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Cancers
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December 11, 2022
Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer
Marina Muzza, Gabriele Pogliaghi, Carla Colombo, et al.
Frontiers in Endocrinology
|
July 28, 2022
Unilateral Surgery for Medullary Thyroid Carcinoma: Seeking for Clinical Practice Guidelines
Daqi Zhang, Carla Colombo, Hui Sun, et al.
European Thyroid Journal
|
July 4, 2024
2024 European Thyroid Association Guidelines on diagnosis and management of genetic disorders of thyroid hormone transport, metabolism and action
Luca Persani, Patrice Rodien, Carla Moran, et al.
European Thyroid Journal
|
April 24, 2024
Radiofrequency ablation is an effective treatment for Bethesda III thyroid nodules without genetic alterations
Laura Fugazzola, Maurilio Deandrea, Stefano Borgato, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
October 13, 2018
Effects of human recombinant type I IFNs (IFN-α2b and IFN-β1a) on growth and migration of primary endometrial stromal cells from women with deeply infiltrating endometriosis: A preliminary study
Alessandra Dicitore, Sara Castiglioni, Davide Saronni, et al.
Frontiers in Endocrinology
|
December 19, 2022
Genetic and phenotypic differences between sexes in congenital hypogonadotropic hypogonadism (CHH): Large cohort analysis from a single tertiary centre
Silvia Federici, Biagio Cangiano, Giovanni Goggi, 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.
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.
The Journal of Clinical Endocrinology and Metabolism
|
June 7, 2002
Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism
Luisella Alberti, Maria Carla Proverbio, Sabine Costagliola, et al.
BMC Medical Genetics
|
May 7, 2011
SNPs and real-time quantitative PCR method for constitutional allelic copy number determination, the VPREB1 marker case
Marcello Frigerio, Elena Passeri, Tiziana de Filippis, et al.
Page
of 33
Search research articles
Search
Showing results (191-200 of 321) with videos related to
Sort By:
Page
of 33
Cancers
|
December 11, 2022
Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer
Marina Muzza, Gabriele Pogliaghi, Carla Colombo, et al.
Frontiers in Endocrinology
|
July 28, 2022
Unilateral Surgery for Medullary Thyroid Carcinoma: Seeking for Clinical Practice Guidelines
Daqi Zhang, Carla Colombo, Hui Sun, et al.
European Thyroid Journal
|
July 4, 2024
2024 European Thyroid Association Guidelines on diagnosis and management of genetic disorders of thyroid hormone transport, metabolism and action
Luca Persani, Patrice Rodien, Carla Moran, et al.
European Thyroid Journal
|
April 24, 2024
Radiofrequency ablation is an effective treatment for Bethesda III thyroid nodules without genetic alterations
Laura Fugazzola, Maurilio Deandrea, Stefano Borgato, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
October 13, 2018
Effects of human recombinant type I IFNs (IFN-α2b and IFN-β1a) on growth and migration of primary endometrial stromal cells from women with deeply infiltrating endometriosis: A preliminary study
Alessandra Dicitore, Sara Castiglioni, Davide Saronni, et al.
Frontiers in Endocrinology
|
December 19, 2022
Genetic and phenotypic differences between sexes in congenital hypogonadotropic hypogonadism (CHH): Large cohort analysis from a single tertiary centre
Silvia Federici, Biagio Cangiano, Giovanni Goggi, 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.
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.
The Journal of Clinical Endocrinology and Metabolism
|
June 7, 2002
Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism
Luisella Alberti, Maria Carla Proverbio, Sabine Costagliola, et al.
BMC Medical Genetics
|
May 7, 2011
SNPs and real-time quantitative PCR method for constitutional allelic copy number determination, the VPREB1 marker case
Marcello Frigerio, Elena Passeri, Tiziana de Filippis, et al.
Page
of 33