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Serum Th1 (CXCL10) and Th2 (CCL2) chemokine levels in children with newly diagnosed Type 1 diabetes: a longitudinal study

Diabetic medicine, 2008-11, Vol.25 (11), p.1349-1353

2008

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The genetic abnormality in the beta cell determines the response to an oral glucose load

Diabetologia, 2002-03, Vol.45 (3), p.427-435

2002

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Genetic investigation in an Italian child with an unusual association of atrial septal defect, attributable to a new familial GATA4 gene mutation, and neonatal diabetes due to pancreatic agenesis

Diabetic medicine, 2010-10, Vol.27 (10), p.1195-1200

2010

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Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation

Diabetic medicine, 2008-06, Vol.25 (6), p.651-656

2008

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The ALBA Project: an evaluation of needs, management, fears of Italian young patients with type 1 diabetes in a school setting and an evaluation of parents' and teachers' perceptions

Pediatric diabetes, 2011-08, Vol.12 (5), p.485-493

2011

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AB1171 Use of bone marrow cells (BMCS) added to platelet-rich plasma (PRP) for treatment of bone degenerative processes in jia patient: 18-month follow-up

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.704-704

2013

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Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents

Gene, 2012-12, Vol.511 (2), p.338-340

2012

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Retinopathy screening in patients with Type 1 diabetes diagnosed in young age using a non-mydriatic digital stereoscopic retinal imaging

Journal of endocrinological investigation, 2012-04, Vol.35 (4), p.389-394

2012

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Liver disease as risk factor for cystic fibrosis-related diabetes development

Acta Paediatrica, 2007-05, Vol.96 (5), p.736-739

2007

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T1 diabetes and allergic diseases in children: correspondence to the paper of Thomsen et al., Allergy 2011; 66: 645-647

Allergy (Copenhagen), 2011-12, Vol.66 (12), p.1612-1613

2011

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T1 diabetes and allergic diseases in children

Allergy (Copenhagen), 2011-12, Vol.66 (12), p.1612-1613

2011

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Type 1 diabetes mellitus and asthma: A follow-up study

Allergologia et immunopathologia, 2015-03, Vol.43 (2), p.225-227

2015

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Comment on: Clinical application of best practice guidelines for genetic diagnosis of MODY2

Diabetes research and clinical practice, 2012-02, Vol.95 (2), p.e29-e30

2012

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Re: Body mass index and allergic sensitization in children with asthma or type 1 diabetes

Clinical and experimental allergy, 2011-07, Vol.41 (7), p.1044-1045

2011

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Are psychobiological markers strongly correlated with allostatic load in population with autism spectrum disorders (ASD)?

Medical hypotheses, 2013-04, Vol.80 (4), p.506-506

2013

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Exploring the Molecular Mechanisms of Glucocorticoid Receptor Action from Sensitivity to Resistance

Endocrine development, 2013-01, Vol.24, p.41-56

2013

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Serum transforming growth factor beta 1 during diabetes development in non-obese diabetic mice and humans

Clinical and experimental immunology, 2010-12, Vol.162 (3), p.407-414

2010

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High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI

Diabetologia, 2001-07, Vol.44 (7), p.898-905

2001

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Serum transforming growth factor β1 during diabetes development in non‐obese diabetic mice and humans

Clinical and experimental immunology, 2010-12, Vol.162 (3), p.407-414

2010

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Coeliac disease in 108 patients with juvenile idiopathic arthritis: a 13-year follow-up study

Clinical and experimental rheumatology, 2008-01, Vol.26 (1), p.162

2008

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Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

Journal of inherited metabolic disease, 2001-07, Vol.24 (4), p.448-464

2001

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A telemedicine support for diabetes management: the T-IDDM project

Computer methods and programs in biomedicine, 2002-08, Vol.69 (2), p.147-161

2002

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Estimation of genetic risk for Type 1 diabetes mellitus in newborns on dried blood spot

Journal of endocrinological investigation, 2010-06, Vol.33 (6), p.406-408

2010

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A novel hepatocyte nuclear factor-1β (MODY-5) gene mutation in an Italian family with renal dysfunctions and early-onset diabetes

Diabetologia, 2002-01, Vol.45 (1), p.153-154

2002

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Folic acid, vitamin B12, and homocysteine levels during fasting and after methionine load in patients with Type 1 diabetes mellitus

Journal of endocrinological investigation, 2010-05, Vol.33 (5), p.297-299

2010

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Serum Th1 (CXCL10) and Th2 (CCL2) chemokine levels in children with newly diagnosed Type 1 diabetes: a longitudinal study

The genetic abnormality in the beta cell determines the response to an oral glucose load

Genetic investigation in an Italian child with an unusual association of atrial septal defect, attributable to a new familial GATA4 gene mutation, and neonatal diabetes due to pancreatic agenesis

Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation

The ALBA Project: an evaluation of needs, management, fears of Italian young patients with type 1 diabetes in a school setting and an evaluation of parents' and teachers' perceptions

AB1171 Use of bone marrow cells (BMCS) added to platelet-rich plasma (PRP) for treatment of bone degenerative processes in jia patient: 18-month follow-up

Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents

Retinopathy screening in patients with Type 1 diabetes diagnosed in young age using a non-mydriatic digital stereoscopic retinal imaging

Liver disease as risk factor for cystic fibrosis-related diabetes development

T1 diabetes and allergic diseases in children: correspondence to the paper of Thomsen et al., Allergy 2011; 66: 645-647

T1 diabetes and allergic diseases in children

Type 1 diabetes mellitus and asthma: A follow-up study

Comment on: Clinical application of best practice guidelines for genetic diagnosis of MODY2

Re: Body mass index and allergic sensitization in children with asthma or type 1 diabetes

Are psychobiological markers strongly correlated with allostatic load in population with autism spectrum disorders (ASD)?

Exploring the Molecular Mechanisms of Glucocorticoid Receptor Action from Sensitivity to Resistance

Serum transforming growth factor beta 1 during diabetes development in non-obese diabetic mice and humans

High prevalence of glucokinase mutations in Italian children with MODY. Influence on glucose tolerance, first-phase insulin response, insulin sensitivity and BMI

Serum transforming growth factor β1 during diabetes development in non‐obese diabetic mice and humans

Coeliac disease in 108 patients with juvenile idiopathic arthritis: a 13-year follow-up study

Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

A telemedicine support for diabetes management: the T-IDDM project

Estimation of genetic risk for Type 1 diabetes mellitus in newborns on dried blood spot

A novel hepatocyte nuclear factor-1β (MODY-5) gene mutation in an Italian family with renal dysfunctions and early-onset diabetes

Folic acid, vitamin B12, and homocysteine levels during fasting and after methionine load in patients with Type 1 diabetes mellitus

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