Works matching AU Barbetti, F.
Results: 21
Mutations in IAPP and NEUROG3 genes are not a common cause of permanent neonatal/infancy/childhood-onset diabetes.
- Published in:
- 2009
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- Publication type:
- Letter
Maturity-onset diabetes of the young in children with incidental hyperglycemia: a multicenter Italian study of 172 families.
- Published in:
- 2009
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- Publication type:
- journal article
Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births.
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- Acta Diabetologica, 2012, v. 49, n. 5, p. 405, doi. 10.1007/s00592-011-0331-8
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- Publication type:
- Article
Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in caucasians.
- Published in:
- 2000
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- Publication type:
- journal article
Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 ( KIR6.2) gene.
- Published in:
- 2006
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- Publication type:
- Letter
Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 ( KIR6.2) mutation.
- Published in:
- 2005
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- Publication type:
- Letter
Permanent diabetes mellitus in the first year of life D. Iafusco et al.: Diabetes mellitus in the first year of life.
- Published in:
- 2003
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- Publication type:
- Erratum
Permanent diabetes mellitus in the first year of life D. Iafusco et al.: Diabetes mellitus in the first year of life.
- Published in:
- Diabetologia, 2002, v. 45, n. 6, p. 798, doi. 10.1007/s00125-002-0837-2
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- Publication type:
- Article
The genetic abnormality in the beta cell determines the response to an oral glucose load.
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- Diabetologia, 2002, v. 45, n. 3, p. 427, doi. 10.1007/s00125-001-0770-9
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- Publication type:
- Article
High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI.
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- Diabetologia, 2001, v. 44, n. 7, p. 898
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- Publication type:
- Article
MODY 2 presenting as neonatal hyperglycaemia: a need to reshape the definition of “neonatal diabetes”?
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- Diabetologia, 2000, v. 43, n. 10, p. 1331
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- Publication type:
- Article
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.
- Published in:
- 2011
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- Publication type:
- journal article
Increased OB gene expression leads to elevated plasma leptin concentrations in patients with chronic primary hyperinsulinemia.
- Published in:
- 1998
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- Publication type:
- journal article
Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresis.
- Published in:
- 1992
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- Publication type:
- journal article
Normal coding sequence of insulin gene in Pima Indians and Nauruans, two groups with highest prevalence of type II diabetes.
- Published in:
- 1991
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- Publication type:
- journal article
Case report: A case of Rabson-Mendenhall syndrome: long-term follow-up and therapeutic management with empagliflozin.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1414451
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- Publication type:
- Article
Synthesis of N-Benzyl Allylamnes by Reductive Amination with Selenophenol Generated Catalytically.
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- Synthetic Communications, 1992, v. 22, n. 6, p. 853, doi. 10.1080/00397919208020849
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- Publication type:
- Article
Single-strand conformation polymorphism analysis of the glucose transporter gene GLUT1 in maturity-onset diabetes of the young.
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- Journal of Molecular Medicine, 2001, v. 79, n. 5/6, p. 270, doi. 10.1007/s001090100220
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- Publication type:
- Article
No beta cell desensitisation after a median of 68 months on glibenclamide therapy in patients with KCNJ11-associated permanent neonatal diabetes.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Permanent diabetes during the first year of life: multiple gene screening in 54 patients.
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- Diabetologia, 2011, v. 54, n. 7, p. 1693, doi. 10.1007/s00125-011-2094-8
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- Publication type:
- Article
TRIB3 R84 variant affects glucose homeostasis by altering the interplay between insulin sensitivity and secretion.
- Published in:
- Diabetologia, 2010, v. 53, n. 7, p. 1354, doi. 10.1007/s00125-010-1749-1
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- Publication type:
- Article