Showing results (61-70 of 232) with videos related to

Sort By:
Pageof 24
Endocrine|February 27, 2014
Overexpression of genes involved in miRNA biogenesis in medullary thyroid carcinomas with RET mutationCinzia Puppin, Cosimo Durante, Marialuisa Sponziello, et al.
Nature Clinical Practice. Endocrinology & Metabolism|August 25, 2006
Thyroid-hormone therapy and thyroid cancer: a reassessmentBernadette Biondi, Sebastiano Filetti, Martin Schlumberger
Endocrine|December 16, 2015
Papillary thyroid carcinomas with biochemical incomplete or indeterminate responses to initial treatment: repeat stimulated thyroglobulin assay to identify disease-free patientsLivia Lamartina, Teresa Montesano, Fabiana Trulli, et al.
Endocrine-Related Cancer|February 26, 2016
MCM5 as a target of BET inhibitors in thyroid cancer cellsCatia Mio, Elisa Lavarone, Ketty Conzatti, et al.
Thyroid : Official Journal of the American Thyroid Association|August 19, 2007
hNIS protein in thyroid: the iodine supply influences its expression and localizationAngela Scipioni, Elisabetta Ferretti, Giuseppe Soda, et al.
Thyroid : Official Journal of the American Thyroid Association|August 16, 2017
Temporal Changes in Thyroid Nodule Volume: Lack of Effect on Paranodular Thyroid Tissue VolumeGiorgio Grani, Rocco Bruno, Giuseppe Lucisano, et al.
Thyroid : Official Journal of the American Thyroid Association|April 11, 2008
Expression of hepatocyte nuclear factor-1alpha mRNA in human anaplastic thyroid cancer cell lines and tumorsJimin Xu, Sebastiano Filetti, Jerome M Hershman
The Journal of Clinical Endocrinology and Metabolism|December 13, 2007
Type 2 deiodinase polymorphism (threonine 92 alanine) predicts L-thyroxine dose to achieve target thyrotropin levels in thyroidectomized patientsMassimo Torlontano, Cosimo Durante, Isabella Torrente, et al.
Molecular and Cellular Endocrinology|March 15, 2017
Silencing of hTERT blocks growth and migration of anaplastic thyroid cancer cellsValentina Maggisano, Marilena Celano, Giovanni Enrico Lombardo, et al.
Clinical Endocrinology|September 6, 2012
A new germline VHL gene mutation in three patients with apparently sporadic pheochromocytomaAngela V D'Elia, Franco Grimaldi, Stefano Pizzolitto, et al.
Pageof 24