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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 1, 1996
Increased nitric oxide formation in recurrent thrombotic microangiopathies: a possible mediator of microvascular injuryM Noris, P Ruggenenti, M Todeschini, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 5, 2013
Two patients with history of STEC-HUS, posttransplant recurrence and complement gene mutationsM Alberti, E Valoti, R Piras, et al.
British Medical Journal (Clinical Research Ed.)|February 14, 1981
Plasmatic regulation of vascular prostacyclin in pregnancyG Remuzzi, C Zoja, D Marchesi, et al.
Circulation Research|April 1, 1995
Nitric oxide synthesis by cultured endothelial cells is modulated by flow conditionsM Noris, M Morigi, R Donadelli, et al.
Blood|April 1, 1995
Fluid shear stress modulates surface expression of adhesion molecules by endothelial cellsM Morigi, C Zoja, M Figliuzzi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 20, 1998
Pharmacologic control of angiotensin II ameliorates renal disease while reducing renal TGF-beta in experimental mesangioproliferative glomerulonephritisC Zoja, M Abbate, D Corna, et al.
Journal of Lipid Research|December 1, 1989
Development of a mass spectrometric method to quantitate platelet activating factor in mouse urineE Benfenati, D Macconi, M Noris, et al.
Kidney International|July 1, 1993
Methylprednisolone normalizes superoxide anion production by polymorphs from patients with ANCA-positive vasculitidesD Macconi, A F Zanoli, S Orisio, et al.
Lancet (London, England)|August 7, 1999
Renoprotective properties of ACE-inhibition in non-diabetic nephropathies with non-nephrotic proteinuriaP Ruggenenti, A Perna, G Gherardi, et al.
Journal of the American Society of Nephrology : JASN|April 24, 1999
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic PurpuraM Noris, P Ruggenenti, A Perna, et al.
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