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E Macchia

Showing results (81-90 of 94) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alphaP E Macchia, Y Takeuchi, T Kawai, et al.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
Thyroid : Official Journal of the American Thyroid Association|March 7, 2009
Thyroid nodules and related symptoms are stably controlled two years after radiofrequency thermal ablationStefano Spiezia, Roberto Garberoglio, Francesco Milone, et al.
Journal of the American Geriatrics Society|September 5, 2007
Efficacy and safety of radiofrequency thermal ablation in the treatment of thyroid nodules with pressure symptoms in elderly patientsStefano Spiezia, Roberto Garberoglio, Carolina Di Somma, et al.
Nature Genetics|August 11, 1998
A mouse model for hereditary thyroid dysgenesis and cleft palateM De Felice, C Ovitt, E Biffali, et al.
The Journal of Clinical Endocrinology and Metabolism|September 29, 2012
Thyroid nodules treated with percutaneous radiofrequency thermal ablation: a comparative studyA Faggiano, V Ramundo, A P Assanti, et al.
Biofactors (Oxford, England)|March 3, 2017
Selenium supplementation modulates apoptotic processes in thyroid follicular cellsImmacolata C Nettore, Emma De Nisco, Silvio Desiderio, et al.
Journal of Endocrinological Investigation|November 10, 2010
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.
Development (Cambridge, England)|May 9, 1998
Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LHD Acampora, S Mazan, F Tuorto, et al.
Nature Genetics|May 20, 1998
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisP E Macchia, P Lapi, H Krude, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Increased sensitivity to thyroid hormone in mice with complete deficiency of thyroid hormone receptor alphaP E Macchia, Y Takeuchi, T Kawai, et al.
Journal of Endocrinological Investigation|June 23, 2009
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.
Thyroid : Official Journal of the American Thyroid Association|March 7, 2009
Thyroid nodules and related symptoms are stably controlled two years after radiofrequency thermal ablationStefano Spiezia, Roberto Garberoglio, Francesco Milone, et al.
Journal of the American Geriatrics Society|September 5, 2007
Efficacy and safety of radiofrequency thermal ablation in the treatment of thyroid nodules with pressure symptoms in elderly patientsStefano Spiezia, Roberto Garberoglio, Carolina Di Somma, et al.
Nature Genetics|August 11, 1998
A mouse model for hereditary thyroid dysgenesis and cleft palateM De Felice, C Ovitt, E Biffali, et al.
The Journal of Clinical Endocrinology and Metabolism|September 29, 2012
Thyroid nodules treated with percutaneous radiofrequency thermal ablation: a comparative studyA Faggiano, V Ramundo, A P Assanti, et al.
Biofactors (Oxford, England)|March 3, 2017
Selenium supplementation modulates apoptotic processes in thyroid follicular cellsImmacolata C Nettore, Emma De Nisco, Silvio Desiderio, et al.
Journal of Endocrinological Investigation|November 10, 2010
Screening for mutations in the ISL1 gene in patients with thyroid dysgenesisA M Ferrara, G Rossi, E Zampella, et al.
Development (Cambridge, England)|May 9, 1998
Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LHD Acampora, S Mazan, F Tuorto, et al.
Nature Genetics|May 20, 1998
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisP E Macchia, P Lapi, H Krude, et al.
Pageof 10