about
Prevalence of type 1 diabetes autoantibodies (GADA, IA2, and IAA) in overweight and obese childrenAltered glucose homeostasis is associated with increased serum apelin levels in type 2 diabetes mellitus.Glycated hemoglobin for the diagnosis of diabetes and prediabetes: Diagnostic impact on obese and lean subjects, and phenotypic characterization.Lack of effect of apolipoprotein C3 polymorphisms on indices of liver steatosis, lipid profile and insulin resistance in obese Southern Europeans.Association of FTO polymorphisms with early age of obesity in obese Italian subjectsVGF Peptide Profiles in Type 2 Diabetic Patients' Plasma and in Obese Mice.The COBLL1 C allele is associated with lower serum insulin levels and lower insulin resistance in overweight and obese childrenAssociation of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis.High normal post-load plasma glucose, cardiometabolic risk factors and signs of organ damage in obese children.The vitamin D receptor functional variant rs2228570 (C>T) does not associate with type 2 diabetes mellitus.The Arg282Ser missense mutation in APOA5 gene determines a reduction of triglyceride and LDL-cholesterol in children, together with low serum levels of apolipoprotein A-V.Clinical application of best practice guidelines for the genetic diagnosis of MODY2 and MODY3.The 148M allele of the PNPLA3 gene is associated with indices of liver damage early in life.Oral glucose tolerance test in Italian overweight/obese children and adolescents results in a very high prevalence of impaired fasting glycaemia, but not of diabetes.High prevalence of diabetes-specific autoimmunity in first-degree relatives of Sardinian patients with type 1 diabetes.Presence of diabetes-specific autoimmunity in women with gestational diabetes mellitus (GDM) predicts impaired glucose regulation at follow-up.Search for Genetic Variant in the Apelin Gene by Resequencing and Association Study in European Subjects.The vitamin D receptor (VDR) gene rs11568820 variant is associated with type 2 diabetes and impaired insulin secretion in Italian adult subjects, and associates with increased cardio-metabolic risk in children.The perilipin 2 (PLIN2) gene Ser251Pro missense mutation is associated with reduced insulin secretion and increased insulin sensitivity in Italian obese subjects.Assessment of Adiponectin and Leptin as Biomarkers of Positive Metabolic Outcomes after Lifestyle Intervention in Overweight and Obese ChildrenTesting for type 1 diabetes autoantibodies in gestational diabetes mellitus (GDM): is it clinically useful?Prevalence of Type 1 diabetes autoantibodies (GAD and IA2) in Sardinian children and adolescents with autoimmune thyroiditisTransmembrane-6 superfamily member 2 (TM6SF2) E167K variant increases susceptibility to hepatic steatosis in obese children
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Michela Incani
@ast
Michela Incani
@en
Michela Incani
@es
Michela Incani
@nl
type
label
Michela Incani
@ast
Michela Incani
@en
Michela Incani
@es
Michela Incani
@nl
prefLabel
Michela Incani
@ast
Michela Incani
@en
Michela Incani
@es
Michela Incani
@nl
P106
P1153
24537382100
P31
P496
0000-0003-1623-5376