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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 variant
Giulia 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 disease
Federica 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 variants
Valentina 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 expression
Yu-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 mutation
Stefania 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 autoantibodies
Riccardo Bonfanti, Carlo Colombo, Valentina Nocerino, et al.
Hormone Research
|
October 28, 2008
Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian children
Claudia Brufani, Armando Grossi, Danilo Fintini, et al.
Hormone Research in Paediatrics
|
June 19, 2013
IGF2 methylation is associated with lipid profile in obese children
Annalisa Deodati, Elena Inzaghi, Alice Liguori, et al.
Diabetes
|
February 24, 2012
Impaired cleavage of preproinsulin signal peptide linked to autosomal-dominant diabetes
Ming 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 treatment
Federica Ortolani, Elvira Piccinno, Valeria Grasso, et al.
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of 9
Search research articles
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Showing results (31-40 of 88) with videos related to
Sort By:
Page
of 9
Diabetic Medicine : a Journal of the British Diabetic Association
|
August 19, 2023
A rare cause of transient neonatal diabetes mellitus: Spontaneous HNF1B splice variant
Giulia 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 disease
Federica 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 variants
Valentina 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 expression
Yu-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 mutation
Stefania 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 autoantibodies
Riccardo Bonfanti, Carlo Colombo, Valentina Nocerino, et al.
Hormone Research
|
October 28, 2008
Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian children
Claudia Brufani, Armando Grossi, Danilo Fintini, et al.
Hormone Research in Paediatrics
|
June 19, 2013
IGF2 methylation is associated with lipid profile in obese children
Annalisa Deodati, Elena Inzaghi, Alice Liguori, et al.
Diabetes
|
February 24, 2012
Impaired cleavage of preproinsulin signal peptide linked to autosomal-dominant diabetes
Ming 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 treatment
Federica Ortolani, Elvira Piccinno, Valeria Grasso, et al.
Page
of 9