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.