Yaacov Frishberg
Division of Pediatric Nephrology
Shaare Zedek Medical Center
Jerusalem
Israel
Name/email consistency: high
- Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community. Frishberg, Y., Ben-Neriah, Z., Suvanto, M., Rinat, C., Männikkö, M., Feinstein, S., Becker-Cohen, R., Jalanko, H., Zlotogora, J., Kestilä, M. Genet. Med. (2007)
- The heart of children with steroid-resistant nephrotic syndrome: is it all podocin?. Frishberg, Y., Feinstein, S., Rinat, C., Becker-Cohen, R., Lerer, I., Raas-Rothschild, A., Ferber, B., Nir, A. J. Am. Soc. Nephrol. (2006)
- Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in Israel. Frishberg, Y., Rinat, C., Shalata, A., Khatib, I., Feinstein, S., Becker-Cohen, R., Weismann, I., Wanders, R.J., Rumsby, G., Roels, F., Mandel, H. Am. J. Nephrol. (2005)
- Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome. Frishberg, Y., Rinat, C., Feinstein, S., Becker-Cohen, R., Megged, O., Schlesinger, Y. Pediatr. Nephrol. (2003)
- Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children. Frishberg, Y., Rinat, C., Megged, O., Shapira, E., Feinstein, S., Raas-Rothschild, A. J. Am. Soc. Nephrol. (2002)
