MUZZA, MARINA

MUZZA, MARINA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 55 (tempo di esecuzione: 0.009 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Absence of BRAF mutations in endocrine tumors 1-giu-2004 D. MannavolaV. CirelloM. MuzzaP. Beck-PeccozL. Fugazzola Article (author) -
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis 1-nov-2008 M. MuzzaL. PersaniP. Beck PeccozL. Fugazzola + Article (author) -
Absence of sonic hedgehog mutations in a large cohort of children with thyroid dysgenesis 1-mag-2008 M. MuzzaP. Beck-PeccozL. PersaniL. Fugazzola + 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) -
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma 1-gen-2006 D. CordellaM. MuzzaP. TravagliniP. Beck-PeccozL. FugazzolaL. Persani + Article (author) -
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma 1-set-2006 M. MuzzaL. FugazzolaL. Persani + Article (author) -
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma 1-apr-2006 L. FugazzolaD. CordellaM. MuzzaP. Beck-PeccozL. Persani + Article (author) -
Analisi funzionale di una complessa mutazione germinale localizzata nel dominio iuxtamembrana del gene RET in un carcinoma midollare familiare 1-dic-2005 L. FugazzolaM. MuzzaP. Beck-PeccozL. Persani + Conference Object -
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) -
BRAF mutations in an Italian cohort of thyroid cancers 1-ago-2004 L. FugazzolaM. MuzzaP.L.M. Beck Peccoz + Article (author) -
BRAF mutations in an Italian series of thyroid cancers 1-giu-2004 L. FugazzolaD. MannavolaV. CirelloG. VannucchiM. MuzzaP. Beck-Peccoz + Article (author) -
Combined Mutational and Clonality Analyses Support the Existence of Intra-Tumor Heterogeneity in Papillary Thyroid Cancer 1-gen-2021 Marina MuzzaGabriele PogliaghiLuca PersaniLaura FugazzolaCarla Colombo Article (author) -
Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism 1-set-2017 Muzza MFugazzola LPersani L + Article (author) -
Disorders of H2O2 generation 1-mar-2017 Muzza, MarinaFugazzola, Laura Article (author) -
DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom 1-giu-2019 Muzza MFugazzola L + Article (author) -
DUOXS defects : genotype-phenotype correlations 1-apr-2011 L. FugazzolaM. MuzzaP. Beck PeccozL. Persani + Article (author) -
FAM83B is involved in thyroid cancer cell differentiation and migration 1-gen-2022 Cirello VGrassi ESPogliaghi GGhiandai VMuzza MPersani LColombo CFugazzola L. + 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 1-gen-2007 M. MuzzaP. FinelliL. Fugazzola + 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) -