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Mostrati risultati da 1 a 20 di 53
Titolo Data di pubblicazione Autori Tipo File Abstract
BRAF mutations in an Italian series of thyroid cancers 2004 L. FugazzolaD. MannavolaV. CirelloG. VannucchiM. MuzzaP. Beck-Peccoz + Article (author) -
Absence of BRAF mutations in endocrine tumors 2004 D. MannavolaV. CirelloM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
BRAF mutations in an Italian cohort of thyroid cancers 2004 L. FugazzolaM. MuzzaP.L.M. Beck Peccoz + Article (author) -
Gitelman’s sindrome : description of a new case in a family with RTH 2005 D. MannavolaG. VannucchiL. FugazzolaM. PerrinoV. CirelloM. MuzzaP. Beck Peccoz Article (author) -
Molecular analysis in three cases of medullary and papillary thyroid carcinoma occurring as collision tumors 2005 V. CirelloP. BraidottiM. MuzzaP. Beck PeccozS. BosariA. BastagliL. Fugazzola + Article (author) -
Analisi funzionale di una complessa mutazione germinale localizzata nel dominio iuxtamembrana del gene RET in un carcinoma midollare familiare 2005 L. FugazzolaM. MuzzaP. Beck-PeccozL. Persani + Conference Object -
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma 2006 D. CordellaM. MuzzaP. TravagliniP. Beck-PeccozL. FugazzolaL. Persani + Article (author) -
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma 2006 L. FugazzolaD. CordellaM. MuzzaP. Beck-PeccozL. Persani + Article (author) -
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant 2006 L. FugazzolaD. CordellaV. CirelloM. MuzzaP. Beck PeccozL. Persani + Article (author) -
Analysis of a deiodinase 2 polymorphism (oRFa-Asp) in patients with Graves’ disease and controls : preliminary results 2006 G. VannucchiD. MannavolaV. CirelloI. CampiM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
RET gene screening in patients with sporadic medullary thyroid carcinoma and functional characterization of a novel RET mutation 2006 M. MuzzaL. FugazzolaL. Persani + Article (author) -
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma 2006 M. MuzzaL. FugazzolaL. Persani + Article (author) -
Fetal cell microchimerism in papillary thyroid cancer 2007 M. MuzzaP. FinelliL. Fugazzola + Article (author) -
High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein 2007 L. FugazzolaS. DossenaS. RodighieroM. MuzzaU. AmbrosettiP. Beck-PeccozG. BottàM. Paulmichl + Article (author) -
The role of Ret genotypes as modifier loci for sporadic medullary cancer 2007 M. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. PersaniL. Fugazzola + Article (author) -
Histopathological and molecular studies in patients with goiter and hypercalcitoninemia : reactive or neoplastic C-cell hyperplasia? 2007 S. Ferrero BogettoT. BrambillaV. CirelloM. MuzzaP. Beck PeccozL. Fugazzola + Article (author) -
Pendred’s sindrome : from genotype to phenotype 2007 L. FugazzolaV. CirelloM. MuzzaP. Beck-Peccoz Article (author) -
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer 2007 L. FugazzolaM. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
Fetal cell microchimerism in papillary thyroid cancer 2007 V. CirelloM. MuzzaM.P. RecalcatiM. PerrinoP. FinelliP. Beck-PeccozL. Fugazzola + Article (author) -
Microchimerismo cellulare fetale nel carcinoma papillare della tiroide 2007 M. PerrinoM. MuzzaP. Beck-PeccozP. FinelliL. Fugazzola + Conference Object -
Mostrati risultati da 1 a 20 di 53
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