398 results on '"Barbetti, Fabrizio"'
Search Results
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. Pathogenesis (of Neonatal Diabetes and Early Onset Diabetes)
5. Permanent neonatal diabetes-causing insulin mutations have dominant negative effects on beta cell identity
6. Monogenic diabetes clinic (MDC): 3-year experience
7. Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients
8. Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation
9. Correction to: Monogenic diabetes clinic (MDC): 3‑year experience
10. The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022
11. School and pre-school children with type 1 diabetes during Covid-19 quarantine: The synergic effect of parental care and technology
12. Permanent Neonatal diabetes-causing Insulin mutations have dominant negative effects on beta cell identity
13. A rare cause of transient neonatal diabetes mellitus (TNDM): spontaneous HNF1B splice variant
14. Not Autoimmune Diabetes Mellitus in Paediatrics
15. Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
16. Genetic causes and treatment of neonatal diabetes and early childhood diabetes
17. 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
18. Insulin therapy in neonatal diabetes mellitus: a review of the literature
19. The expression of four pyridoxal kinase (PDXK) human variants in Drosophila impacts on genome integrity
20. Insulin: still a miracle after all these years
21. ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents
22. Correction to: Monogenic diabetes clinic (MDC): 3‑year experience
23. Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing?
24. Monogenic diabetes clinic (MDC): 3-year experience
25. Editorial: Monogenic diabetes: from genetics and cell biology to clinical practice
26. Very low birth weight newborn with diabetes mellitus due to pancreas agenesis managed with insulin pump reservoir filled with undiluted insulin: 16-month follow-up
27. A possible role of transglutaminase 2 in the nucleus of INS-1E and of cells of human pancreatic islets
28. Neonatal Diabetes: Permanent Neonatal Diabetes and Transient Neonatal Diabetes
29. Not Autoimmune Diabetes Mellitus in Paediatrics
30. Successful treatment of young infants presenting neonatal diabetes mellitus with continuous subcutaneous insulin infusion before genetic diagnosis
31. SGLT2i Improves Glycemic Control in Patients With Congenital Severe Insulin Resistance
32. Review for "Youth-onset type 2 diabetes in Israel: A national cohort"
33. Serological Proteome Analysis (SERPA) as a tool for the identification of new candidate autoantigens in type 1 diabetes
34. The application of precision medicine in monogenic diabetes
35. Sulfonylurea-Insensitive Permanent Neonatal Diabetes Caused by a Severe Gain-of-Function Tyr330His Substitution in Kir6.2
36. Diabetes associated with dominant insulin gene mutations: outcome of 24-month, sensor-augmented insulin pump treatment
37. Review for "Youth-onset type 2 diabetes in Israel: A national cohort"
38. Six cases with severe insulin resistance (SIR) associated with mutations of insulin receptor: Is a Bartter-like syndrome a feature of congenital SIR?
39. Type 2 diabetes in pediatrics
40. Low Prevalence of HNF1A Mutations After Molecular Screening of Multiple MODY Genes in 58 Italian Families Recruited in the Pediatric or Adult Diabetes Clinic From a Single Italian Hospital
41. Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screening
42. Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy
43. No Sign of Proliferative Retinopathy in 15 Patients With Permanent Neonatal Diabetes With a Median Diabetes Duration of 24 Years
44. A rare cause of transient neonatal diabetes mellitus: Spontaneous HNF1B splice variant.
45. Reduced replication fork speed promotes pancreatic endocrine differentiation and controls graft size
46. Review for "An adult patient with permanent neonatal diabetes successfully discontinued insulin therapy after initiating sitagliptin added to sulphonylurea"
47. Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus
48. Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice
49. Review for "An adult patient with permanent neonatal diabetes successfully discontinued insulin therapy after initiating sitagliptin added to sulphonylurea"
50. Long-term follow-up of glycemic and neurological outcomes in an international series of patients with sulfonylurea-treated ABCC8 permanent neonatal diabetes
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.