Frishberg Y - Search Results

1

Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1.

Garrelfs SF, Frishberg Y, Hulton SA, Koren MJ, O'Riordan WD, Cochat P, Deschênes G, Shasha-Lavsky H, Saland JM, Van't Hoff WG, Fuster DG, Magen D, Moochhala SH, Schalk G, Simkova E, Groothoff JW, Sas DJ, Meliambro KA, Lu J, Sweetser MT, Garg PP, Vaishnaw AK, Gansner JM, McGregor TL, Lieske JC; ILLUMINATE-A Collaborators. Garrelfs SF, et al. Among authors: frishberg y. N Engl J Med. 2021 Apr 1;384(13):1216-1226. doi: 10.1056/NEJMoa2021712. N Engl J Med. 2021. PMID: 33789010 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

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

6

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.

7

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

8

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

9

Genetic analysis--a diagnostic tool for primary hyperoxaluria type I.

Milosevic D, Rinat C, Batinic D, Frishberg Y. Milosevic D, et al. Among authors: frishberg y. Pediatr Nephrol. 2002 Nov;17(11):896-8. doi: 10.1007/s00467-002-0977-0. Epub 2002 Oct 9. Pediatr Nephrol. 2002. PMID: 12432429

10

Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome.

Frishberg Y, Rinat C, Feinstein S, Becker-Cohen R, Megged O, Schlesinger Y. Frishberg Y, et al. Pediatr Nephrol. 2003 Mar;18(3):273-5. doi: 10.1007/s00467-003-1079-3. Epub 2003 Feb 26. Pediatr Nephrol. 2003. PMID: 12644922

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