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Fabrizio Barbetti

Showing results (31-40 of 88) with videos related to

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Diabetic Medicine : a Journal of the British Diabetic Association|August 19, 2023
A rare cause of transient neonatal diabetes mellitus: Spontaneous HNF1B splice variantGiulia Pezzino, Rosario Ruta, Novella Rapini, et al.
BMC Genetics|March 8, 2006
Search for genetic variants in the p66Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular diseaseFederica Sentinelli, Stefano Romeo, Fabrizio Barbetti, et al.
Frontiers in Endocrinology|May 30, 2023
Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variantsValentina Mancioppi, Erica Pozzi, Sara Zanetta, et al.
Plos One|May 14, 2013
Functional characterization of a novel KCNJ11 in frame mutation-deletion associated with infancy-onset diabetes and a mild form of intermediate DEND: a battle between K(ATP) gain of channel activity and loss of channel expressionYu-Wen Lin, Anlong Li, Valeria Grasso, et al.
Pediatric Diabetes|February 8, 2018
Severe insulin resistance in disguise: A familial case of reactive hypoglycemia associated with a novel heterozygous INSR mutationStefania Innaurato, Gemma V Brierley, Valeria Grasso, et al.
Diabetes Care|October 9, 2008
Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodiesRiccardo Bonfanti, Carlo Colombo, Valentina Nocerino, et al.
Hormone Research|October 28, 2008
Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian childrenClaudia Brufani, Armando Grossi, Danilo Fintini, et al.
Hormone Research in Paediatrics|June 19, 2013
IGF2 methylation is associated with lipid profile in obese childrenAnnalisa Deodati, Elena Inzaghi, Alice Liguori, et al.
Diabetes|February 24, 2012
Impaired cleavage of preproinsulin signal peptide linked to autosomal-dominant diabetesMing Liu, Roberto Lara-Lemus, Shu-ou Shan, et al.
Acta Diabetologica|August 5, 2015
Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatmentFederica Ortolani, Elvira Piccinno, Valeria Grasso, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Diabetic Medicine : a Journal of the British Diabetic Association|August 19, 2023
A rare cause of transient neonatal diabetes mellitus: Spontaneous HNF1B splice variantGiulia Pezzino, Rosario Ruta, Novella Rapini, et al.
BMC Genetics|March 8, 2006
Search for genetic variants in the p66Shc longevity gene by PCR-single strand conformational polymorphism in patients with early-onset cardiovascular diseaseFederica Sentinelli, Stefano Romeo, Fabrizio Barbetti, et al.
Frontiers in Endocrinology|May 30, 2023
Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variantsValentina Mancioppi, Erica Pozzi, Sara Zanetta, et al.
Plos One|May 14, 2013
Functional characterization of a novel KCNJ11 in frame mutation-deletion associated with infancy-onset diabetes and a mild form of intermediate DEND: a battle between K(ATP) gain of channel activity and loss of channel expressionYu-Wen Lin, Anlong Li, Valeria Grasso, et al.
Pediatric Diabetes|February 8, 2018
Severe insulin resistance in disguise: A familial case of reactive hypoglycemia associated with a novel heterozygous INSR mutationStefania Innaurato, Gemma V Brierley, Valeria Grasso, et al.
Diabetes Care|October 9, 2008
Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodiesRiccardo Bonfanti, Carlo Colombo, Valentina Nocerino, et al.
Hormone Research|October 28, 2008
Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian childrenClaudia Brufani, Armando Grossi, Danilo Fintini, et al.
Hormone Research in Paediatrics|June 19, 2013
IGF2 methylation is associated with lipid profile in obese childrenAnnalisa Deodati, Elena Inzaghi, Alice Liguori, et al.
Diabetes|February 24, 2012
Impaired cleavage of preproinsulin signal peptide linked to autosomal-dominant diabetesMing Liu, Roberto Lara-Lemus, Shu-ou Shan, et al.
Acta Diabetologica|August 5, 2015
Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatmentFederica Ortolani, Elvira Piccinno, Valeria Grasso, et al.
Pageof 9