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Autore Titolo Tipo [ Anno(Asc)]
Filtri: Autore è Crovella, Sergio  [Clear All Filters]
2014
da Silva GK, Vianna P, Veit TDegani, Crovella S, Catamo E, Cordero EAlicia Apa, Mattevi VSuñé, Lazzaretti RKuhmmer, Sprinz E, Kuhmmer R, Chies JArtur Bogo. Influence of HLA-G polymorphisms in human immunodeficiency virus infection and hepatitis C virus co-infection in Brazilian and Italian individuals. Infect Genet Evol 2014;21:418-23.
Zupin L, Polesello V, Catamo E, Crovella S, Segat L. Interleukin-10 gene promoter polymorphisms in celiac patients from north-eastern Italy. Hum Immunol 2014;75(7):656-61.
Silva JDe Azevêd, Pancotto JAlexandre, Donadi EAntônio, Crovella S, Sandrin-Garcia P. LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus. Mol Biol Rep 2014;41(4):2249-56.
Bianco AMonica, Girardelli M, Vozzi D, Crovella S, Kleiner G, Marcuzzi A. Mevalonate kinase deficiency and IBD: shared genetic background. Gut 2014;63(8):1367-8.
Kamada AJiro, Pontillo A, Guimarães RLima, Loureiro P, Crovella S, Brandão LAndré Cav. NLRP3 polymorphism is associated with protection against human T-lymphotropic virus 1 infection. Mem Inst Oswaldo Cruz 2014;109(7):960-3.
Catamo E, Zupin L, Crovella S, Celsi F, Segat L. Non-classical MHC-I human leukocyte antigen (HLA-G) in hepatotropic viral infections and in hepatocellular carcinoma. Hum Immunol 2014;75(12):1225-31.
Girardelli M, Vuch J, Tommasini A, Crovella S, Bianco AMonica. Novel missense mutation in the NOD2 gene in a patient with early onset ulcerative colitis: causal or chance association?. Int J Mol Sci 2014;15(3):3834-41.
Travan L, Lega S, Crovella S, Montico M, Panontin E, Demarini S. Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism. J Pediatr 2014;165(1):42-5.

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