Beck-Peccoz P - Search Results

1

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. 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.

2

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. J Clin Endocrinol Metab. 2002 Jul;87(7):3201-8. doi: 10.1210/jcem.87.7.8653. J Clin Endocrinol Metab. 2002. PMID: 12107225

3

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. Clin Endocrinol (Oxf). 2003 Aug;59(2):230-6. doi: 10.1046/j.1365-2265.2003.01830.x. Clin Endocrinol (Oxf). 2003. PMID: 12864801

4

BRAF mutations in an Italian cohort of thyroid cancers.

Fugazzola L, Mannavola D, Cirello V, Vannucchi G, Muzza M, Vicentini L, Beck-Peccoz P. Fugazzola L, et al. Clin Endocrinol (Oxf). 2004 Aug;61(2):239-43. doi: 10.1111/j.1365-2265.2004.02089.x. Clin Endocrinol (Oxf). 2004. PMID: 15272920

5

Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies.

Fugazzola L, Cerutti N, Mannavola D, Crino A, Cassio A, Gasparoni P, Vannucchi G, Beck-Peccoz P. Fugazzola L, et al. Pediatr Res. 2002 Apr;51(4):479-84. doi: 10.1203/00006450-200204000-00013. Pediatr Res. 2002. PMID: 11919333

6

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. J Clin Endocrinol Metab. 1999 Feb;84(2):405-10. doi: 10.1210/jcem.84.2.5479. J Clin Endocrinol Metab. 1999. PMID: 10022392

7

The role of pendrin in iodide regulation.

Fugazzola L, Cerutti N, Mannavola D, Vannucchi G, Beck-Peccoz P. Fugazzola L, et al. Exp Clin Endocrinol Diabetes. 2001;109(1):18-22. doi: 10.1055/s-2001-11008. Exp Clin Endocrinol Diabetes. 2001. PMID: 11573133 Review.

8

Multigenerational familial medullary thyroid cancer (FMTC): evidence for FMTC phenocopies and association with papillary thyroid cancer.

Fugazzola L, Cerutti N, Mannavola D, Ghilardi G, Alberti L, Romoli R, Beck-Peccoz P. Fugazzola L, et al. Clin Endocrinol (Oxf). 2002 Jan;56(1):53-63. doi: 10.1046/j.0300-0664.2001.01434.x. Clin Endocrinol (Oxf). 2002. PMID: 11849247

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. J Clin Endocrinol Metab. 2003 Jul;88(7):3264-71. doi: 10.1210/jc.2002-021377. J Clin Endocrinol Metab. 2003. PMID: 12843174

10

The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects.

Muzza M, Rabbiosi S, Vigone MC, Zamproni I, Cirello V, Maffini MA, Maruca K, Schoenmakers N, Beccaria L, Gallo F, Park SM, Beck-Peccoz P, Persani L, Weber G, Fugazzola L. Muzza M, et al. J Clin Endocrinol Metab. 2014 Mar;99(3):E544-53. doi: 10.1210/jc.2013-3618. Epub 2013 Jan 1. J Clin Endocrinol Metab. 2014. PMID: 24423310

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