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Fabrizio Barbetti

Showing results (61-70 of 88) with videos related to

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Pediatric Diabetes|June 15, 2012
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutationDomenica Battaglia, Yu-Wen Lin, Claudia Brogna, et al.
Diabetes|March 28, 2002
The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapyHenrik B T Christesen, Bendt B Jacobsen, Stella Odili, et al.
Hormone Research in Paediatrics|April 4, 2024
A New Variant in the GATA6 Gene Associated with Tracheoesophageal Fistula, Pulmonary Vein Stenosis, and Neonatal DiabetesFlaminia Pugnaloni, Ludovica Martini, Domenico Umberto De Rose, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 3, 2002
Role of transglutaminase 2 in glucose tolerance: knockout mice studies and a putative mutation in a MODY patientFrancesca Bernassola, Massimo Federici, Marco Corazzari, et al.
Plos One|November 19, 2013
Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF)Michele Pinelli, Fabio Acquaviva, Fabrizio Barbetti, et al.
Acta Diabetologica|September 30, 2022
Monogenic diabetes clinic (MDC): 3-year experienceNovella Rapini, Patrizia I Patera, Riccardo Schiaffini, et al.
Acta Diabetologica|November 5, 2022
Correction to: Monogenic diabetes clinic (MDC): 3‑year experienceNovella Rapini, Patrizia I Patera, Riccardo Schiaffini, et al.
BMC Medical Genetics|March 16, 2010
Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)Trine W Boesgaard, Stepanka Pruhova, Ehm A Andersson, et al.
Diabetes|October 29, 2010
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical managementKaren J Loechner, Alejandro Akrouh, Harley T Kurata, et al.
Clinical Endocrinology|January 4, 2014
Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screeningArianna Maiorana, Fabrizio Barbetti, Arianna Boiani, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Pediatric Diabetes|June 15, 2012
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutationDomenica Battaglia, Yu-Wen Lin, Claudia Brogna, et al.
Diabetes|March 28, 2002
The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapyHenrik B T Christesen, Bendt B Jacobsen, Stella Odili, et al.
Hormone Research in Paediatrics|April 4, 2024
A New Variant in the GATA6 Gene Associated with Tracheoesophageal Fistula, Pulmonary Vein Stenosis, and Neonatal DiabetesFlaminia Pugnaloni, Ludovica Martini, Domenico Umberto De Rose, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 3, 2002
Role of transglutaminase 2 in glucose tolerance: knockout mice studies and a putative mutation in a MODY patientFrancesca Bernassola, Massimo Federici, Marco Corazzari, et al.
Plos One|November 19, 2013
Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF)Michele Pinelli, Fabio Acquaviva, Fabrizio Barbetti, et al.
Acta Diabetologica|September 30, 2022
Monogenic diabetes clinic (MDC): 3-year experienceNovella Rapini, Patrizia I Patera, Riccardo Schiaffini, et al.
Acta Diabetologica|November 5, 2022
Correction to: Monogenic diabetes clinic (MDC): 3‑year experienceNovella Rapini, Patrizia I Patera, Riccardo Schiaffini, et al.
BMC Medical Genetics|March 16, 2010
Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)Trine W Boesgaard, Stepanka Pruhova, Ehm A Andersson, et al.
Diabetes|October 29, 2010
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical managementKaren J Loechner, Alejandro Akrouh, Harley T Kurata, et al.
Clinical Endocrinology|January 4, 2014
Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screeningArianna Maiorana, Fabrizio Barbetti, Arianna Boiani, et al.
Pageof 9