Sfoglia per Autore
Genetic analyses and evaluation of peripheral parameters of thyroid hormone action for the differential diagnosis of RTH. A novel heterozygous missense mutation (M334T) discovered
2002 D. Mannavola, G. Vannucchi, L. Fugazzola, N. Cerutti, L. Persani, P. Beck-Peccoz
Multigenerational familial medullary thyroid cancer (FMTC): evidence for FMTC phenocopies and association with papillary thyroid cancer
2002 L. Fugazzola, N. Cerutti, D. Mannavola, G. Ghilardi, L. Alberti, R. Romoli, P. Beck-Peccoz
Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect
2003 L. Fugazzola, N. Cerutti, D. Mannavola, G. Vannucchi, C. Fallini, L. Persani, P. Beck-Peccoz
Frequent association between MEN 2A and cutaneous lichen amyloidosis
2003 U. Verga, L. Fugazzola, S. Cambiaghi, C. Pritelli, E. Alessi, D. Cortelazzi, E. Gangi, P. Beck-Peccoz
Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacement
2003 L. Fugazzola, L. Persani, D. Mannavola, E. Reschini, G. Vannucchi, G. Weber, P. Beck-Peccoz
BRAF mutations in an Italian series of thyroid cancers
2004 L. Fugazzola, D. Mannavola, V. Cirello, G. Vannucchi, M. Muzza, L. Vicentini, P. Beck-Peccoz
Absence of BRAF mutations in endocrine tumors
2004 D. Mannavola, V. Cirello, M. Muzza, P. Beck-Peccoz, L. Fugazzola
BRAF mutations in an Italian cohort of thyroid cancers
2004 L. Fugazzola, D. Mannavola, V. Cirello, G. Vannucchi, M. Muzza, L. Vicentini, P.L.M. Beck Peccoz
The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currents
2005 S. Dossena, A. Maccagni, V. Vezzoli, C. Bazzini, M.L. Garavaglia, G. Meyer, J. Fürst, M. Ritter, L. Fugazzola, L. Persani, P. Zorowka, C. Storelli, P. Beck-Peccoz, G. Bottà, M. Paulmichl
Different responses to chronic somatostatin analogues in patients with central hyperthyroidism
2005 D. Mannavola, L. Persani, G. Vannucchi, M. Zanardelli, L. Fugazzola, U. Verga, M. Facchetti, P. Beck-Peccoz
Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings
2005 M.C. Vigone, L. Fugazzola, I. Zamproni, A. Passoni, S. Di Candia, G. Chiumello, L. Persani, G. Weber
Total iodide organification defect : clinical and molecular characterization of an Italian family
2005 L. Fugazzola, D. Mannavola, M.C. Vigone, V. Cirello, G. Weber, P. Beck-Peccoz, L. Persani
Gitelman’s sindrome : description of a new case in a family with RTH
2005 D. Mannavola, G. Vannucchi, L. Fugazzola, M. Perrino, V. Cirello, M. Muzza, P. Beck Peccoz
Molecular analysis in three cases of medullary and papillary thyroid carcinoma occurring as collision tumors
2005 V. Cirello, S. Rossi, L. De Pasquale, P. Braidotti, M. Muzza, P. Beck Peccoz, S. Bosari, A. Bastagli, L. Fugazzola
Medullary and papillary carcinoma of the thyroid gland occurring as a collision tumour : report of three cases with molecular analysis and review of the literature
2005 S. Rossi, L. Fugazzola, L. De Pasquale, P. Braidotti, V. Cirello, P. Beck-Peccoz, S. Bosari, A. Bastagli
Radioiodine treatment of non-toxic multinodular goitre : effects of combination with lithium
2005 G. Vannucchi, A. Chiti, D. Mannavola, D. Dazzi, M. Rodari, S. Tadayyon, P. Beck-Peccoz, L. Fugazzola
Induction of a proinflammatory program in normal human thyrocytes by the RET/PTC1 oncogene
2005 M. Gariboldi, P. Allavena, P. Collini, M.G. Borrello, L. Alberti, A. Fischer, F. Marchesi, A. Greco, D. Degl'Innocenti, M.A. Pierotti, A. Mantovani, L. Fugazzola, P. Bressan, G. Cassinelli, S. Pilotti, C. Ferrario
Analisi funzionale di una complessa mutazione germinale localizzata nel dominio iuxtamembrana del gene RET in un carcinoma midollare familiare
2005 L. Fugazzola, D. Cordella, M. Muzza, L. Alberti, P. Travaglino, P. Colombo, P. Beck-Peccoz, L. Persani
Malattie del sistema endocrino diffuso, poliendocrinopatie, sindromi paraneoplastiche
2006 B. Ambrosi, L. Fugazzola, M. Peracchi, S. Corbetta
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
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