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Floridia M, Tamburrini E, Anzidei G, Tibaldi C, Muggiasca ML, Guaraldi G, Fiscon M, Vimercati A, Martinelli P, Donisi A, Dalzero S, Ravizza M. Declining HCV seroprevalence in pregnant women with HIV. Epidemiol Infect 2010;138(9):1317-21.
Marcuzzi A, Decorti G, Pontillo A, Ventura A, Tommasini A. Decreased cholesterol levels reflect a consumption of anti-inflammatory isoprenoids associated with an impaired control of inflammation in a mouse model of mevalonate kinase deficiency. Inflamm Res 2010;59(5):335-8.
Secchiero P, Perri P, Melloni E, Martini A, Lamberti G, Sebastiani A, Zauli G. Decreased levels of soluble TNF-related apoptosis-inducing ligand (TRAIL) in the conjunctival sac fluid of patients with diabetes affected by proliferative retinopathy. Diabet Med 2011;28(10):1277-8.
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.
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, 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.
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.
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.
Notarangelo LDaniele, Tommasini A. Defective and excessive immunities in pediatric diseases. Curr Pharm Des 2012;18(35):5729-34.
Olivito B, Taddio A, Simonini G, Massai C, Ciullini S, Gambineri E, de Martino M, Azzari C, Cimaz R. Defective FOXP3 expression in patients with acute Kawasaki disease and restoration by intravenous immunoglobulin therapy. Clin Exp Rheumatol 2010;28(1 Suppl 57):93-7.
Cappelli E, Cuccarolo P, Stroppiana G, Miano M, Bottega R, Cossu V, Degan P, Ravera S. Defects in mitochondrial energetic function compels Fanconi Anaemia cells to glycolytic metabolism. Biochim Biophys Acta Mol Basis Dis 2017;1863(6):1214-1221.

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