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Pediatric Nephrology (Berlin, Germany)|November 1, 2008
Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGSRasheed Gbadegesin, Bartlomiej Bartkowiak, Peter J Lavin, et al.Journal of the American Society of Nephrology : JASN|July 10, 2010
A new locus for familial FSGS on chromosome 2pRasheed Gbadegesin, Peter Lavin, Louis Janssens, et al.Journal of the American Society of Nephrology : JASN|January 25, 2011
TRPC6 enhances angiotensin II-induced albuminuriaJason Eckel, Peter J Lavin, Elizabeth A Finch, et al.Journal of the American Society of Nephrology : JASN|August 23, 2014
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGSGentzon Hall, Rasheed A Gbadegesin, Peter Lavin, et al.Pageof 1