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A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene.
Frascà GM, Soverini L, Tampieri E, Franceschini G, Calabresi L, Pisciotta L, Preda P, Vangelista A, Stefoni S, Bertolini S. Frascà GM, et al. Among authors: preda p. Nephrol Dial Transplant. 2004 Jun;19(6):1622-4. doi: 10.1093/ndt/gfh179. Nephrol Dial Transplant. 2004. PMID: 15150357 No abstract available.
The role of renal biopsy in the diagnosis of Fabry's disease.
Frascà GM, Canova C, Preda P, Pasquinelli G, Soverini ML, Vangelista A, Stefoni S. Frascà GM, et al. Among authors: preda p. Contrib Nephrol. 2001;(136):211-5. doi: 10.1159/000060190. Contrib Nephrol. 2001. PMID: 11688382 No abstract available.
The role of ultrastructural examination in storage diseases.
Papa V, Tarantino L, Preda P, Badiali De Giorgi L, Fanin M, Pegoraro E, Angelini C, Cenacchi G. Papa V, et al. Among authors: preda p. Ultrastruct Pathol. 2010 Oct;34(5):243-51. doi: 10.3109/01913121003780593. Ultrastruct Pathol. 2010. PMID: 20568989
51 results