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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.
Minen F, Cont G, De Cunto A, Martelossi S, Ventura A, Maggiore G, Faletra F, Gasparini P, Cassandrini D. Delayed diagnosis of glycogen storage disease type III. J Pediatr Gastroenterol Nutr 2012;54(1):122-4.
Paloni G, Pastore S, Tommasini A, Lepore L, Taddio A. Delayed reactivation of chronic infantile neurologic, cutaneous, articular syndrome (CINCA) in a patient with somatic mosaicism of CIAS1/NLRP3 gene after withdrawal of anti-IL-1 beta therapy. Clin Exp Rheumatol 2015;33(5):766.
Bose KS, Sarma RH. Delineation of the intimate details of the backbone conformation of pyridine nucleotide coenzymes in aqueous solution. Biochem Biophys Res Commun 1975;66(4):1173-9.
Taddio A, Rossi EDei, Monasta L, Pastore S, Tommasini A, Lepore L, Bronzetti G, Marrani E, Mottolese BD'Agata, Simonini G, Cimaz R, Ventura A. Describing Kawasaki shock syndrome: results from a retrospective study and literature review. Clin Rheumatol 2017;36(1):223-228.

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