Lista de obras - Valentina Cirello - Dominio Público Uruguay

A high percentage of BRAFV600E alleles in papillary thyroid carcinoma predicts a poorer outcome.

artículo científico publicado en 2012

Are pre-miR-146a and PTTG1 associated with papillary thyroid cancer?

scientific article published on 22 October 2013

BRAF mutations in an Italian cohort of thyroid cancers.

artículo científico publicado en 2004

Clinical and molecular analyses of thyroid cancer in patients treated for benign diseases

artículo científico publicado en 2013

Correlation between B-RAFV600E mutation and clinico-pathologic parameters in papillary thyroid carcinoma: data from a multicentric Italian study and review of the literature.

artículo científico publicado en 2006

Diabetes mellitus in a girl with thyroid hormone resistance syndrome: a little recognized interaction between the two diseases.

artículo científico publicado en 2014

Evidence of a low prevalence of RAS mutations in a large medullary thyroid cancer series.

artículo científico publicado en 2012

Fetal Cell Microchimerism in Papillary Thyroid Cancer: A Possible Role in Tumor Damage and Tissue Repair

artículo científico publicado en 2008

Fetal cell microchimerism in papillary thyroid cancer: A role in the outcome of the disease

artículo científico publicado en 2015

Fetal cell microchimerism in papillary thyroid cancer: studies in peripheral blood and tissues

artículo científico publicado en 2010

Fetal cell microchimerism: a protective role in autoimmune thyroid diseases

artículo científico publicado en 2015

Fetal microchimerism as an explanation of disease

artículo científico publicado en 2010

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

artículo científico publicado en 2007

Histopathological and molecular studies in patients with goiter and hypercalcitoninemia: reactive or neoplastic C-cell hyperplasia?

artículo científico publicado en 2007

Impact of estrogen and progesterone receptor expression on the clinical and molecular features of papillary thyroid cancer

artículo científico publicado en 2015

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.

artículo científico publicado en 2005

Microchimerism and Endocrine Disorders ⬇️

artículo científico publicado el 7 de marzo de 2012

Modifications in the Papillary Thyroid Cancer Gene Profile Over the Last 15 Years

article

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

artículo científico publicado en 2012

Novel insights into the link between fetal cell microchimerism and maternal cancers

artículo científico publicado en 2016

Oxidative stress and the subcellular localization of the telomerase reverse transcriptase (TERT) in papillary thyroid cancer.

artículo científico publicado en 2016

Positive effect of fetal cell microchimerism on tumor presentation and outcome in papillary thyroid cancer

artículo científico publicado en 2015

RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series

artículo científico publicado en 2008

Role of glucocorticoid receptor polymorphism in adrenal incidentalomas

artículo científico publicado en 2010

TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature.

artículo científico publicado en 2006

Telomerase in differentiated thyroid cancer: promoter mutations, expression and localization.

artículo científico publicado en 2014

The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects.

artículo científico publicado en 2013

The therapeutic outcome to intravenous steroid therapy for active Graves' orbitopathy is influenced by the time of response but not polymorphisms of the glucocorticoid receptor.

artículo científico publicado en 2013

The tight relationship between papillary thyroid cancer, autoimmunity and inflammation: clinical and molecular studies

artículo científico publicado en 2010

Total Iodide Organification Defect: Clinical and Molecular Characterization of an Italian Family

article

Lista de obras de Valentina Cirello

A high percentage of BRAFV600E alleles in papillary thyroid carcinoma predicts a poorer outcome.

Are pre-miR-146a and PTTG1 associated with papillary thyroid cancer?

BRAF mutations in an Italian cohort of thyroid cancers.

Clinical and molecular analyses of thyroid cancer in patients treated for benign diseases

Correlation between B-RAFV600E mutation and clinico-pathologic parameters in papillary thyroid carcinoma: data from a multicentric Italian study and review of the literature.

Diabetes mellitus in a girl with thyroid hormone resistance syndrome: a little recognized interaction between the two diseases.

Evidence of a low prevalence of RAS mutations in a large medullary thyroid cancer series.

Fetal Cell Microchimerism in Papillary Thyroid Cancer: A Possible Role in Tumor Damage and Tissue Repair

Fetal cell microchimerism in papillary thyroid cancer: A role in the outcome of the disease

Fetal cell microchimerism in papillary thyroid cancer: studies in peripheral blood and tissues

Fetal cell microchimerism: a protective role in autoimmune thyroid diseases

Fetal microchimerism as an explanation of disease

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

Histopathological and molecular studies in patients with goiter and hypercalcitoninemia: reactive or neoplastic C-cell hyperplasia?

Impact of estrogen and progesterone receptor expression on the clinical and molecular features of papillary thyroid cancer

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.

Microchimerism and Endocrine Disorders ⬇️

Modifications in the Papillary Thyroid Cancer Gene Profile Over the Last 15 Years

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

Novel insights into the link between fetal cell microchimerism and maternal cancers

Oxidative stress and the subcellular localization of the telomerase reverse transcriptase (TERT) in papillary thyroid cancer.

Positive effect of fetal cell microchimerism on tumor presentation and outcome in papillary thyroid cancer

RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series

Role of glucocorticoid receptor polymorphism in adrenal incidentalomas

TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature.

Telomerase in differentiated thyroid cancer: promoter mutations, expression and localization.

The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects.

The therapeutic outcome to intravenous steroid therapy for active Graves' orbitopathy is influenced by the time of response but not polymorphisms of the glucocorticoid receptor.

The tight relationship between papillary thyroid cancer, autoimmunity and inflammation: clinical and molecular studies

Total Iodide Organification Defect: Clinical and Molecular Characterization of an Italian Family