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Autor:
Louis Janssens, William K. Scott, David N. Howell, Michelle P. Winn, Alison Homstad, Peter J. Conlon, Peter Lavin, Guanghong Wu, Bartlomiej Bartkowiak, Chris Potocky, Elizabeth R. Hauser, Diana Abbott, Jason Eckel, Brandy L. Bowling, Rasheed Gbadegesin
Publikováno v:
Journal of the American Society of Nephrology. 21:1390-1397
FSGS is a clinicopathologic entity characterized by nephrotic syndrome and progression to ESRD. Although the pathogenesis is unknown, the podocyte seems to play a central role in this disorder. Here, we present six kindreds with hereditary FSGS that