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342 related items for PubMed ID: 12631135
1. Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis. Bruschi M, Catarsi P, Candiano G, Rastaldi MP, Musante L, Scolari F, Artero M, Carraro M, Carrea A, Caridi G, Zennaro C, Sanna-Cherchi S, Viola FB, Ferrario F, Perfumo F, Ghiggeri GM. Kidney Int; 2003 Feb; 63(2):686-95. PubMed ID: 12631135 [Abstract] [Full Text] [Related]
2. Depletion of clusterin in renal diseases causing nephrotic syndrome. Ghiggeri GM, Bruschi M, Candiano G, Rastaldi MP, Scolari F, Passerini P, Musante L, Pertica N, Caridi G, Ferrario F, Perfumo F, Ponticelli C. Kidney Int; 2002 Dec; 62(6):2184-94. PubMed ID: 12427144 [Abstract] [Full Text] [Related]
3. Multi-drug resistance-1 gene polymorphisms in nephrotic syndrome: impact on susceptibility and response to steroids. Youssef DM, Attia TA, El-Shal AS, Abduelometty FA. Gene; 2013 Nov 10; 530(2):201-7. PubMed ID: 23994685 [Abstract] [Full Text] [Related]
4. Nephrotic urine prevents increased rat glomerular albumin permeability induced by serum from the same patient with idiopathic nephrotic syndrome. Carraro M, Zennaro C, Candiano G, Musante L, Bruschi M, Ghiggeri GM, Artero M, Faccini L. Nephrol Dial Transplant; 2003 Apr 10; 18(4):689-93. PubMed ID: 12637636 [Abstract] [Full Text] [Related]
5. Apolipoprotein E epsilon 4 allele and nephrotic glomerular diseases in children. Asami T, Ciomartan T, Hayakawa H, Uchiyama M, Tomisawa S. Pediatr Nephrol; 1999 Apr 10; 13(3):233-6. PubMed ID: 10353412 [Abstract] [Full Text] [Related]
6. Association of apoE gene expression and its gene polymorphism with nephrotic syndrome susceptibility: a meta-analysis of experimental and human studies. Zhou TB, Qin YH, Xu HL. Mol Biol Rep; 2012 Oct 10; 39(10):9347-54. PubMed ID: 22760259 [Abstract] [Full Text] [Related]
7. CD80, suPAR and nephrotic syndrome in a case of NPHS2 mutation. Cara-Fuentes G, Araya C, Wei C, Rivard C, Ishimoto T, Reiser J, Johnson RJ, Garin EH. Nefrologia; 2013 Oct 10; 33(5):727-31. PubMed ID: 24089165 [Abstract] [Full Text] [Related]
8. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype. Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L. Clin J Am Soc Nephrol; 2011 Jul 10; 6(7):1626-34. PubMed ID: 21734084 [Abstract] [Full Text] [Related]
9. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis. Besbas N, Kalyoncu M, Cil O, Ozgul RK, Bakkaloglu A, Ozaltin F. Ren Fail; 2015 Jul 10; 37(9):1435-9. PubMed ID: 26335292 [Abstract] [Full Text] [Related]
10. Apolipoprotein E polymorphism and clinical course in childhood nephrotic syndrome. Kim SD, Kim IS, Lee BC, Choi KD, Chung JH, Ihm CG, Cho BS. Pediatr Nephrol; 2003 Mar 10; 18(3):230-3. PubMed ID: 12644914 [Abstract] [Full Text] [Related]
11. Cytotoxic T- Lymphocyte Antigen-4 (CTLA4) Gene Expression and Urinary CTLA4 Levels in Idiopathic Nephrotic Syndrome. Mishra OP, Chhabra P, Narayan G, Srivastava P, Prasad R, Singh A, Abhinay A, Batra VV. Indian J Pediatr; 2019 Jan 10; 86(1):26-31. PubMed ID: 29968132 [Abstract] [Full Text] [Related]
12. Soluble CD40 ligand directly alters glomerular permeability and may act as a circulating permeability factor in FSGS. Doublier S, Zennaro C, Musante L, Spatola T, Candiano G, Bruschi M, Besso L, Cedrino M, Carraro M, Ghiggeri GM, Camussi G, Lupia E. PLoS One; 2017 Jan 10; 12(11):e0188045. PubMed ID: 29155846 [Abstract] [Full Text] [Related]
13. Reduced INF2 expression in nephrotic syndrome is possibly related to clinical severity of steroid resistance in children. Tamura H, Nakazato H, Kuraoka S, Yoneda K, Takahashi W, Endo F. Nephrology (Carlton); 2016 Jun 10; 21(6):467-75. PubMed ID: 26383224 [Abstract] [Full Text] [Related]
14. Toll-like receptor 3 (TLR-3), TLR-4 and CD80 expression in peripheral blood mononuclear cells and urinary CD80 levels in children with idiopathic nephrotic syndrome. Mishra OP, Kumar R, Narayan G, Srivastava P, Abhinay A, Prasad R, Singh A, Batra VV. Pediatr Nephrol; 2017 Aug 10; 32(8):1355-1361. PubMed ID: 28210837 [Abstract] [Full Text] [Related]
15. Serum-soluble urokinase receptor levels do not distinguish focal segmental glomerulosclerosis from other causes of nephrotic syndrome in children. Sinha A, Bajpai J, Saini S, Bhatia D, Gupta A, Puraswani M, Dinda AK, Agarwal SK, Sopory S, Pandey RM, Hari P, Bagga A. Kidney Int; 2014 Mar 10; 85(3):649-58. PubMed ID: 24429405 [Abstract] [Full Text] [Related]
16. Plasma level and genetic variation of apolipoprotein E in patients with lipoprotein glomerulopathy. Zhang B, Liu ZH, Zeng CH, Zheng JM, Chen HP, Zhou H, Li LS. Chin Med J (Engl); 2005 Apr 05; 118(7):555-60. PubMed ID: 15820086 [Abstract] [Full Text] [Related]
17. Urinary protein electrophoresis patterns in childhood idiopathic nephrotic syndrome. Adamson O, Trachtman H, Tejani A. Int J Pediatr Nephrol; 1986 Apr 05; 7(4):181-6. PubMed ID: 2434444 [Abstract] [Full Text] [Related]
18. Synaptopodin expression in idiopathic nephrotic syndrome of childhood. Srivastava T, Garola RE, Whiting JM, Alon US. Kidney Int; 2001 Jan 05; 59(1):118-25. PubMed ID: 11135064 [Abstract] [Full Text] [Related]
19. Trends in the histopathology of childhood nephrotic syndrome in Ibadan Nigeria: preponderance of idiopathic focal segmental glomerulosclerosis. Asinobi AO, Ademola AD, Okolo CA, Yaria JO. BMC Nephrol; 2015 Dec 15; 16():213. PubMed ID: 26670137 [Abstract] [Full Text] [Related]
20. Plasma microRNA-186 and proteinuria in focal segmental glomerulosclerosis. Zhang C, Zhang W, Chen HM, Liu C, Wu J, Shi S, Liu ZH. Am J Kidney Dis; 2015 Feb 15; 65(2):223-32. PubMed ID: 25218681 [Abstract] [Full Text] [Related] Page: [Next] [New Search]