By S. Ogawa, M. Matsumoto, C. Esposito, D. Stern (auth.), Vittorio E. Andreucci M.D., Antonio Dal Canton M.D. (eds.)
' this can be an attractive e-book which should still galvanize notion and dialogue with regards to new healing options in nephrology. 'Nephrology Dialysis Transplant 7 1992
Read or Download New Therapeutic Strategies in Nephrology: Proceedings of the 3rd International Meeting on Current Therapy in Nephrology Sorrento, Italy, May 27–30, 1990 PDF
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Additional info for New Therapeutic Strategies in Nephrology: Proceedings of the 3rd International Meeting on Current Therapy in Nephrology Sorrento, Italy, May 27–30, 1990
And Castello R. Virchows Arch. [Pathol. , Busnach G. Invest. A. Immunol. 2: 283, 1984 36) Camussi G. Kidney Int. , Mannik M. C. Med. M. C. J. Pathol. E. B. lmmunopathol 1980, 15:510-524 42) Schreiner G. M. R. J. Cl in. Invest. R. Kidney Int. R. Kidney Int. C. , and Reuben R. Kidney Int. 1987 vol. C. Kidney Int. 1987 vol. R. , 1982 Churchill Livingstone pp. J. , Seminars in Nephrology, Vol. 9, No 1 (march), 1989: pp. F. Proc. T. T. Exp. Med. R. R. I. lmmunol. , Luft D. C. lnvest. C. , vol. 34 (1988), pp.
DNA-RNA polymerase. d ••n .. rr.. iuion not" ... leontrol sen.. IgG (8) '" '" Zn . O. cn 10 200 0"1 100 800 800 1000 1200 n~S2 IU\:t252 n:45 Pl.... ZnenclterUillIgGl_l•• It ... Zna\lllPl_tther8IIV (n'13) inlr_tnl~or. 130 12. II .. ,. ' ,..... ,.. ' ,...... r-II ...... unfrllC1i_ledl~t. O .... fr ... "ithPtlil ... ICI1l1rectl01 "-'elI) ... 50 50 " " " 1300 1200 ,"'.. '0 .. 2 ,,. bIoforlZn IUppl_t Fi,! ••ft .. Zn~l_t • o Ir __ ft ... I _ t leO In MCNS. In this study we found the positive correlation between plasma zinc level and serum IgG level at an early stage of remission.
4 DISCUSSION Lovastatin in small doses is an effective, safe and well tolerated drug for treating nephrotic hyperlipidemia. Our results are in agreement with two recently reported studies (7,8). The possible mechanisms of lovastatin are based primarily on its ability to inhibit HMG-CoA reductase competitively, thereby reducing the biosynthesis of cholesterol. The reduction in hepatic cellular cholesterol results in a compensatory increase of, receptor-mediated, LDL and IDL catabolism (5). It has been suggested that the drug may also inhibit the hepatic synthesis of lipoproteins contributing to the lipid-lower effect of lovastatin (9).