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Journal of the Endocrine Society
|
March 2, 2019
Influence of Hashimoto Thyroiditis on the Development of Thyroid Nodules and Cancer in Children and Adolescents
Giorgio Radetti, Sandro Loche, Valeria D'Antonio, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2009
Reassessment of the growth hormone status in young adults with childhood-onset growth hormone deficiency: reappraisal of insulin tolerance testing
Andrea Secco, Natascia di Iorgi, Flavia Napoli, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 22, 2011
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome
Graziano Grugni, Antonino Crinò, Sara Pagani, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 9, 2006
Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure
Elisa Di Pasquale, Raffaella Rossetti, Anna Marozzi, et al.
Journal of Clinical Medicine
|
July 12, 2025
Assessing Metabolic Syndrome Risk in Children and Adolescents with Prader-Willi Syndrome: A Comparison of Index Performance
Graziano Grugni, Fiorenzo Lupi, Mirko Bonetti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2016
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects
Tiziana de Filippis, Federica Marelli, Gabriella Nebbia, et al.
Hormone Research in Paediatrics
|
June 19, 2026
Risk of Thyroid Cancer in Children, Adolescents and Young Adults with Hashimoto Thyroiditis: a 27 Years Follow-up Study
Giorgio Radetti, Fiorenzo Lupi, Sandro Loche, et al.
Human Molecular Genetics
|
April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidism
Tiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, 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 hyperthyrotropinemia
Davide Calebiro, Giulia Gelmini, Daniela Cordella, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 28, 2020
Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort
Donatella Capalbo, Cristina Moracas, Marco Cappa, et al.
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of 8
Search research articles
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Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
Journal of the Endocrine Society
|
March 2, 2019
Influence of Hashimoto Thyroiditis on the Development of Thyroid Nodules and Cancer in Children and Adolescents
Giorgio Radetti, Sandro Loche, Valeria D'Antonio, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2009
Reassessment of the growth hormone status in young adults with childhood-onset growth hormone deficiency: reappraisal of insulin tolerance testing
Andrea Secco, Natascia di Iorgi, Flavia Napoli, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 22, 2011
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome
Graziano Grugni, Antonino Crinò, Sara Pagani, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 9, 2006
Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure
Elisa Di Pasquale, Raffaella Rossetti, Anna Marozzi, et al.
Journal of Clinical Medicine
|
July 12, 2025
Assessing Metabolic Syndrome Risk in Children and Adolescents with Prader-Willi Syndrome: A Comparison of Index Performance
Graziano Grugni, Fiorenzo Lupi, Mirko Bonetti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2016
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects
Tiziana de Filippis, Federica Marelli, Gabriella Nebbia, et al.
Hormone Research in Paediatrics
|
June 19, 2026
Risk of Thyroid Cancer in Children, Adolescents and Young Adults with Hashimoto Thyroiditis: a 27 Years Follow-up Study
Giorgio Radetti, Fiorenzo Lupi, Sandro Loche, et al.
Human Molecular Genetics
|
April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidism
Tiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, 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 hyperthyrotropinemia
Davide Calebiro, Giulia Gelmini, Daniela Cordella, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 28, 2020
Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort
Donatella Capalbo, Cristina Moracas, Marco Cappa, et al.
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of 8