. 2006. PMID: 16720661 Clinical Trial.

8

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

9

Letrozole treatment of precocious puberty in girls with the McCune-Albright syndrome: a pilot study.

Feuillan P, Calis K, Hill S, Shawker T, Robey PG, Collins MT. Feuillan P, et al. Among authors: collins mt. J Clin Endocrinol Metab. 2007 Jun;92(6):2100-6. doi: 10.1210/jc.2006-2350. Epub 2007 Apr 3. J Clin Endocrinol Metab. 2007. PMID: 17405850 Clinical Trial.

10

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.

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