293 results on '"Prudente, Sabrina"'
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2. Recommendations for recognizing, risk stratifying, treating, and managing children and adolescents with hypoglycemia
3. The Arg1379His mutation in ABCC8 causes monogenic diabetes with variable phenotype presentation and incomplete penetrance
4. Contribution of rare variants in monogenic diabetes-genes to early-onset type 2 diabetes
5. Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients
6. Pathogenic variants of MODY-genes in adult patients with early-onset type 2 diabetes
7. Disentangling the heterogeneity of adulthood-onset non-autoimmune diabetes: a little closer but lot more to do
8. The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy
9. Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing
10. Validation in type 2 diabetes of a metabolomic signature of all‐cause mortality
11. A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients
12. Validation in type 2 diabetes of a metabolomic signature of all‐cause mortality.
13. Association of osteocalcin, osteoprotegerin and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes
14. Infrequent TRIB3 coding variants and coronary artery disease in type 2 diabetes
15. Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes
16. The PPARγ2 P12A polymorphism is not associated with all-cause mortality in patients with type 2 diabetes mellitus
17. Joint effect of insulin signaling genes on cardiovascular events and on whole body and endothelial insulin resistance
18. The rs12917707 polymorphism at the UMOD locus and glomerular filtration rate in individuals with type 2 diabetes: evidence of heterogeneity across two different European populations
19. The SH2B1 obesity locus is associated with myocardial infarction in diabetic patients and with NO synthase activity in endothelial cells
20. Supplemental Material
21. Deep Resequencing of 9 Candidate Genes Identifies a Role for ARAP1 and IGF2BP2 in Modulating Insulin Secretion Adjusted for Insulin Resistance in Obese Southern Europeans
22. Genetic Variant at the GLUL Locus Predicts All-Cause Mortality in Patients With Type 2 Diabetes
23. Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia
24. IRS1 G972R Missense Polymorphism Is Associated With Failure to Oral Antidiabetes Drugs in White Patients With Type 2 Diabetes From Italy
25. The emerging role of TRIB3 as a gene affecting human insulin resistance and related clinical outcomes
26. The allelic variant of LAR gene promoter –127 bp T→A is associated with reduced risk of obesity and other features related to insulin resistance
27. The allelic variant of LAR gene promoter --127 bp T[right arrow]A is associated with reduced risk of obesity and other features related to insulin resistance
28. The IRS1 G972R polymorphism and glomerular filtration rate in patients with type 2 diabetes of European ancestry
29. Association Between a Genetic Variant Related to Glutamic Acid Metabolism and Coronary Heart Disease in Individuals With Type 2 Diabetes
30. Joint Effect of Insulin Signaling Genes on Insulin Secretion and Glucose Homeostasis
31. The 9p21 coronary artery disease locus and kidney dysfunction in patients with Type 2 diabetes mellitus
32. The Mammalian Tribbles Homolog TRIB3, Glucose Homeostasis, and Cardiovascular Diseases
33. PPARγ2 P12A polymorphism and albuminuria in patients with type 2 diabetes: a meta-analysis of case–control studies
34. The ENPP1 Q121 Variant Predicts Major Cardiovascular Events in High-Risk Individuals: Evidence for Interaction With Obesity in Diabetic Patients
35. The TRIB3 R84 variant is associated with increased carotid intima–media thickness in vivo and with enhanced MAPK signalling in human endothelial cells
36. Association of the 1q25 diabetes-specific coronary heart disease locus with alterations of the γ-glutamyl cycle and increased methylglyoxal levels in endothelial cells
37. Association of the 1q25 Diabetes-Specific Coronary Heart Disease Locus With Alterations of the γ-Glutamyl Cycle and Increased Methylglyoxal Levels in Endothelial Cells
38. 1453-P: Adaption of the ACMG/AMP Variant Interpretation Guidelines for GCK, HNF1A, HNF4A-MODY: Recommendations from the ClinGen Monogenic Diabetes Expert Panel
39. Impact of the PPAR-γ2 Pro12Ala Polymorphism and ACE Inhibitor Therapy on New-Onset Microalbuminuria in Type 2 Diabetes: Evidence From BENEDICT
40. Insulin signaling regulating genes: effect on T2DM and cardiovascular risk
41. The TRIB3 Q84R Polymorphism and Risk of Early-Onset Type 2 Diabetes
42. Role of the ENPP1 K121Q Polymorphism in Glucose Homeostasis
43. The ENPP1 K121Q Polymorphism Is Associated With Type 2 Diabetes in European Populations: Evidence From an Updated Meta-Analysis in 42,042 Subjects
44. A Functional Variant of the Adipocyte Glycerol Channel Aquaporin 7 Gene Is Associated With Obesity and Related Metabolic Abnormalities
45. Editorial: The Pleiotropic Effect of the ENPP1 (PC-1) Gene on Insulin Resistance, Obesity, and Type 2 Diabetes
46. The K121Q Polymorphism of the ENPP1/PC-1 Gene Is Associated With Insulin Resistance/Atherogenic Phenotypes, Including Earlier Onset of Type 2 Diabetes and Myocardial Infarction
47. The Functional Q84R Polymorphism of Mammalian Tribbles Homolog TRB3 Is Associated With Insulin Resistance and Related Cardiovascular Risk in Caucasians From Italy
48. The Common −866G/A Polymorphism in the Promoter Region of the UCP-2 Gene Is Associated with Reduced Risk of Type 2 Diabetes in Caucasians from Italy
49. PPARA Polymorphism Influences the Cardiovascular Benefit of Fenofibrate in Type 2 Diabetes: Findings From ACCORD-Lipid
50. The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy
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