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Luca Persani

Showing results (281-290 of 321) with videos related to

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Annals of the New York Academy of Sciences|October 4, 2007
X monosomy in female systemic lupus erythematosusPietro Invernizzi, Monica Miozzo, Sabine Oertelt-Prigione, et al.
The Journal of Clinical Endocrinology and Metabolism|February 21, 2014
Refining calcium test for the diagnosis of medullary thyroid cancer: cutoffs, procedures, and safetyCaterina Mian, Michela Perrino, Carla Colombo, et al.
European Journal of Endocrinology|May 26, 2023
Towards an individualized management of pubertal induction in girls with hypogonadism: insight into the best replacement outcomes from a large multicentre registryGiulia Rodari, Silvia Federici, Tommaso Todisco, et al.
The Journal of Clinical Endocrinology and Metabolism|December 31, 2020
Procoagulant Imbalance in Klinefelter Syndrome Assessed by Thrombin Generation Assay and Whole-Blood ThromboelastometryRita Indirli, Emanuele Ferrante, Erica Scalambrino, et al.
Human Molecular Genetics|April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidismTiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2019
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn From Discordant Twins?Emanuela Medda, Maria Cristina Vigone, Alessandra Cassio, et al.
Endocrine|January 31, 2016
Bone turnover and mineral density in adult thalassemic patients: relationships with growth hormone secretory status and circulating somatomedinsMassimo Scacchi, Leila Danesi, Agnese Cattaneo, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2011
Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemiaDavide Calebiro, Giulia Gelmini, Daniela Cordella, et al.
Thyroid : Official Journal of the American Thyroid Association|March 5, 2014
Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolismSamuel Refetoff, J H Duncan Bassett, Paolo Beck-Peccoz, et al.
International Journal of Environmental Research and Public Health|December 1, 2020
The EuRRECa Project as a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical OutcomesSalma R Ali, Jillian Bryce, Li En Tan, et al.
Pageof 33

Showing results (281-290 of 321) with videos related to

Sort By:
Pageof 33
Annals of the New York Academy of Sciences|October 4, 2007
X monosomy in female systemic lupus erythematosusPietro Invernizzi, Monica Miozzo, Sabine Oertelt-Prigione, et al.
The Journal of Clinical Endocrinology and Metabolism|February 21, 2014
Refining calcium test for the diagnosis of medullary thyroid cancer: cutoffs, procedures, and safetyCaterina Mian, Michela Perrino, Carla Colombo, et al.
European Journal of Endocrinology|May 26, 2023
Towards an individualized management of pubertal induction in girls with hypogonadism: insight into the best replacement outcomes from a large multicentre registryGiulia Rodari, Silvia Federici, Tommaso Todisco, et al.
The Journal of Clinical Endocrinology and Metabolism|December 31, 2020
Procoagulant Imbalance in Klinefelter Syndrome Assessed by Thrombin Generation Assay and Whole-Blood ThromboelastometryRita Indirli, Emanuele Ferrante, Erica Scalambrino, et al.
Human Molecular Genetics|April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidismTiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2019
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn From Discordant Twins?Emanuela Medda, Maria Cristina Vigone, Alessandra Cassio, et al.
Endocrine|January 31, 2016
Bone turnover and mineral density in adult thalassemic patients: relationships with growth hormone secretory status and circulating somatomedinsMassimo Scacchi, Leila Danesi, Agnese Cattaneo, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2011
Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemiaDavide Calebiro, Giulia Gelmini, Daniela Cordella, et al.
Thyroid : Official Journal of the American Thyroid Association|March 5, 2014
Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolismSamuel Refetoff, J H Duncan Bassett, Paolo Beck-Peccoz, et al.
International Journal of Environmental Research and Public Health|December 1, 2020
The EuRRECa Project as a Model for Data Access and Governance Policies for Rare Disease Registries That Collect Clinical OutcomesSalma R Ali, Jillian Bryce, Li En Tan, et al.
Pageof 33