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Fabrizio Barbetti

Showing results (21-30 of 88) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 13, 2007
The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapyJoseph C Koster, Francesco Cadario, Cinzia Peruzzi, et al.
Minerva Pediatrics|July 21, 2021
Type 2 diabetes in pediatricsElena Fornari, Fabrizio Barbetti, Dario Iafusco, et al.
Pediatric Diabetes|May 23, 2009
Glucose tolerance status in 510 children and adolescents attending an obesity clinic in Central ItalyClaudia Brufani, Paolo Ciampalini, Armando Grossi, et al.
Molecular Biology Reports|June 14, 2024
Potential pathogenetic role of a novel ABCC8 missense variant on both transient neonatal diabetes mellitus and fetal growth restriction: a case reportAlessandro Perri, Simona Fattore, Angelo Minucci, et al.
Diabetes|January 30, 2007
An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of developmental delay, epilepsy, and neonatal diabetesRicard Masia, Joseph C Koster, Stefano Tumini, et al.
Diabetes Research and Clinical Practice|May 21, 2017
Insulin therapy in neonatal diabetes mellitus: a review of the literatureIvana Rabbone, Fabrizio Barbetti, Raffaella Gentilella, et al.
Diabetes Research and Clinical Practice|February 5, 2015
Survey on etiological diagnosis of diabetes in 1244 Italian diabetic children and adolescents: impact of access to genetic testingEnza Mozzillo, Giuseppina Salzano, Fabrizio Barbetti, et al.
Acta Diabetologica|April 17, 2025
DKA in a toddler negative to type 1 diabetes autoantibodies: unusual presentation of Kearn-Sayre syndromeAnnalisa Deodati, Novella Rapini, Diego Martinelli, et al.
Hormone Research in Paediatrics|December 16, 2025
Composite digenic diabetes linked to heterozygous variants of GCK and NEUROD1 - A Case ReportNovella Rapini, Claudia Brufani, Annalisa Deodati, et al.
Orphanet Journal of Rare Diseases|September 25, 2015
Ketogenic diet in a patient with congenital hyperinsulinism: a novel approach to prevent brain damageArianna Maiorana, Lucilla Manganozzi, Fabrizio Barbetti, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Endocrinology and Metabolism|December 13, 2007
The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapyJoseph C Koster, Francesco Cadario, Cinzia Peruzzi, et al.
Minerva Pediatrics|July 21, 2021
Type 2 diabetes in pediatricsElena Fornari, Fabrizio Barbetti, Dario Iafusco, et al.
Pediatric Diabetes|May 23, 2009
Glucose tolerance status in 510 children and adolescents attending an obesity clinic in Central ItalyClaudia Brufani, Paolo Ciampalini, Armando Grossi, et al.
Molecular Biology Reports|June 14, 2024
Potential pathogenetic role of a novel ABCC8 missense variant on both transient neonatal diabetes mellitus and fetal growth restriction: a case reportAlessandro Perri, Simona Fattore, Angelo Minucci, et al.
Diabetes|January 30, 2007
An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of developmental delay, epilepsy, and neonatal diabetesRicard Masia, Joseph C Koster, Stefano Tumini, et al.
Diabetes Research and Clinical Practice|May 21, 2017
Insulin therapy in neonatal diabetes mellitus: a review of the literatureIvana Rabbone, Fabrizio Barbetti, Raffaella Gentilella, et al.
Diabetes Research and Clinical Practice|February 5, 2015
Survey on etiological diagnosis of diabetes in 1244 Italian diabetic children and adolescents: impact of access to genetic testingEnza Mozzillo, Giuseppina Salzano, Fabrizio Barbetti, et al.
Acta Diabetologica|April 17, 2025
DKA in a toddler negative to type 1 diabetes autoantibodies: unusual presentation of Kearn-Sayre syndromeAnnalisa Deodati, Novella Rapini, Diego Martinelli, et al.
Hormone Research in Paediatrics|December 16, 2025
Composite digenic diabetes linked to heterozygous variants of GCK and NEUROD1 - A Case ReportNovella Rapini, Claudia Brufani, Annalisa Deodati, et al.
Orphanet Journal of Rare Diseases|September 25, 2015
Ketogenic diet in a patient with congenital hyperinsulinism: a novel approach to prevent brain damageArianna Maiorana, Lucilla Manganozzi, Fabrizio Barbetti, et al.
Pageof 9