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Luca Persani

Showing results (211-220 of 321) with videos related to

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European Thyroid Journal|October 31, 2018
2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central HypothyroidismLuca Persani, Georg Brabant, Mehul Dattani, et al.
Frontiers in Endocrinology|July 25, 2024
Exploring the multifaceted antitumor activity of axitinib in lung carcinoidsMonica Oldani, Maria Celeste Cantone, Germano Gaudenzi, et al.
Journal of Endocrinological Investigation|June 16, 2020
Central hypogonadism in Klinefelter syndrome: report of two cases and review of the literatureBiagio Cangiano, Rita Indirli, Eriselda Profka, et al.
Orphanet Journal of Rare Diseases|April 19, 2015
The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studiesCarla Colombo, Emanuela Minna, Maria Grazia Rizzetti, et al.
International Journal of Molecular Sciences|April 3, 2021
Vandetanib versus Cabozantinib in Medullary Thyroid Carcinoma: A Focus on Anti-Angiogenic Effects in Zebrafish ModelSilvia Carra, Germano Gaudenzi, Alessandra Dicitore, et al.
Clinical Endocrinology|June 1, 2017
Mild TSH resistance: Clinical and hormonal features in childhood and adulthoodMaria Cristina Vigone, Marianna Di Frenna, Fabiana Guizzardi, et al.
Cancers|September 23, 2022
Preclinical Evaluation of Novel Tyrosine-Kinase Inhibitors in Medullary Thyroid CancerDavide Saronni, Germano Gaudenzi, Alessandra Dicitore, et al.
Molecular and Cellular Endocrinology|January 31, 2012
Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing lossValentina Cirello, Claudia Bazzini, Valeria Vezzoli, et al.
Plos One|April 6, 2021
The relationship between liver histology and thyroid function tests in patients with non-alcoholic fatty liver disease (NAFLD)Roberta D'Ambrosio, Irene Campi, Marco Maggioni, et al.
Plos Genetics|May 3, 2013
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheepJulie Demars, Stéphane Fabre, Julien Sarry, et al.
Pageof 33

Showing results (211-220 of 321) with videos related to

Sort By:
Pageof 33
European Thyroid Journal|October 31, 2018
2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central HypothyroidismLuca Persani, Georg Brabant, Mehul Dattani, et al.
Frontiers in Endocrinology|July 25, 2024
Exploring the multifaceted antitumor activity of axitinib in lung carcinoidsMonica Oldani, Maria Celeste Cantone, Germano Gaudenzi, et al.
Journal of Endocrinological Investigation|June 16, 2020
Central hypogonadism in Klinefelter syndrome: report of two cases and review of the literatureBiagio Cangiano, Rita Indirli, Eriselda Profka, et al.
Orphanet Journal of Rare Diseases|April 19, 2015
The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studiesCarla Colombo, Emanuela Minna, Maria Grazia Rizzetti, et al.
International Journal of Molecular Sciences|April 3, 2021
Vandetanib versus Cabozantinib in Medullary Thyroid Carcinoma: A Focus on Anti-Angiogenic Effects in Zebrafish ModelSilvia Carra, Germano Gaudenzi, Alessandra Dicitore, et al.
Clinical Endocrinology|June 1, 2017
Mild TSH resistance: Clinical and hormonal features in childhood and adulthoodMaria Cristina Vigone, Marianna Di Frenna, Fabiana Guizzardi, et al.
Cancers|September 23, 2022
Preclinical Evaluation of Novel Tyrosine-Kinase Inhibitors in Medullary Thyroid CancerDavide Saronni, Germano Gaudenzi, Alessandra Dicitore, et al.
Molecular and Cellular Endocrinology|January 31, 2012
Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing lossValentina Cirello, Claudia Bazzini, Valeria Vezzoli, et al.
Plos One|April 6, 2021
The relationship between liver histology and thyroid function tests in patients with non-alcoholic fatty liver disease (NAFLD)Roberta D'Ambrosio, Irene Campi, Marco Maggioni, et al.
Plos Genetics|May 3, 2013
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheepJulie Demars, Stéphane Fabre, Julien Sarry, et al.
Pageof 33