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Marco Cappa

Showing results (131-140 of 207) with videos related to

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Journal of Endocrinological Investigation|April 15, 2025
Diagnostic cut-offs of 17-hydroxyprogesterone by LC-MS/MS in children with non-classical congenital adrenal hyperplasiaCarla Bizzarri, Laura Chioma, Giorgia Bottaro, et al.
Clinical Genetics|March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short statureAlessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Pediatric Obesity|February 10, 2022
Prevalence of prediabetes in children and adolescents by class of obesityStefania Pedicelli, Danilo Fintini, Lucilla Ravà, et al.
International Journal of Molecular Sciences|December 9, 2023
Low Levels of Serum Total Vitamin B12 Are Associated with Worse Metabolic Phenotype in a Large Population of Children, Adolescents and Young Adults, from Underweight to Severe ObesityAlessia Aureli, Rosanna Recupero, Michela Mariani, et al.
Hormone Research in Paediatrics|July 4, 2024
Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre StudyMarco Cappa, Francesco d'Aniello, Maria Cristina Digilio, et al.
Archives of Disease in Childhood|August 25, 2011
Thyroid autoimmunity in children with coeliac disease: a prospective surveyAntonella Diamanti, Francesca Ferretti, Rinaldo Guglielmi, et al.
International Journal of Molecular Sciences|October 26, 2024
The Putative Role of <i>TIM-3</i> Variants in Polyendocrine Autoimmunity: Insights from a WES InvestigationAndrea Ariolli, Emanuele Agolini, Tommaso Mazza, et al.
Clinical Endocrinology|October 11, 2011
The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-upGiorgio Radetti, Mara Maselli, Fabio Buzi, et al.
Diabetes Care|September 1, 2010
No protective effect of calcitriol on beta-cell function in recent-onset type 1 diabetes: the IMDIAB XIII trialCarla Bizzarri, Dario Pitocco, Nicola Napoli, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2004
Parental origin of Gsalpha mutations in the McCune-Albright syndrome and in isolated endocrine tumorsGiovanna Mantovani, Sara Bondioni, Andrea G Lania, et al.
Pageof 21

Showing results (131-140 of 207) with videos related to

Sort By:
Pageof 21
Journal of Endocrinological Investigation|April 15, 2025
Diagnostic cut-offs of 17-hydroxyprogesterone by LC-MS/MS in children with non-classical congenital adrenal hyperplasiaCarla Bizzarri, Laura Chioma, Giorgia Bottaro, et al.
Clinical Genetics|March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short statureAlessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Pediatric Obesity|February 10, 2022
Prevalence of prediabetes in children and adolescents by class of obesityStefania Pedicelli, Danilo Fintini, Lucilla Ravà, et al.
International Journal of Molecular Sciences|December 9, 2023
Low Levels of Serum Total Vitamin B12 Are Associated with Worse Metabolic Phenotype in a Large Population of Children, Adolescents and Young Adults, from Underweight to Severe ObesityAlessia Aureli, Rosanna Recupero, Michela Mariani, et al.
Hormone Research in Paediatrics|July 4, 2024
Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre StudyMarco Cappa, Francesco d'Aniello, Maria Cristina Digilio, et al.
Archives of Disease in Childhood|August 25, 2011
Thyroid autoimmunity in children with coeliac disease: a prospective surveyAntonella Diamanti, Francesca Ferretti, Rinaldo Guglielmi, et al.
International Journal of Molecular Sciences|October 26, 2024
The Putative Role of <i>TIM-3</i> Variants in Polyendocrine Autoimmunity: Insights from a WES InvestigationAndrea Ariolli, Emanuele Agolini, Tommaso Mazza, et al.
Clinical Endocrinology|October 11, 2011
The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-upGiorgio Radetti, Mara Maselli, Fabio Buzi, et al.
Diabetes Care|September 1, 2010
No protective effect of calcitriol on beta-cell function in recent-onset type 1 diabetes: the IMDIAB XIII trialCarla Bizzarri, Dario Pitocco, Nicola Napoli, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2004
Parental origin of Gsalpha mutations in the McCune-Albright syndrome and in isolated endocrine tumorsGiovanna Mantovani, Sara Bondioni, Andrea G Lania, et al.
Pageof 21