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Your search keyword '"Barbetti, Fabrizio"' showing total 22 results

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22 results on '"Barbetti, Fabrizio"'

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1. Permanent neonatal diabetes-causing insulin mutations have dominant negative effects on beta cell identity.

2. School and pre-school children with type 1 diabetes during Covid-19 quarantine: The synergic effect of parental care and technology.

3. β Cell Replacement after Gene Editing of a Neonatal Diabetes-Causing Mutation at the Insulin Locus.

4. Genetic causes and treatment of neonatal diabetes and early childhood diabetes.

5. Insulin therapy in neonatal diabetes mellitus: a review of the literature.

6. Successful treatment of young infants presenting neonatal diabetes mellitus with continuous subcutaneous insulin infusion before genetic diagnosis.

7. INS-gene mutations: from genetics and beta cell biology to clinical disease.

8. Sulfonylurea-responsive neonatal diabetes mellitus diagnosed through molecular genetics in two children and in one adult after a long period of insulin treatment.

9. Impaired cleavage of preproinsulin signal peptide linked to autosomal-dominant diabetes.

10. Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).

11. Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies.

12. Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus.

13. Editorial: Personalized therapies for monogenic diabetes.

14. A rare cause of transient neonatal diabetes mellitus: Spontaneous HNF1B splice variant.

15. Insulin: still a miracle after all these years.

16. Role of the ENPP1 K121Q Polymorphism in Glucose Homeostasis.

17. The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapy.

18. Mutational analysis of the coding regions of the genes encoding protein kinase B-alpha and -beta, phosphoinositide-dependent protein kinase-1, phosphatase targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin: lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients.

19. Increased OB gene expression leads to elevated plasma leptin concentrations in patients with chronic primary hyperinsulinemia.

20. Congenital diabetes mellitus

21. Successful treatment of young infants presenting neonatal diabetes mellitus with continuous subcutaneous insulin infusion before genetic diagnosis

22. No sign of proliferative retinopathy in 15 patients with permanent neonatal diabetes with a median diabetes duration of 24 years

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