Persani L - Search Results

1

New genetics in congenital hypothyroidism.

Stoupa A, Kariyawasam D, Muzza M, de Filippis T, Fugazzola L, Polak M, Persani L, Carré A. Stoupa A, et al. Among authors: persani l. Endocrine. 2021 Mar;71(3):696-705. doi: 10.1007/s12020-021-02646-9. Epub 2021 Mar 1. Endocrine. 2021. PMID: 33650047 Review.

2

Evaluation of the adequacy of levothyroxine replacement therapy in patients with central hypothyroidism.

Ferretti E, Persani L, Jaffrain-Rea ML, Giambona S, Tamburrano G, Beck-Peccoz P. Ferretti E, et al. Among authors: persani l. J Clin Endocrinol Metab. 1999 Mar;84(3):924-9. doi: 10.1210/jcem.84.3.5553. J Clin Endocrinol Metab. 1999. PMID: 10084572 Clinical Trial.

3

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.

4

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

5

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.

6

Highly sensitive serum thyroglobulin and circulating thyroglobulin mRNA evaluations in the management of patients with differentiated thyroid cancer in apparent remission.

Fugazzola L, Mihalich A, Persani L, Cerutti N, Reina M, Bonomi M, Ponti E, Mannavola D, Giammona E, Vannucchi G, di Blasio AM, Beck-Peccoz P. Fugazzola L, et al. Among authors: persani l. J Clin Endocrinol Metab. 2002 Jul;87(7):3201-8. doi: 10.1210/jcem.87.7.8653. J Clin Endocrinol Metab. 2002. PMID: 12107225

7

Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect.

Fugazzola L, Cerutti N, Mannavola D, Vannucchi G, Fallini C, Persani L, Beck-Peccoz P. Fugazzola L, et al. Among authors: persani l. J Clin Endocrinol Metab. 2003 Jul;88(7):3264-71. doi: 10.1210/jc.2002-021377. J Clin Endocrinol Metab. 2003. PMID: 12843174

8

Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacement.

Fugazzola L, Persani L, Mannavola D, Reschini E, Vannucchi G, Weber G, Beck-Peccoz P. Fugazzola L, et al. Among authors: persani l. Clin Endocrinol (Oxf). 2003 Aug;59(2):230-6. doi: 10.1046/j.1365-2265.2003.01830.x. Clin Endocrinol (Oxf). 2003. PMID: 12864801

9

Different responses to chronic somatostatin analogues in patients with central hyperthyroidism.

Mannavola D, Persani L, Vannucchi G, Zanardelli M, Fugazzola L, Verga U, Facchetti M, Beck-Peccoz P. Mannavola D, et al. Among authors: persani l. Clin Endocrinol (Oxf). 2005 Feb;62(2):176-81. doi: 10.1111/j.1365-2265.2004.02192.x. Clin Endocrinol (Oxf). 2005. PMID: 15670193

10

Congenital hypothyroidism with gland in situ: diagnostic re-evaluation.

Weber G, Vigone MC, Passoni A, Odoni M, Paesano PL, Dosio F, Proverbio MC, Corbetta C, Persani L, Chiumello G. Weber G, et al. Among authors: persani l. J Endocrinol Invest. 2005 Jun;28(6):516-22. doi: 10.1007/BF03347239. J Endocrinol Invest. 2005. PMID: 16117192

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