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Alessandro Salvatoni

Showing results (21-30 of 38) with videos related to

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European Journal of Endocrinology|December 19, 2009
Children with Prader-Willi syndrome exhibit more evident meal-induced responses in plasma ghrelin and peptide YY levels than obese and lean childrenCarla Bizzarri, Antonello E Rigamonti, Antonella Luce, et al.
Acta Diabetologica|June 23, 2017
Whole lipid profile and not only HDL cholesterol is impaired in children with coexisting type 1 diabetes and untreated celiac diseaseSilvana Salardi, Giulio Maltoni, Stefano Zucchini, et al.
Hormone Research in Paediatrics|May 9, 2013
Genetic analysis of Italian patients with congenital hyperinsulinism of infancyPaola Sogno Valin, Maria Carla Proverbio, Cecilia Diceglie, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2013
Growth hormone therapy and respiratory disorders: long-term follow-up in PWS childrenJenny Berini, Valeria Spica Russotto, Paolo Castelnuovo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2011
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndromeGraziano Grugni, Antonino Crinò, Sara Pagani, et al.
Journal of Diabetes and Its Complications|November 25, 2015
Ketoacidosis at diagnosis in childhood-onset diabetes and the risk of retinopathy 20years laterSilvana Salardi, Massimo Porta, Giulio Maltoni, et al.
Clinical Endocrinology|January 15, 2013
Central adrenal insufficiency in young adults with Prader-Willi syndromeGraziano Grugni, Luciano Beccaria, Andrea Corrias, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2019
Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patientsLorenzo Iughetti, Giulia Vivi, Antonio Balsamo, et al.
Diabetes, Obesity & Metabolism|May 17, 2021
Decreasing prevalence of retinopathy in childhood-onset type 1 diabetes over the last decade: A comparison of two cohorts diagnosed 10 years apartSilvana Salardi, Massimo Porta, Giulio Maltoni, et al.
Plos One|July 23, 2013
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinismMaria Carla Proverbio, Eleonora Mangano, Alessandra Gessi, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
European Journal of Endocrinology|December 19, 2009
Children with Prader-Willi syndrome exhibit more evident meal-induced responses in plasma ghrelin and peptide YY levels than obese and lean childrenCarla Bizzarri, Antonello E Rigamonti, Antonella Luce, et al.
Acta Diabetologica|June 23, 2017
Whole lipid profile and not only HDL cholesterol is impaired in children with coexisting type 1 diabetes and untreated celiac diseaseSilvana Salardi, Giulio Maltoni, Stefano Zucchini, et al.
Hormone Research in Paediatrics|May 9, 2013
Genetic analysis of Italian patients with congenital hyperinsulinism of infancyPaola Sogno Valin, Maria Carla Proverbio, Cecilia Diceglie, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2013
Growth hormone therapy and respiratory disorders: long-term follow-up in PWS childrenJenny Berini, Valeria Spica Russotto, Paolo Castelnuovo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2011
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndromeGraziano Grugni, Antonino Crinò, Sara Pagani, et al.
Journal of Diabetes and Its Complications|November 25, 2015
Ketoacidosis at diagnosis in childhood-onset diabetes and the risk of retinopathy 20years laterSilvana Salardi, Massimo Porta, Giulio Maltoni, et al.
Clinical Endocrinology|January 15, 2013
Central adrenal insufficiency in young adults with Prader-Willi syndromeGraziano Grugni, Luciano Beccaria, Andrea Corrias, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2019
Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patientsLorenzo Iughetti, Giulia Vivi, Antonio Balsamo, et al.
Diabetes, Obesity & Metabolism|May 17, 2021
Decreasing prevalence of retinopathy in childhood-onset type 1 diabetes over the last decade: A comparison of two cohorts diagnosed 10 years apartSilvana Salardi, Massimo Porta, Giulio Maltoni, et al.
Plos One|July 23, 2013
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinismMaria Carla Proverbio, Eleonora Mangano, Alessandra Gessi, et al.
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