Persani L - Search Results

1

Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet.

Calebiro D, Porazzi P, Bonomi M, Lisi S, Grindati A, De Nittis D, Fugazzola L, Marinò M, Bottà G, Persani L. Calebiro D, et al. Among authors: persani l. J Endocrinol Invest. 2011 Sep;34(8):593-8. doi: 10.3275/7262. Epub 2010 Sep 9. J Endocrinol Invest. 2011. PMID: 20834201

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

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

Mutations of LH and FSH receptors.

Beck-Peccoz P, Romoli R, Persani L. Beck-Peccoz P, et al. Among authors: persani l. J Endocrinol Invest. 2000 Oct;23(9):566-72. doi: 10.1007/BF03343777. J Endocrinol Invest. 2000. PMID: 11079450 Review.

5

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

6

Loss of heterozygosity of the MEN1 gene in a large series of TSH-secreting pituitary adenomas.

Asteria C, Anagni M, Persani L, Beck-Peccoz P. Asteria C, et al. Among authors: persani l. J Endocrinol Invest. 2001 Nov;24(10):796-801. doi: 10.1007/BF03343929. J Endocrinol Invest. 2001. PMID: 11765049

7

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

8

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

9

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

10

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

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