Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. J Med Genet 2011;48(6):369-74.
. High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. Arthritis Rheum 2011;63(11):3625-32.
. High prevalence of BK polyomavirus sequences in human papillomavirus-16-positive precancerous cervical lesions. J Med Virol 2011;83(10):1770-6.
. High-throughput genotyping robot-assisted method for mutation detection in patients with hypertrophic cardiomyopathy. Diagn Mol Pathol 2011;20(3):175-9.
. HLA-G 14 bp deletion/insertion polymorphism in celiac disease. Am J Gastroenterol 2011;106(1):139-44.
. Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations. Ophthalmic Genet 2011;32(4):212-6.
. In vivo distribution of β2 glycoprotein I under various pathophysiologic conditions. Blood 2011;118(15):4231-8.
. Interventions for the prevention of overweight and obesity in preschool children: a systematic review of randomized controlled trials. Obes Rev 2011;12(5):e107-18.
. Intranasal lidocaine and midazolam for procedural sedation in children. Arch Dis Child 2011;96(2):160-3.
. Letter to the editor: acute effects of intravenous administration of pamidronate in patients with osteoporosis. J Korean Med Sci 2011;26(6):848-9; author reply 850.
. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene. Arthritis Rheum 2011;63(4):1141-50.
. Management of immigration and pregnancy screening in northeastern Italy. Risk Manag Healthc Policy 2011;4:9-13.
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