1Schwartz MM, Lewis EJ. The quarterly case: Nephrotic syndrome in a middle-aged man. Ultrastruct Pathol, 1980, 1 : 575 -582.
2Korbet SM, Schwartz MM, Rosenberg BF, et al. Immunotactoid glomerulopathy. Medicine, 1985, 64 : 228 - 243.
3Fogo A, Qureshi N, Horn RG. Morphologic and clinical features of fibrillary glomerulonephritis versus immunotactoid glomerulopathy. Am J Kidney Dis, 1993, 22:367 -377.
4Bridoux F, Hugue V, Coldefy O, et al. Fibrillary glomerulonephritis and immunotactoid (microtubular) glomerulopathy are associated with distinct immunologic features. Kidney Int, 2002, 62 : 1764 - 1775.
5Rosenstock JL, Markowitz GS, Valeri AM, et al. Fibrillary and immunotactoid glomerulonephritis: distinct entities with different clinical and pathologic features. Kidney Int,2003, 63: 1450-1461.
8Schwartz MM, Korbet SM, Lewis EJ. Immunotactoid Glomerulopathy. J Am Soc Nephrol,2002, 13:1390 -1397.
9Schwartz MM. Glomerular diseases with organized deposits. In: Jennette JC, Olson JL, Schwartz MM, et al. Hepinstall g Pathology of the Kidney ,6th Edition. Lippincott Williams & Wilkins ,2007,912 - 936.
10Ivanyi B, Degrell P. Fibfillary glomerulonephritis and immunotactoid glomerulopathy. Nephrol Dial Transplant ,2004,19 : 2166 - 2170.
二级参考文献21
1章友康,中华内科杂志,1995年,34卷,367页
2Vollmer M, Kremer M, Ruf R, et al . Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evalua2 tion of candidate genes. Genomics, 2000,68 ( 2 ) , 127 - 135.
3Okuda S, Languin LR, Ruoslahti, et al. Elevated expression of transforming growth factor-β and proteoglycan production in experimental glomerulonephritis. Possible role in expansion of the mesangial extracellular matrix. J Clin Invest,1990,86:453 -462.
4Hildebrandt F, Strahm B, Prochoroff A, et al. Glomerulopathy associated with predominant fibronectin deposits : exclusion of the genes for fibronectin, villin and desmin as causative genes. Am J Med Gen- et, 1996, 63(1) :323 -327.
5Zhang Z, Kundu GC, Yuan C J, et al. Severe fibmnectin deposit renal glomerular disease in mice lacking utemglobin. Science, 1997, 276 (5 317) :1408-1412.
6Tuttle SE, Sharma HM, Bay W, Hebert L. A unique familial lobular glomerulopathy. Arch Pathol Lab Med, 1987,111:726 - 731.
8Mazzucco G, Maran E, Rollino C, et al. Glomerulonephritis with organized deposits: a mesangiopathy, not immune complex-mediated disease? Hum Pathol, 1992, 23:63 - 68.
9Assmann K.IM, Koene RAP, Wetzels JFM. Familial glomerulonephritis characterized by massive deposits of fibronectin. Am J Kidney Dis, 1995,25:781 -791.
10Str m EH, Banff G, Krapf R, et al. Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease. Kidney Int, 1995,48:163 - 170 .