A Shining Scrotal Fountain. J Pediatr 2015;167(1):205.e1.
. Short Communication FYB polymorphisms in Brazilian patients with type I diabetes mellitus and autoimmune polyglandular syndrome type III. Genet Mol Res 2015;14(1):29-33.
. Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients. Genet Mol Res 2014;13(4):9636-41.
. Should cardiac involvement be included in the criteria for diagnosis of Churg Strauss syndrome?. J Pediatr 2012;160(4):707.
. Shwachman-Diamond syndrome and type 1 diabetes mellitus: more than a chance association?. Exp Clin Endocrinol Diabetes 2011;119(10):610-2.
. The significance of mannose-binding lectin gene polymorphisms on the risk of BK virus coinfection in women with human papillomavirus-positive cervical lesions. Hum Immunol 2011;72(8):663-6.
. Simian virus 40 efficiently infects human T lymphocytes and extends their lifespan. Exp Hematol 2012;40(6):466-76.
. Simultaneous determination of multiple cytokines reveals a pro-inflammatory and pro-angiogenic signature after major cardiothoracic surgery: potential role of C-reactive protein. Cytokine 2012;60(3):593-5.
. Single-day trimethoprim/sulfamethoxazole prophylaxis for Pneumocystis pneumonia in children with cancer. J Pediatr 2014;164(2):389-92.e1.
. A singular case of congenital self-healing histiocytosis with skin, liver and atypical eye involvement. Ocul Immunol Inflamm 2011;19(5):337-9.
. Sirolimus Therapy in Congenital Hyperinsulinism: A Successful Experience Beyond Infancy. Pediatrics 2015;136(5):e1373-6.
. Slow growth: do not forget the thyroid. J Pediatr Gastroenterol Nutr 2012;54(3):438; author reply 438.
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