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Erroneous genetic risk assessment of Alport syndrome.
Turco AE, Rossetti S, Bresin E, Corrá S. Turco AE, et al. Among authors: bresin e. Lancet. 1995 Nov 4;346(8984):1237. doi: 10.1016/s0140-6736(95)92949-5. Lancet. 1995. PMID: 7475699 No abstract available.
Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an update.
Turco AE, Bresin E, Rossetti S, Englisch S, Pignatti PF, Gammaro L, Maschio G, Bendetti M, Li Vecchi M, Ferrantelli A, Cerasola G, Stiasny B, Schulze B. Turco AE, et al. Among authors: bresin e. Contrib Nephrol. 1997;122:53-7. doi: 10.1159/000059868. Contrib Nephrol. 1997. PMID: 9399039 No abstract available.
Familial haemolytic uraemic syndrome and an MCP mutation.
Noris M, Brioschi S, Caprioli J, Todeschini M, Bresin E, Porrati F, Gamba S, Remuzzi G; International Registry of Recurrent and Familial HUS/TTP. Noris M, et al. Among authors: bresin e. Lancet. 2003 Nov 8;362(9395):1542-7. doi: 10.1016/S0140-6736(03)14742-3. Lancet. 2003. PMID: 14615110
65 results