Zupin L, Polesello V, Segat L, Kamada AJiro, Kuhn L, Crovella S. DEFB1 polymorphisms and HIV-1 mother-to-child transmission in Zambian population. J Matern Fetal Neonatal Med 2018;:1-7.

Polesello V, Zupin L, Di Lenarda R, Biasotto M, Pozzato G, Ottaviani G, Gobbo M, Crovella S, Segat L. DEFB1 polymorphisms and salivary hBD-1 concentration in Oral Lichen Planus patients and healthy subjects. Arch Oral Biol 2017;73:161-165.

da Silva RCelerino, da Cruz HLacerda Al, Brandão LAndré Cav, Guimarães RLima, Montenegro LMaria Lapa, Schindler HCharifker, Segat L, Crovella S. DEFB1 gene polymorphisms and tuberculosis in a Northeastern Brazilian population. Braz J Microbiol 2016;47(2):389-93.

Zupin L, Polesello V, Grasso DLeonardo, Crovella S, Segat L. DEFB1 polymorphisms and susceptibility to recurrent tonsillitis in Italian children. Int J Pediatr Otorhinolaryngol 2016;83:12-5.

Girardelli M, Arrigo S, Barabino A, Loganes C, Morreale G, Crovella S, Tommasini A, Bianco AMonica. The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency. BMC Pediatr 2015;15(1):208.

da Silva RCelerino, Tavares Nde Alencar, Moura R, Coelho A, Guimarães RLima, Araújo J, Crovella S, Brandão LAndré Cav, Silva Jde Azevêd. DC-SIGN polymorphisms are associated to type 1 diabetes mellitus. Immunobiology 2014;219(11):859-65.

Segat L, Zupin L, Moura RRodrigues, Coelho AVictor Cam, Chagas BSimas, de Freitas ACarlos, Crovella S. DEFB1 polymorphisms are involved in susceptibility to human papillomavirus infection in Brazilian gynaecological patients. Mem Inst Oswaldo Cruz 2014;109(7):918-22.

Zanin V, Segat L, Bianco AMonica, Padovan L, Tavares Nde Alencar, Crovella S. DEFB1 gene 5' untranslated region (UTR) polymorphisms in inflammatory bowel diseases. Clinics (Sao Paulo) 2012;67(4):395-8.