Pinchera A - Search Results

1

Gain of function TSH receptor mutations and iodine deficiency: implications in iodine prophylaxis.

Tonacchera M, Vitti P, De Servi M, Agretti P, De Marco G, Chiovato L, Pinchera A. Tonacchera M, et al. Among authors: pinchera a. J Endocrinol Invest. 2003;26(2 Suppl):2-6. J Endocrinol Invest. 2003. PMID: 12762632 Review.

2

The sodium-iodide symporter protein is always present at a low expression and confined to the cell membrane in nonfunctioning nonadenomatous nodules of toxic nodular goitre.

Tonacchera M, Viacava P, Fanelli G, Agretti P, De Marco G, De Servi M, Di Cosmo C, Chiovato L, Pinchera A, Vitti P. Tonacchera M, et al. Among authors: pinchera a. Clin Endocrinol (Oxf). 2004 Jul;61(1):40-5. doi: 10.1111/j.1365-2265.2004.02047.x. Clin Endocrinol (Oxf). 2004. PMID: 15212643

3

Low prevalence of thyrotropin receptor mutations in a large series of subjects with sporadic and familial nonautoimmune subclinical hypothyroidism.

Tonacchera M, Perri A, De Marco G, Agretti P, Banco ME, Di Cosmo C, Grasso L, Vitti P, Chiovato L, Pinchera A. Tonacchera M, et al. Among authors: pinchera a. J Clin Endocrinol Metab. 2004 Nov;89(11):5787-93. doi: 10.1210/jc.2004-1243. J Clin Endocrinol Metab. 2004. PMID: 15531543

4

Identification of TSH receptor mutations in three families with resistance to TSH.

Tonacchera M, Di Cosmo C, De Marco G, Agretti P, Banco M, Perri A, Gianetti E, Montanelli L, Vitti P, Pinchera A. Tonacchera M, et al. Among authors: pinchera a. Clin Endocrinol (Oxf). 2007 Nov;67(5):712-8. doi: 10.1111/j.1365-2265.2007.02950.x. Epub 2007 Aug 13. Clin Endocrinol (Oxf). 2007. PMID: 17697008

5

Detection of antibodies blocking thyrotropin effect using Chinese hamster ovary cells transfected with the cloned human TSH receptor.

Chiovato L, Vitti P, Bendinelli G, Santini F, Fiore E, Capaccioli A, Tonacchera M, Mammoli C, Ludgate M, Pinchera A. Chiovato L, et al. Among authors: pinchera a. J Endocrinol Invest. 1994 Nov;17(10):809-16. doi: 10.1007/BF03347782. J Endocrinol Invest. 1994. PMID: 7699216

6

Transfection with the cDNA of the human thyrotropin receptor of a poorly differentiated rat thyroid cell line (FRT).

Elisei R, Pinchera A, Chiovato L, Mammoli C, Agretti P, Romei C, Santini F, Bendinelli G, Fiore E, Capaccioli A, Vitti P. Elisei R, et al. Among authors: pinchera a. J Endocrinol Invest. 1996 Apr;19(4):230-5. doi: 10.1007/BF03349873. J Endocrinol Invest. 1996. PMID: 8862503

7

Hyperfunctioning thyroid nodules in toxic multinodular goiter share activating thyrotropin receptor mutations with solitary toxic adenoma.

Tonacchera M, Chiovato L, Pinchera A, Agretti P, Fiore E, Cetani F, Rocchi R, Viacava P, Miccoli P, Vitti P. Tonacchera M, et al. Among authors: pinchera a. J Clin Endocrinol Metab. 1998 Feb;83(2):492-8. doi: 10.1210/jcem.83.2.4559. J Clin Endocrinol Metab. 1998. PMID: 9467563

8

[Physiopathology of iodine deficiency].

Pinchera A, Rago T, Vitti P. Pinchera A, et al. Ann Ist Super Sanita. 1998;34(3):301-5. Ann Ist Super Sanita. 1998. PMID: 10052165 Review. Italian.

9

Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene.

Tonacchera M, Agretti P, Pinchera A, Rosellini V, Perri A, Collecchi P, Vitti P, Chiovato L. Tonacchera M, et al. Among authors: pinchera a. J Clin Endocrinol Metab. 2000 Mar;85(3):1001-8. doi: 10.1210/jcem.85.3.6460. J Clin Endocrinol Metab. 2000. PMID: 10720030

10

Activating thyrotropin receptor mutations are present in nonadenomatous hyperfunctioning nodules of toxic or autonomous multinodular goiter.

Tonacchera M, Agretti P, Chiovato L, Rosellini V, Ceccarini G, Perri A, Viacava P, Naccarato AG, Miccoli P, Pinchera A, Vitti P. Tonacchera M, et al. Among authors: pinchera a. J Clin Endocrinol Metab. 2000 Jun;85(6):2270-4. doi: 10.1210/jcem.85.6.6634. J Clin Endocrinol Metab. 2000. PMID: 10852462

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