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Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations. Ophthalmic Genet 2011;32(4):212-6.
. 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 the adnexal mass. Obstet Gynecol 2011;118(4):956; author reply 956-7.
. Mast cells are critically involved in serum-mediated vascular leakage in chronic urticaria beyond high-affinity IgE receptor stimulation. Allergy 2011;66(12):1538-45.
. The missense variation Q705K in CIAS1/NALP3/NLRP3 gene and an NLRP1 haplotype are associated with celiac disease. Am J Gastroenterol 2011;106(3):539-44.
. Molecular mechanism of glucocorticoid resistance in inflammatory bowel disease. World J Gastroenterol 2011;17(9):1095-108.
. A multicenter, case-control study on risk factors for antepartum stillbirth. J Matern Fetal Neonatal Med 2011;24(3):407-10.
. A multicenter, case-control study on risk factors for antepartum stillbirth. J Matern Fetal Neonatal Med 2011;24(3):407-10.
. A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. Epilepsia 2011;52(4):802-9.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
. Multiple loci are associated with white blood cell phenotypes. PLoS Genet 2011;7(6):e1002113.
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