CORDELLA, DANIELA
CORDELLA, DANIELA
Universita' degli Studi di MILANO
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia
2012 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
Genetics and phenomics of hypothyroidism due to TSH resistance
2010 L. Persani, D. Calebiro, D. Cordella, G. Weber, G. Gelmini, D.V. Libri, T. De Filippis, M. Bonomi
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI)
2009 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, S. Bione, S. Cannavo, D. Bernard, T. Cole, J. Clayton Smith, P. Beck-Peccoz, L. Persani
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION
2009 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, P. Beck-Peccoz, L. Persani, N. Italiano per lo studio dei Difetti Ovarici
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series
2008 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
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer
2007 L. Fugazzola, M. Muzza, C. Mian, D. Cordella, S. Barollo, V. Cirello, M.E. Girelli, G. Opocher, P. Beck-Peccoz, L. Persani
The role of Ret genotypes as modifier loci for sporadic medullary cancer
2007 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 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
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant
2006 L. Fugazzola, D. Cordella, V. Cirello, L. Alberti, M. Muzza, P. Beck Peccoz, L. Persani
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma
2006 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 L. Fugazzola, D. Cordella, M. Muzza, L. Alberti, P. Travaglini, P. Colombo, P. Beck-Peccoz, L. Persani
Activity and function of the nuclear factor kappaB pathway in human parathyroid tumors
2005 S. Corbetta, L. Vicentini, S. Ferrero, A. Lania, G. Mantovani, D. Cordella, P. Beck-Peccoz, A. Spada