De novo 6.9 Mb interstitial deletion on chromosome 4q31.1-q32.1 in a girl with severe speech delay and dysmorphic features. Am J Med Genet A 2012;158A(4):882-7.
. De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature. Eur J Med Genet 2012;55(2):117-9.
. Dealing with abdominal pain in children affected by systemic lupus erythematosus. Semin Arthritis Rheum 2012;41(4):e3-4.
. DEFB1 gene 5' untranslated region (UTR) polymorphisms in inflammatory bowel diseases. Clinics (Sao Paulo) 2012;67(4):395-8.
. Defective and excessive immunities in pediatric diseases. Curr Pharm Des 2012;18(35):5729-34.
. Delayed diagnosis of glycogen storage disease type III. J Pediatr Gastroenterol Nutr 2012;54(1):122-4.
. Diagnosed child, treated child: food challenge as the first step toward tolerance induction in cow's milk protein allergy. Eur Ann Allergy Clin Immunol 2012;44(2):54-60.
. The dietary paradox in food allergy: yesterday's mistakes, today's evidence and lessons for tomorrow. Curr Pharm Des 2012;18(35):5782-7.
. Does the 1.5 Mb microduplication in chromosome band Xp22.31 have a pathogenetic role? New contribution and a review of the literature. Am J Med Genet A 2012;158A(2):461-4.
. Does the LATCH score assessed in the first 24 hours after delivery predict non-exclusive breastfeeding at hospital discharge?. Breastfeed Med 2012;7(6):423-30.
. Daily practice of mechanical ventilation in Italian pediatric intensive care units: a prospective survey. Pediatr Crit Care Med 2011;12(2):141-6.
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