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Glomerulosclerosis focal segmental

Ichikawa, I., and Fogo, A. (1996). Focal segmental glomerulosclerosis. Pediatr. Nephrol. 10, 374-391. [Pg.238]

Shirato, I., Hosser, H., Kimura, K., Sakai, T., Tomino, Y., and Kriz, W. (1996). The development of focal segmental glomerulosclerosis in masugi nephritis is based on progressive podocyte damage. Virchows Arch. 429, 255—273. [Pg.244]

Besides congenital nephrotic syndrome of the Finnish type (T6), nephrotic syndrome (with histologic appearance of focal segmental glomerulosclerosis) may result from mutations of other podocyte proteins (T7, K4) (Table 1). [Pg.184]

Nephrotic syndrome may complicate the course of many primary and secondary glomerulopathies. Diabetic nephropathy is the most common cause of nephrotic proteinuria (not always accompanied by full-blown nephrotic syndrome). Lupus nephritis and renal amyloidosis are much rarer secondary glomerulopathies resulting in nephrotic syndrome. The prevalence of primary glomerulopathies differs between Blacks and Whites (focal segmental glomerulosclerosis is more common... [Pg.185]

Dl. Dall Amico, R., Ghiggeri, G., Carraro, M., Artero, M., Ohio, L., Zamorani, E., Zennaro, C., Basile, G., Montini, G., Rivabella, L., Cardillo, M., Scalamogna, M., and Ginevri, F., Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children. Am. J. Kidney Dis. 34, 1048-1055 (1999). [Pg.210]

Ingulli, E., and Tejani, A., Incidence, treatment and outcome of recurrent focal segmental glomerulosclerosis posttransplantation in 42 allografts in children A single-center experience. Transplantation 51, 401—405 (1991). [Pg.212]

Kl. Kambham, N., Tanji, N., Seigle, R. L., Markowitz, G. S., Pulkkinen, L., Uitto, J., and D Agati, V. D., Congenital focal segmental glomerulosclerosis associated with beta4 integrin mutation and epidermolysis bullosa. Am. J. Kidney Dis. 36, 190-196 (2000). [Pg.212]

K4. Kaplan, J., and Poliak, M. R., Familial focal segmental glomerulosclerosis. Curr. Opin. Nephrol. Hypertens. 10, 183-187 (2001). [Pg.212]

K25. Kriz, W., Hahnel, B., Rosener, S., and Eiger, M., Long-term treatment of rats with FGF-2 results in focal segmental glomerulosclerosis. Kidney Int. 48, 1435-1450 (1995). [Pg.213]

L2. Lee, D. Y., Kim, W., and Kang, S. K., Angiotensin-converting enzyme gene polymorphism in patients with minimal-change nephrotic syndrome and focal segmental glomerulosclerosis. Nephron 77,471-473 (1997). [Pg.214]

R3. Rea, R., Smith, C., Sandhu, K., Kwan, J., and Tomson, C., Successful transplant of a kidney with focal segmental glomerulosclerosis. Nephrol. Dial. Transplant. 16,416—417 (2001). [Pg.215]

Sharma, M., Sharma, R., McCarthy, E. T., and Savin, V. J., The FSGS factor Enrichment and in vivo effect of activity from focal segmental glomerulosclerosis plasma. J. Am. Soc. Nephrol. 10, 552-561 (1999). [Pg.216]


See other pages where Glomerulosclerosis focal segmental is mentioned: [Pg.203]    [Pg.231]    [Pg.231]    [Pg.232]    [Pg.238]    [Pg.174]    [Pg.174]    [Pg.179]    [Pg.180]    [Pg.184]    [Pg.184]    [Pg.185]    [Pg.186]    [Pg.186]    [Pg.186]    [Pg.188]    [Pg.188]    [Pg.191]    [Pg.192]    [Pg.192]    [Pg.207]    [Pg.207]    [Pg.209]    [Pg.209]    [Pg.210]    [Pg.210]    [Pg.210]    [Pg.212]    [Pg.216]    [Pg.216]    [Pg.217]    [Pg.217]    [Pg.218]   
See also in sourсe #XX -- [ Pg.73 ]

See also in sourсe #XX -- [ Pg.903 ]




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