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Showing results (51-60 of 207) with videos related to

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Hormone Research in Paediatrics|August 1, 2013
Systematic review of metformin use in obese nondiabetic children and adolescentsClaudia Brufani, Antonino Crinò, Danilo Fintini, et al.
Pediatric Diabetes|March 4, 2011
Use of metformin in pediatric ageClaudia Brufani, Danilo Fintini, Valerio Nobili, et al.
Hormone Research in Paediatrics|September 23, 2015
Brain Magnetic Resonance Imaging as First-Line Investigation for Growth Hormone Deficiency Diagnosis in Early ChildhoodValentina Pampanini, Stefania Pedicelli, Jessica Gubinelli, et al.
Gene|December 25, 2012
Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10pArmando Grossi, Alessia Palma, Ginevra Zanni, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 29, 2013
ZnT8 antibodies in patients with cystic fibrosis: an expression of secondary beta-cell damage?Carla Bizzarri, Germana Giannone, Danila Benevento, et al.
Frontiers in Endocrinology|March 17, 2023
COVID-19 pandemic phases and female precocious puberty: The experience of the past 4 years (2019 through 2022) in an Italian tertiary centerLaura Chioma, Mariangela Chiarito, Giorgia Bottaro, et al.
Endocrinology, Diabetes & Metabolism Case Reports|May 20, 2021
ABCD1 gene mutation in an Italian family with X-linkedadrenoleukodystrophy: case seriesAngelika Mohn, Nella Polidori, Chiara Aiello, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarcheCarla Bizzarri, Francesca Crea, Romana Marini, et al.
Clinical Endocrinology|December 11, 2012
Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoringPaola Cambiaso, Riccardo Schiaffini, Giuseppe Pontrelli, et al.
Italian Journal of Pediatrics|August 4, 2016
Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experienceCarla Bizzarri, Nicole Olivini, Stefania Pedicelli, et al.
Pageof 21

Showing results (51-60 of 207) with videos related to

Sort By:
Pageof 21
Hormone Research in Paediatrics|August 1, 2013
Systematic review of metformin use in obese nondiabetic children and adolescentsClaudia Brufani, Antonino Crinò, Danilo Fintini, et al.
Pediatric Diabetes|March 4, 2011
Use of metformin in pediatric ageClaudia Brufani, Danilo Fintini, Valerio Nobili, et al.
Hormone Research in Paediatrics|September 23, 2015
Brain Magnetic Resonance Imaging as First-Line Investigation for Growth Hormone Deficiency Diagnosis in Early ChildhoodValentina Pampanini, Stefania Pedicelli, Jessica Gubinelli, et al.
Gene|December 25, 2012
Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10pArmando Grossi, Alessia Palma, Ginevra Zanni, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 29, 2013
ZnT8 antibodies in patients with cystic fibrosis: an expression of secondary beta-cell damage?Carla Bizzarri, Germana Giannone, Danila Benevento, et al.
Frontiers in Endocrinology|March 17, 2023
COVID-19 pandemic phases and female precocious puberty: The experience of the past 4 years (2019 through 2022) in an Italian tertiary centerLaura Chioma, Mariangela Chiarito, Giorgia Bottaro, et al.
Endocrinology, Diabetes & Metabolism Case Reports|May 20, 2021
ABCD1 gene mutation in an Italian family with X-linkedadrenoleukodystrophy: case seriesAngelika Mohn, Nella Polidori, Chiara Aiello, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarcheCarla Bizzarri, Francesca Crea, Romana Marini, et al.
Clinical Endocrinology|December 11, 2012
Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoringPaola Cambiaso, Riccardo Schiaffini, Giuseppe Pontrelli, et al.
Italian Journal of Pediatrics|August 4, 2016
Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experienceCarla Bizzarri, Nicole Olivini, Stefania Pedicelli, et al.
Pageof 21