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European Journal of Endocrinology
|
September 4, 2007
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
Laura Fugazzola, Valentina Cirello, Silvia Dossena, et al.
Scientific Reports
|
March 15, 2019
The BRAF-inhibitor PLX4720 inhibits CXCL8 secretion in BRAFV600E mutated and normal thyroid cells: a further anti-cancer effect of BRAF-inhibitors
Francesca Coperchini, Laura Croce, Marco Denegri, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 3, 2019
<i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom
Catherine Peters, Adeline K Nicholas, Erik Schoenmakers, et al.
Clinical Endocrinology
|
April 16, 2008
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis
Marina Muzza, Luca Persani, Tiziana de Filippis, et al.
Clinical Endocrinology
|
February 21, 2008
RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series
Laura Fugazzola, Marina Muzza, Caterina Mian, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
November 17, 2020
The molecular and gene/miRNA expression profiles of radioiodine resistant papillary thyroid cancer
Carla Colombo, Emanuela Minna, Chiara Gargiuli, et al.
Endocrine-Related Cancer
|
November 19, 2025
Clinical relevance of the thyroid differentiation score (TDS) in benign and malignant thyroid tumors
Marina Muzza, Carla Colombo, Gabriele Pogliaghi, et al.
Molecular and Cellular Endocrinology
|
January 31, 2012
Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss
Valentina Cirello, Claudia Bazzini, Valeria Vezzoli, et al.
Molecular and Cellular Endocrinology
|
December 3, 2014
Telomerase in differentiated thyroid cancer: promoter mutations, expression and localization
Marina Muzza, Carla Colombo, Stefania Rossi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 30, 2012
Modifications in the papillary thyroid cancer gene profile over the last 15 years
Cristina Romei, Laura Fugazzola, Efisio Puxeddu, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
European Journal of Endocrinology
|
September 4, 2007
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
Laura Fugazzola, Valentina Cirello, Silvia Dossena, et al.
Scientific Reports
|
March 15, 2019
The BRAF-inhibitor PLX4720 inhibits CXCL8 secretion in BRAFV600E mutated and normal thyroid cells: a further anti-cancer effect of BRAF-inhibitors
Francesca Coperchini, Laura Croce, Marco Denegri, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 3, 2019
<i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom
Catherine Peters, Adeline K Nicholas, Erik Schoenmakers, et al.
Clinical Endocrinology
|
April 16, 2008
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis
Marina Muzza, Luca Persani, Tiziana de Filippis, et al.
Clinical Endocrinology
|
February 21, 2008
RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series
Laura Fugazzola, Marina Muzza, Caterina Mian, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
November 17, 2020
The molecular and gene/miRNA expression profiles of radioiodine resistant papillary thyroid cancer
Carla Colombo, Emanuela Minna, Chiara Gargiuli, et al.
Endocrine-Related Cancer
|
November 19, 2025
Clinical relevance of the thyroid differentiation score (TDS) in benign and malignant thyroid tumors
Marina Muzza, Carla Colombo, Gabriele Pogliaghi, et al.
Molecular and Cellular Endocrinology
|
January 31, 2012
Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss
Valentina Cirello, Claudia Bazzini, Valeria Vezzoli, et al.
Molecular and Cellular Endocrinology
|
December 3, 2014
Telomerase in differentiated thyroid cancer: promoter mutations, expression and localization
Marina Muzza, Carla Colombo, Stefania Rossi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 30, 2012
Modifications in the papillary thyroid cancer gene profile over the last 15 years
Cristina Romei, Laura Fugazzola, Efisio Puxeddu, et al.
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of 5