Frishberg Y - Search Results

1

Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial.

Frishberg Y, Deschênes G, Groothoff JW, Hulton SA, Magen D, Harambat J, Van't Hoff WG, Lorch U, Milliner DS, Lieske JC, Haslett P, Garg PP, Vaishnaw AK, Talamudupula S, Lu J, Habtemariam BA, Erbe DV, McGregor TL, Cochat P; study collaborators. Frishberg Y, et al. Clin J Am Soc Nephrol. 2021 Jul;16(7):1025-1036. doi: 10.2215/CJN.14730920. Epub 2021 May 13. Clin J Am Soc Nephrol. 2021. PMID: 33985991 Free PMC article. Clinical Trial.

2

[Polymorphisms of the renin-angiotensin system genes in progressive renal disease].

Becker-Cohen R, Frishberg Y. Becker-Cohen R, et al. Among authors: frishberg y. Harefuah. 1998 Feb 1;134(3):200-3. Harefuah. 1998. PMID: 9662913 Review. Hebrew. No abstract available.

3

Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic group.

Rinat C, Wanders RJ, Drukker A, Halle D, Frishberg Y. Rinat C, et al. Among authors: frishberg y. J Am Soc Nephrol. 1999 Nov;10(11):2352-8. doi: 10.1681/ASN.V10112352. J Am Soc Nephrol. 1999. PMID: 10541294

4

Hypothyroidism in primary hyperoxaluria type 1.

Frishberg Y, Feinstein S, Rinat C, Drukker A. Frishberg Y, et al. J Pediatr. 2000 Feb;136(2):255-7. doi: 10.1016/s0022-3476(00)70112-0. J Pediatr. 2000. PMID: 10657836

5

Genetic polymorphism in paraoxonase is a risk factor for childhood focal segmental glomerulosclerosis.

Frishberg Y, Toledano H, Becker-Cohen R, Feigin E, Halle D. Frishberg Y, et al. Am J Kidney Dis. 2000 Dec;36(6):1253-61. doi: 10.1053/ajkd.2000.19842. Am J Kidney Dis. 2000. PMID: 11096050

6

Erythropoietin deficiency causes anemia in nephrotic children with normal kidney function.

Feinstein S, Becker-Cohen R, Algur N, Raveh D, Shalev H, Shvil Y, Frishberg Y. Feinstein S, et al. Among authors: frishberg y. Am J Kidney Dis. 2001 Apr;37(4):736-42. doi: 10.1016/s0272-6386(01)80122-0. Am J Kidney Dis. 2001. PMID: 11273873

7

Familial inheritance of crossed fused renal ectopia.

Rinat C, Farkas A, Frishberg Y. Rinat C, et al. Among authors: frishberg y. Pediatr Nephrol. 2001 Mar;16(3):269-70. doi: 10.1007/s004670000540. Pediatr Nephrol. 2001. PMID: 11322377

8

Severe reversible renal failure due to naproxen-associated acute interstitial nephritis.

Becker-Cohen R, Frishberg Y. Becker-Cohen R, et al. Among authors: frishberg y. Eur J Pediatr. 2001 May;160(5):293-5. doi: 10.1007/s004310100729. Eur J Pediatr. 2001. PMID: 11388597 Review.

9

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. Frishberg Y, et al. J Am Soc Nephrol. 2002 Feb;13(2):400-405. doi: 10.1681/ASN.V132400. J Am Soc Nephrol. 2002. PMID: 11805168

10

Hyperhomocysteinemia in children on renal replacement therapy.

Feinstein S, Sela BA, Drukker A, Becker-Cohen R, Raveh D, Gavendo S, Frishberg Y. Feinstein S, et al. Among authors: frishberg y. Pediatr Nephrol. 2002 Jul;17(7):515-9. doi: 10.1007/s00467-002-0901-7. Epub 2002 Jun 11. Pediatr Nephrol. 2002. PMID: 12172765

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