Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene. Arthritis Rheum 2011;63(4):1141-50.
. Levels of anxiety in parents in the 24 hr before and after their child's surgery: A descriptive study. J Clin Nurs 2018;27(1-2):278-287.
. LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus. Mol Biol Rep 2014;41(4):2249-56.
. Letter: TPMT activity and age in IBD patients. Aliment Pharmacol Ther 2012;35(8):966-7; author reply 967-9.
. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Am J Hum Genet 2018;102(3):375-400.
. Lack of Prenylated Proteins, Autophagy Impairment and Apoptosis in SH-SY5Y Neuronal Cell Model of Mevalonate Kinase Deficiency. Cell Physiol Biochem 2017;41(4):1649-1660.
. Long-term follow-up in children with benign convulsions associated with gastroenteritis. Eur J Paediatr Neurol 2014;18(5):572-7.
. Longitudinal study of computerized cardiotocography in early fetal growth restriction. Ultrasound Obstet Gynecol 2017;50(1):71-78.
. Lack of Evidence of Rotavirus-Dependent Molecular Mimicry as a Trigger of Celiac Disease. Clin Exp Immunol 2016;
. Lactotransferrin gene functional polymorphisms do not influence susceptibility to human immunodeficiency virus-1 mother-to-child transmission in different ethnic groups. Mem Inst Oswaldo Cruz 2015;110(2):222-9.
. Lactoferrin gene polymorphisms in Italian patients with recurrent tonsillitis. Int J Pediatr Otorhinolaryngol 2016;88:153-6.
. LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development. Oral Dis 2017;23(7):1001-1008.
.