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Filtri: Autore è Pellegrin, M C  [Clear All Filters]
Journal Article
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.
Taddio A, Pellegrin MC, Gregori M, Wientroub S, Padeh S, Lepore L. Atlanto-axial joint involvement as exclusive manifestation of juvenile idiopathic arthritis (JIA). Clin Exp Rheumatol 2011;29(4):755.

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