Pubblicazioni Disorders of glucose metabolism in Prader Willi Syndrome: results of a multicentric Italian cohort study Nutr Metab Cardiovasc Dis. 2016 Sep;26(9): 842-7 GAD-treatment of children and adolescents with recent onset type one diabetes preserves residual insulin secretion after 30 months Diabetes Metab Res Rev. 2014 Jul;30(5):405-14. Recomandations for self monitoring in pediatric diabetes: a consensus statement by the ISPAD Acta Diabetol. 2014 Apr;51(2):173-84. Sexual Function in Adult Life Following Passerini-Glaze Feminizing Genitoplasty in Patients with Congenital Adrenal Hyperplasia J Urol. 2014 Jan;191(1):206-11. Necrobiosis lipoidica diabeticorum: a pediatric case report Dermatoendocrinol. 2014 Jan 1;6(1):e27790. Growth hormone therapy and respiratory disorders: long- term follow-up in PWS children J Clin Endocrinol Metab. 2013 Sep;98(9):E1516-23. Rare cases of autoimmune hypothyroidism in young children J Pediatr Endocrinol Metab. 2013;26(9-10):963-6. Congenital Hypothyroidism with Eutopic Thyroid Gland: Analysis of Clinical and Biochemical Features at Diagnosis and After Re-Evaluation J Clin Endocrinol Metab. 2013 Apr;98(4):1395-402. Central Adrenal Insufficiency in Young Adults with Prader-Willi Syndrome Clin Endocrinol (Oxf). 2013 Sep;79(3):371-8. Prader-willi syndrome: clinical aspects J Obes. 2012;2012:473941. Asymptomatic thyrotropin-secreting pituitary macroadenoma in a 13-year-old girl: successful first-line treatment with somatostatin analogs Thyroid. 2012 Oct;22(10):1076-9. Sensor-augmented pump therapy in very young children with type 1 diabetes: an efficacy and feasibility observational study Diabetes Technol Ther. 2012 Sep;14(9):762-4. Asymptomatic Thyrotropin-secreting Pituitary Macroadenoma in a Thirteen Year-old Girl: Successful First-line Treatment with Somatostatin Analogues Diabetes Technol Ther. 2012 Sep;14(9):762-4. Emerging effects of early environmental factors over genetic background for type 1 diabetes susceptibility: evidence from a Nationwide Italian Twin Study J Clin Endocrinol Metab. 2012 Aug;97(8):E1483-91. Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome Clin Endocrinol (Oxf). 2012 Jun;76(6):843-50. 46,XY Karyotype in a Female Phenotype Fetus: A Challenging Diagnosis J Pediatr Adolesc Gynecol. 2012 Jun;25(3):e77-9. Difficult treatment of consumptive hypothyroidism in a child with massive parotid hemangioma J Pediatr Endocrinol Metab. 2012;25(1-2):153-5. Surgical management of pediatric Graves’ disease: an effective definitive treatment Pediatr Surg Int. 2012 Jun;28(6):609-14. GAD65 Antigen Therapy in Recently Diagnosed Type 1 Diabetes Mellitus N Engl J Med. 2012 Feb 2;366(5):433-42. Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome Clin Endocrinol (Oxf). 2012 Jun;76(6):843-50. Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports J Pediatr Endocrinol Metab. 2011;24(9-10):801-5. Early onset of puberty in young girls: an Italian cross-sectional study J Endocrinol Invest. 2012 Oct;35(9):804-8. Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesity Nutr Metab Cardiovasc Dis. 2011 Apr;21(4):269-76. Neurosurgical treatment of craniopharyngioma in adults and children: early and long-term results in a large case series J Neurosurg. 2011 May;114(5):1350-9. Patients’ evaluation of nocturnal hypoglycaemia with GlucoDay continuous glucose monitoring in paediatric patients Acta Diabetol. 2010 Dec;47(4):295-300. Newborn of mothers affected by autoimmune thyroiditis: the importance of thyroid function monitoring in the first months of life Ital J Pediatr. 2010 Mar 10;36:24. Pediatric otorhinolaryngologic manifestations of endocrinological pathologies Int J Pediatr Otorhinolaryngol. 2009 Dec;73 Suppl 1:S49-55. A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs J Pediatr Endocrinol Metab. 2009 Oct;22(10):883-93. The DAWN Youth WebTalk Study: methods, findings, and implications Pediatr Diabetes. 2009 Dec;10 Suppl 13:37-45. Pseudohypoparathyroidism, an often delayed diagnosis: a case series Cases J. 2009 May 28;2:6734. Short-term effects of growth hormone treatment on the upper airways of non severely obese children with Prader-Willi syndrome J Endocrinol Invest. 2009 Jul;32(7):601-5. 17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence J Endocrinol Invest. 2009 Sep;32(8):666-70. A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism Clin Endocrinol (Oxf). 2009 Nov;71(5):739-45. Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene Eur J Endocrinol. 2009 Jun;160(6):1019-23. Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies Diabetes Care. 2009 Jan;32(1):123-5. Decreased parietal cortex activity during mental rotation in children with congenital hypothyroidism Neuroendocrinology. 2009;89(1):56-65. Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity J Allergy Clin Immunol. 2008 Dec;122(6):1105-1112.e1. Recommendations for the diagnosis and management of Prader-Willi syndrome J Clin Endocrinol Metab, November 2008, 93(11):4183–4197 Estrogen exposure in a child from hair lotion used by her mother: clinical and hair analysis data Clin Toxicol (Phila). 2008 Sep;46(8):762-4. Modulating the natural history of type 1 diabetes in children at high genetic risk by mucosal insulin immunization Curr Diab Rep. 2008 Apr;8(2):87-93. The Italian National Survey for Prader-Willi syndrome: an epidemiologic study Am J Med Genet A. 2008 Apr 1;146A(7):861-72. Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism J Clin Endocrinol Metab. 2008 Feb;93(2):605-10. Evidence for in vivo primed and expanded autoreactive T cells as a specific feature of patients with type 1 diabetes J Immunol. 2007 Nov 1;179(9):5785-92. Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy Exp Mol Pathol. 2007 Aug;83(1):59-64.