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Mostrati risultati da 1 a 20 di 49
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
BRAF mutations in an Italian series of thyroid cancers 1-giu-2004 L. FugazzolaD. MannavolaV. CirelloG. VannucchiM. MuzzaP. Beck-Peccoz + Article (author) -
Absence of BRAF mutations in endocrine tumors 1-giu-2004 D. MannavolaV. CirelloM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
Total iodide organification defect : clinical and molecular characterization of an Italian family 1-gen-2005 L. FugazzolaD. MannavolaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
Gitelman’s sindrome : description of a new case in a family with RTH 1-mag-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 1-mag-2005 V. CirelloP. BraidottiM. MuzzaP. Beck PeccozS. BosariA. BastagliL. Fugazzola + Article (author) -
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 1-giu-2005 L. FugazzolaP. BraidottiV. CirelloP. Beck-PeccozS. BosariA. Bastagli + Article (author) -
Correlation between B-RAF(V600E) mutation and clinico-pathologic parameters in papillary thyroid carcinoma: data from a multicentric Italian study and review of the literature 1-gen-2006 L. FugazzolaV. CirelloD. MannavolaP. Beck-Peccoz + Article (author) -
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant 1-giu-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 1-giu-2006 G. VannucchiD. MannavolaV. CirelloI. CampiM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature 1-ott-2006 D. MannavolaG. VannucchiL. FugazzolaV. CirelloI. CampiL. PersaniP. Beck-Peccoz + Article (author) -
Histopathological and molecular studies in patients with goiter and hypercalcitoninemia : reactive or neoplastic C-cell hyperplasia? 1-gen-2007 S. Ferrero BogettoT. BrambillaV. CirelloM. MuzzaP. Beck PeccozL. Fugazzola + Article (author) -
The role of Ret genotypes as modifier loci for sporadic medullary cancer 1-gen-2007 M. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. PersaniL. Fugazzola + Article (author) -
Pendred’s sindrome : from genotype to phenotype 1-mar-2007 L. FugazzolaV. CirelloM. MuzzaP. Beck-Peccoz Article (author) -
RET genotypes comprising specific haplotypes of polymorphic variants are associated with sporadic medullary thyroid cancer 1-mag-2007 L. FugazzolaM. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
Fetal cell microchimerism in papillary thyroid cancer 1-set-2007 V. CirelloM. MuzzaM.P. RecalcatiM. PerrinoP. FinelliP. Beck-PeccozL. Fugazzola + Article (author) -
Fetal cell microchimerism in papillary thyroid cancer : a possible role in tumour demage and tissue repair 1-gen-2008 V. CirelloM. MuzzaP.L.M. Beck PeccozP. FinelliL. Fugazzola + Article (author) -
RET genotypes in sporadic medullary thyroid cancer : studies in a large Italian series 1-mar-2008 L. FugazzolaM. MuzzaD. CordellaV. CirelloP. Beck-PeccozL. Persani + Article (author) -
Fetal cell microchimerism in papillary thyroid cancer : a possibile role in tumor demage and tissue repair 1-mag-2008 V. CirelloM.P. RecalcatiM. MuzzaM. PerrinoP. Beck-PeccozP. FinelliL. Fugazzola + Article (author) -
Fetal microchimerism in women with thyroid cancer 1-giu-2008 V. CirelloM. MuzzaP. Beck-PeccozL. Fugazzola + Article (author) -
Fetal cell microchimerism in women with thyroid cancer 1-set-2008 V. CirelloM. PerrinoM. MuzzaP. Beck-PeccozL. Fugazzola + Book Part (author) -
Mostrati risultati da 1 a 20 di 49
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