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Filtri: Autore è Crovella, S  [Clear All Filters]
Journal Article
Zupin L, Robino A, Navarra CO, Pirastu N, Di Lenarda R, Gasparini P, Crovella S, Bevilacqua L. LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development. Oral Dis 2017;23(7):1001-1008.
Bianco AM, Vuch J, Girardelli M, Zanin V, Marcuzzi A, Crovella S. Letter: inflammatory bowel disease, complementary and alternative medicine, and genetics. Aliment Pharmacol Ther 2012;35(9):1110-1.
Angelo HD, Silva IIFGomes, Oliveira RDR, Louzada-Júnior P, Donadi EA, Crovella S, Maia MMD, de Souza PRE, Sandrin-Garcia P. Interleukin-18, interleukin-12B and interferon-γ gene polymorphisms in Brazilian patients with rheumatoid arthritis: a pilot study. Tissue Antigens 2015;86(4):276-8.
Catamo E, Zupin L, Freato N, Polesello V, Celsi F, Crocè SL, Masutti F, Pozzato G, Segat L, Crovella S. HLA-G regulatory polymorphisms are associated with susceptibility to HCV infection. HLA 2017;89(3):135-142.
Catamo E, Addobbati C, Segat L, T Fragoso S, A Barbosa D, A Dantas T, H Mariz deAtaíde, da Rocha LF, Duarte ALBranco P, Monasta L, Sandrin-Garcia P, Crovella S. HLA-G gene polymorphisms associated with susceptibility to rheumatoid arthritis disease and its severity in Brazilian patients. Tissue Antigens 2014;84(3):308-15.
Segat L, Crovella S. HLA-G 14bp del/ins genetic variation: association with susceptibility to human immunodeficiency virus-1 vertical transmission but not with human immunodeficiency virus-1 infection through horizontal transmission. Tissue Antigens 2012;80(1):12-3.
Segat L, Zupin L, Kim H-Y, Catamo E, Thea DM, Kankasa C, Aldrovandi GM, Kuhn L, Crovella S. HLA-G 14 bp deletion/insertion polymorphism and mother-to-child transmission of HIV. Tissue Antigens 2014;83(3):161-7.
Pellegrin MC, Matarazzo L, Neri E, Pennesi M, Crovella S. HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease. Genet Mol Res 2014;13(2):2669-73.
Crovella S, Moura RR, Cappellani S, Celsi F, Trevisan E, Schneider M, Brollo A, Nicastro EM, Vita F, Finotto L, Zabucchi G, Borelli V. A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma. J Toxicol Environ Health A 2018;81(5):98-105.
Sandrin-Garcia P, Brandão LAC, Guimarães RL, Pancoto JAT, Donadi EA, de Lima-Filho JL, Segat L, Crovella S. Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern Brazilians. Lupus 2012;21(6):625-31.
da Silva MFPTBald, Guimarães V, Silva MAR, Amaral CMMedeiros, Beçak W, Stocco RC, Freitas AC, Crovella S. Frequency of human papillomavirus types 16, 18, 31, and 33 and sites of cervical lesions in gynecological patients from Recife, Brazil. Genet Mol Res 2012;11(1):462-6.
Santos SM, Souza CA, Rabelo KCN, Souza PRE, Moura RR, Oliveira TC, Crovella S. Distribution of forensic marker allelic frequencies in Pernambuco, Northestern Brazil. Genet Mol Res 2015;14(2):4303-10.

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