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Complement receptor 1 gene polymorphisms in sarcoidosis.
Zorzetto M, Bombieri C, Ferrarotti I, Medaglia S, Agostini C, Tinelli C, Malerba G, Carrabino N, Beretta A, Casali L, Pozzi E, Pignatti PF, Semenzato G, Cuccia MC, Luisetti M. Zorzetto M, et al. Among authors: pignatti pf. Am J Respir Cell Mol Biol. 2002 Jul;27(1):17-23. doi: 10.1165/ajrcmb.27.1.4805. Am J Respir Cell Mol Biol. 2002. PMID: 12091241
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers.
Gomez-Lira M, Liguori M, Magnani C, Bonamini D, Salviati A, Leone M, Andreoli V, Trojano M, Valentino P, Savettieri G, Quattrone A, Pignatti PF, Momigliano-Richiardi P, Giordano M. Gomez-Lira M, et al. Among authors: pignatti pf. J Neuroimmunol. 2003 Jul;140(1-2):216-21. doi: 10.1016/s0165-5728(03)00208-x. J Neuroimmunol. 2003. PMID: 12864992
Genetic testing for adult-type hypolactasia in Italian families.
Mottes M, Belpinati F, Milani M, Saccomandi D, Petrelli E, Calacoci M, Chierici R, Pignatti PF, Borgna-Pignatti C. Mottes M, et al. Among authors: pignatti pf. Clin Chem Lab Med. 2008;46(7):980-4. doi: 10.1515/CCLM.2008.189. Clin Chem Lab Med. 2008. PMID: 18605960
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study.
Martinelli N, Olivieri O, Shen GQ, Trabetti E, Pizzolo F, Busti F, Friso S, Bassi A, Li L, Hu Y, Pignatti PF, Corrocher R, Wang QK, Girelli D. Martinelli N, et al. Among authors: pignatti pf. BMC Med Genet. 2009 May 13;10:41. doi: 10.1186/1471-2350-10-41. BMC Med Genet. 2009. PMID: 19439088 Free PMC article.
230 results