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Autore [ Titolo(Desc)] Tipo Anno
Filtri: Autore è Crovella, S and First Letter Of Title is H  [Clear All Filters]
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H
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.
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.
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.
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.
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.

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