Amedei A - Search Results

1

Two novel mutations at exon 8 of the Sequestosome 1 (SQSTM1) gene in an Italian series of patients affected by Paget's disease of bone (PDB).

Falchetti A, Di Stefano M, Marini F, Del Monte F, Mavilia C, Strigoli D, De Feo ML, Isaia G, Masi L, Amedei A, Cioppi F, Ghinoi V, Bongi SM, Di Fede G, Sferrazza C, Rini GB, Melchiorre D, Matucci-Cerinic M, Brandi ML. Falchetti A, et al. Among authors: amedei a. J Bone Miner Res. 2004 Jun;19(6):1013-7. doi: 10.1359/JBMR.040203. Epub 2004 Feb 2. J Bone Miner Res. 2004. PMID: 15125799 Free article.

2

Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family.

Falchetti A, Di Stefano M, Marini F, Del Monte F, Gozzini A, Masi L, Tanini A, Amedei A, Carossino A, Isaia G, Brandi ML. Falchetti A, et al. Among authors: amedei a. Arthritis Res Ther. 2005;7(6):R1289-95. doi: 10.1186/ar1828. Epub 2005 Sep 15. Arthritis Res Ther. 2005. PMID: 16277682 Free PMC article.

3

Genetic aspects of the Paget's disease of bone: concerns on the introduction of DNA-based tests in the clinical practice. Advantages and disadvantages of its application.

Falchetti A, Marini F, Masi L, Amedei A, Brandi ML. Falchetti A, et al. Among authors: amedei a. Eur J Clin Invest. 2010 Jul;40(7):655-67. doi: 10.1111/j.1365-2362.2010.02312.x. Eur J Clin Invest. 2010. PMID: 20658751 Review.

4

The role of osteoprotegerin (OPG) and estrogen receptor (ER-α) gene polymorphisms in rheumatoid arthritis.

Masi L, Maddali Bongi S, Angotti C, Del Monte F, Carbonell Sala S, Basetti M, Amedei A, Falchetti A, Brandi ML. Masi L, et al. Among authors: amedei a. Clin Cases Miner Bone Metab. 2007 May;4(2):156-60. Clin Cases Miner Bone Metab. 2007. PMID: 22461216 Free PMC article.

5

Construction of a database for the evaluation and the clinical management of patients with breast cancer treated with antiestrogens and/or aromatase inhibitors.

Giusti F, Ottanelli S, Masi L, Amedei A, Brandi ML, Falchetti A. Giusti F, et al. Among authors: amedei a. Clin Cases Miner Bone Metab. 2011 Jan;8(1):37-50. Clin Cases Miner Bone Metab. 2011. PMID: 22461802 Free PMC article.

6

A novel recessive mutation of fibroblast growth factor-23 in tumoral calcinosis.

Masi L, Gozzini A, Franchi A, Campanacci D, Amedei A, Falchetti A, Franceschelli F, Marcucci G, Tanini A, Capanna R, Brandi ML. Masi L, et al. Among authors: amedei a. J Bone Joint Surg Am. 2009 May;91(5):1190-8. doi: 10.2106/JBJS.H.00783. J Bone Joint Surg Am. 2009. PMID: 19411468

7

A novel polymorphism at the GNAS1 gene associated with low circulating calcium levels.

Masi L, Del Monte F, Gozzini A, De Feo ML, Gionata Gheri R, Neri A, Falchetti A, Amedei A, Imbriaco R, Mavilia C, Tanini A, Brandi ML. Masi L, et al. Among authors: amedei a. Clin Cases Miner Bone Metab. 2007 May;4(2):139-45. Clin Cases Miner Bone Metab. 2007. PMID: 22461214 Free PMC article.

8

Polymorphism of the aromatase gene in postmenopausal Italian women: distribution and correlation with bone mass and fracture risk.

Masi L, Becherini L, Gennari L, Amedei A, Colli E, Falchetti A, Farci M, Silvestri S, Gonnelli S, Brandi ML. Masi L, et al. Among authors: amedei a. J Clin Endocrinol Metab. 2001 May;86(5):2263-9. doi: 10.1210/jcem.86.5.7450. J Clin Endocrinol Metab. 2001. PMID: 11344237

9

A patient with MEN1-associated hyperparathyroidism, responsive to cinacalcet.

Falchetti A, Cilotti A, Vaggelli L, Masi L, Amedei A, Cioppi F, Tonelli F, Brandi ML. Falchetti A, et al. Among authors: amedei a. Nat Clin Pract Endocrinol Metab. 2008 Jun;4(6):351-7. doi: 10.1038/ncpendmet0816. Epub 2008 Apr 15. Nat Clin Pract Endocrinol Metab. 2008. PMID: 18414463

10

Fracture unit: a (possible) model of implementation in Italy.

Falchetti A, Amedei A, Masi L, Giusti F, Cavalli L, Casentini C, Brandi ML. Falchetti A, et al. Among authors: amedei a. Clin Cases Miner Bone Metab. 2011 Jan;8(1):9-12. Clin Cases Miner Bone Metab. 2011. PMID: 22461796 Free PMC article.

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