32 results on '"Massa, Ornella"'
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2. Serological Proteome Analysis (SERPA) as a tool for the identification of new candidate autoantigens in type 1 diabetes
3. Mass Spectrometry-Based Identification Of The Tumor Antigen UN1 as the Transmembrane CD43 Sialoglycoprotein
4. Six cases with severe insulin resistance (SIR) associated with mutations of insulin receptor: Is a Bartter-like syndrome a feature of congenital SIR?
5. Transglutaminase 2 transamidation activity during first-phase insulin secretion: natural substrates in INS-1E
6. No Sign of Proliferative Retinopathy in 15 Patients With Permanent Neonatal Diabetes With a Median Diabetes Duration of 24 Years
7. Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus
8. Estudio de prefactibilidad para la Instalación de una heladería especializada en la elaboración de helados congelados con nitrógeno líquido
9. Neonatal diabetes mellitus due to complete glucokinase deficiency
10. Opposite Clinical Phenotypes of Glucokinase Disease: Description of a Novel Activating Mutation and Contiguous Inactivating Mutations in Human Glucokinase (GCK) Gene
11. Maturity-Onset Diabetes of the Young in Children With Incidental Hyperglycemia: A multicenter Italian study of 172 families
12. Insulin Gene Mutations as Cause of Diabetes in Children Negative for Five Type 1 Diabetes Autoantibodies
13. Permanent Neonatal Diabetes Mellitus (PNDM) in Italy: Molecular Genetics, Time of Onset and Clinical Phenotypes: 1077-P
14. The Second Activating Glucokinase Mutation (A456V): Implications for Glucose Homeostasis and Diabetes Therapy
15. Phosphorylation of seminal vesicle protein IV on Ser58 enhances its peroxidase-stimulating activity
16. Brief Report: Neonatal Diabetes Mellitus Due to Complete Glucokinase Deficiency
17. Mutation screening of the RYR1 gene and identification of two novel mutations in Italian malignant hyperthermia families
18. Renal cysts and diabetes syndrome linked to mutations of the hepatocyte nuclear factor-1β gene: Description of a new family with associated liver involvement
19. Differences in Insulin Secretion and Glucose Tolerance in Children with MODY-2 Carrying or Not Carrying the IRS 1 G972R Variant
20. Short Intravenous Glucose Tolerance Test (IVGTT) Defines a MODY Subtype
21. First-Phase Insulin Response (FPIR) after IVGTT in MODY 2 Patients: Effect of Severity of Mutation
22. Engineered Escherichia coli as new source of flavonoids and terpenoids
23. Transglutaminase 2 transamidation activity during first-phase insulin secretion: natural substrates in INS-1E
24. Opposite Clinical Phenotypes of Glucokinase Disease: Description of a Novel Activating Mutation and Contiguous Inactivating Mutations in Human Glucokinase (GCK) Gene
25. Opposite Clinical Phenotypes of “Glucokinase Disease”: Description of a Novel Activating Mutation and Contiguous Inactivating Mutations in Human Glucokinase Gene
26. KCNJ11activating mutations in Italian patients with permanent neonatal diabetes
27. Role of transglutaminase 2 in glucose tolerance: knockout mice studies and a putative mutation in a MODY patient
28. Protein Kinase C-dependent in VivoPhosphorylation of Prourokinase Leads to the Formation of a Receptor Competitive Antagonist
29. In vitro receptor imaging for characterization of human solid tumors
30. KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.
31. No sign of proliferative retinopathy in 15 patients with permanent neonatal diabetes with a median diabetes duration of 24 years
32. Neonatal Diabetes Mellitus Due to Complete Glucokinase Deficiency.
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