Sfoglia per Autore
Activity and function of the nuclear factor kappaB pathway in human parathyroid tumors
2005-01-01 S. Corbetta, L. Vicentini, S. Ferrero, A. Lania, G. Mantovani, D. Cordella, P. Beck-Peccoz, A. Spada
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma
2006-01-01 D. Cordella, M. Muzza, L. Alberti, P. Colombo, P. Travaglini, P. Beck-Peccoz, L. Fugazzola, L. Persani
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma
2006-04-01 L. Fugazzola, D. Cordella, M. Muzza, L. Alberti, P. Travaglini, P. Colombo, P. Beck-Peccoz, L. Persani
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant
2006-06-01 L. Fugazzola, D. Cordella, V. Cirello, L. Alberti, M. Muzza, P. Beck Peccoz, L. Persani
The role of Ret genotypes as modifier loci for sporadic medullary cancer
2007-01-01 M. Muzza, D. Cordella, S. Barollo, L. Alberti, V. Cirello, D. Dazzi, M.E. Girelli, G. Opocher, P. Beck-Peccoz, L. Persani, L. Fugazzola
Prevalence on inactivating TSH receptor (TSHR) mutations in a large series of pediatric subjects with non-autoimmune mild hyper-thyrotropinemia (hyperTSH)
2007-01-01 D. Cordella, A. De Marco, D. Calebiro, T. De Filippis, G. Radaetti, G. Weber, M.C. Vigone, M. Cappa, A. Sartorio, M. Busnelli, M. Bonomi, B. Chini, P. Beck-Peccoz, L. Persani
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer
2007-05-01 L. Fugazzola, M. Muzza, C. Mian, D. Cordella, S. Barollo, V. Cirello, M.E. Girelli, G. Opocher, P. Beck-Peccoz, L. Persani
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series
2008-03-01 L. Fugazzola, M. Muzza, C. Mian, D. Cordella, S. Barollo, L. Alberti, V. Cirello, D. Dazzi, M.E. Girelli, G. Opocher, P. Beck-Peccoz, L. Persani
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION
2009-01-01 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, P. Beck-Peccoz, L. Persani, N. Italiano per lo studio dei Difetti Ovarici
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI)
2009-01-01 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, S. Bione, S. Cannavo, D. Bernard, T. Cole, J. Clayton Smith, P. Beck-Peccoz, L. Persani
Genetics and phenomics of hypothyroidism due to TSH resistance
2010-01-01 L. Persani, D. Calebiro, D. Cordella, G. Weber, G. Gelmini, D.V. Libri, T. De Filippis, M. Bonomi
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia
2012-01-01 D. Calebiro, G. Gelmini, D. Cordella, M. Bonomi, F. Winkler, H. Biebermann, A. De Marco, F. Marelli, D.V. Libri, F. Antonica, M.C. Vigone, M. Cappa, C. Mian, A. Sartorio, P. Beck Peccoz, G. Radetti, G. Weber, L. Persani
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