Persani L - Search Results

1

Genetics and management of congenital hypothyroidism.

Persani L, Rurale G, de Filippis T, Galazzi E, Muzza M, Fugazzola L. Persani L, et al. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):387-396. doi: 10.1016/j.beem.2018.05.002. Epub 2018 May 19. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30086865 Review.

2

Circadian variations of thyrotropin bioactivity in normal subjects and patients with primary hypothyroidism.

Persani L, Terzolo M, Asteria C, Orlandi F, Angeli A, Beck-Peccoz P. Persani L, et al. J Clin Endocrinol Metab. 1995 Sep;80(9):2722-8. doi: 10.1210/jcem.80.9.7673415. J Clin Endocrinol Metab. 1995. PMID: 7673415

3

Evidence for the secretion of thyrotropin with enhanced bioactivity in syndromes of thyroid hormone resistance.

Persani L, Asteria C, Tonacchera M, Vitti P, Krishna V, Chatterjee K, Beck-Peccoz P. Persani L, et al. J Clin Endocrinol Metab. 1994 May;78(5):1034-9. doi: 10.1210/jcem.78.5.8175956. J Clin Endocrinol Metab. 1994. PMID: 8175956

4

Prenatal diagnosis of thyroid hormone resistance.

Asteria C, Rajanayagam O, Collingwood TN, Persani L, Romoli R, Mannavola D, Zamperini P, Buzi F, Ciralli F, Chatterjee VK, Beck-Peccoz P. Asteria C, et al. Among authors: persani l. J Clin Endocrinol Metab. 1999 Feb;84(2):405-10. doi: 10.1210/jcem.84.2.5479. J Clin Endocrinol Metab. 1999. PMID: 10022392

5

Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.

Fugazzola L, Mannavola D, Cerutti N, Maghnie M, Pagella F, Bianchi P, Weber G, Persani L, Beck-Peccoz P. Fugazzola L, et al. Among authors: persani l. J Clin Endocrinol Metab. 2000 Jul;85(7):2469-75. doi: 10.1210/jcem.85.7.6694. J Clin Endocrinol Metab. 2000. PMID: 10902795 Clinical Trial.

6

Circulating thyrotropin bioactivity in sporadic central hypothyroidism.

Persani L, Ferretti E, Borgato S, Faglia G, Beck-Peccoz P. Persani L, et al. J Clin Endocrinol Metab. 2000 Oct;85(10):3631-5. doi: 10.1210/jcem.85.10.6895. J Clin Endocrinol Metab. 2000. PMID: 11061514

7

Hyperplastic pituitary gland, high serum glycoprotein hormone alpha-subunit, and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH beta gene.

Bonomi M, Proverbio MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L. Bonomi M, et al. Among authors: persani l. J Clin Endocrinol Metab. 2001 Apr;86(4):1600-4. doi: 10.1210/jcem.86.4.7411. J Clin Endocrinol Metab. 2001. PMID: 11297590

8

Genetic analyses and evaluation of peripheral parameters of thyroid hormone action for the differential diagnosis of RTH. A novel heterozygous missense mutation (M334T) discovered.

Mannavola D, Vannucchi G, Fugazzola L, Cerutti N, Persani L, Beck-Peccoz P. Mannavola D, et al. Among authors: persani l. J Endocrinol Invest. 2002 Feb;25(2):RC4-6. doi: 10.1007/BF03343969. J Endocrinol Invest. 2002. PMID: 11929097

9

Central hypothyroidism: consequences in adult life.

Asteria C, Persani L, Beck-Peccoz P. Asteria C, et al. Among authors: persani l. J Pediatr Endocrinol Metab. 2001;14 Suppl 5:1263-9; discussion 1297-8. J Pediatr Endocrinol Metab. 2001. PMID: 11964021 Review.

10

Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.

Alberti L, Proverbio MC, Costagliola S, Romoli R, Boldrighini B, Vigone MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L. Alberti L, et al. Among authors: persani l. J Clin Endocrinol Metab. 2002 Jun;87(6):2549-55. doi: 10.1210/jcem.87.6.8536. J Clin Endocrinol Metab. 2002. PMID: 12050212

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

385 results

Search Page