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125 related items for PubMed ID: 10805468
1. Membranoproliferative glomerulonephritis in two siblings: report and literature review. Bogdanović RM, Dimitrijević JZ, Nikolić VN, Ognjanović MV, Rodić BD, Slavković BV. Pediatr Nephrol; 2000 May; 14(5):400-5. PubMed ID: 10805468 [Abstract] [Full Text] [Related]
3. Familial membranoproliferative glomerulonephritis. Bakkaloglu A, Söylemezoglu O, Tinaztepe K, Saatçi U, Söylemezoglu F. Nephrol Dial Transplant; 1995 May; 10(1):21-4. PubMed ID: 7724023 [Abstract] [Full Text] [Related]
4. Membranoproliferative glomerulonephritis in sibs. Söylemezoğlu O, Tinaztepe K, Bakkaloğlu A, Saatçi U. Turk J Pediatr; 1992 May; 34(4):211-7. PubMed ID: 1306340 [Abstract] [Full Text] [Related]
5. [Sibling cases of nephritis resembling membranoproliferative glomerulonephritis]. Ueda H, Isimura E, Okuno S, Maekawa K, Izumotani T, Kim M, Matsumoto N, Fukumoto S, Imanishi Y, Emoto M, Shoji T, Wanibuchi H, Inaba M, Nishizawa Y. Nihon Jinzo Gakkai Shi; 2002 May; 44(4):420-6. PubMed ID: 12073629 [Abstract] [Full Text] [Related]
6. Familial MPGN - a case series: a clinical description of familial membranoproliferative glomerulonephritis amongst three Irish families. Redahan L, Doyle R, O'Shaughnessy M, Dorman A, Little M, Conlon P. Ren Fail; 2014 Sep; 36(8):1333-6. PubMed ID: 24975727 [Abstract] [Full Text] [Related]
7. Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis. Licht C, Fremeaux-Bacchi V. Thromb Haemost; 2009 Feb; 101(2):271-8. PubMed ID: 19190809 [Abstract] [Full Text] [Related]
8. Pathogenesis of the C3 glomerulopathies and reclassification of MPGN. Bomback AS, Appel GB. Nat Rev Nephrol; 2012 Nov; 8(11):634-42. PubMed ID: 23026947 [Abstract] [Full Text] [Related]
9. Familial membranoproliferative glomerulonephritis type III. Neary J, Dorman A, Campbell E, Keogan M, Conlon P. Am J Kidney Dis; 2002 Jul; 40(1):E1. PubMed ID: 12087587 [Abstract] [Full Text] [Related]
11. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F. J Med Genet; 2007 Mar; 44(3):193-9. PubMed ID: 17018561 [Abstract] [Full Text] [Related]
12. Glomerular paramesangial deposits: association with hypocomplementemia in membranoproliferative glomerulonephritis types I and III. West CD, McAdams AJ. Am J Kidney Dis; 1998 Mar; 31(3):427-34. PubMed ID: 9506679 [Abstract] [Full Text] [Related]
13. Long-term clinical and morphological evaluation of primary membranoproliferative glomerulonephritis. Wu MJ, Shu KH, Chan LP, Lu YS, Cheng CH, Sheu SS, Hsu YH, Lian JD. Zhonghua Yi Xue Za Zhi (Taipei); 1996 Jan; 57(1):34-41. PubMed ID: 8820034 [Abstract] [Full Text] [Related]
14. The Association of Class I and II Human Leukocyte Antigen Serotypes With End-Stage Kidney Disease Due to Membranoproliferative Glomerulonephritis and Dense Deposit Disease. Afolabi H, Zhang BM, O'Shaughnessy M, Chertow GM, Lafayette R, Charu V. Am J Kidney Dis; 2024 Jan; 83(1):79-89. PubMed ID: 37739026 [Abstract] [Full Text] [Related]
15. Clinicopathological features of membranoproliferative glomerulonephritis under a new classification. Nargund P, Kambham N, Mehta K, Lafayette RA. Clin Nephrol; 2015 Dec; 84(6):323-30. PubMed ID: 26445002 [Abstract] [Full Text] [Related]
16. Discordant renal histopathologic findings and complement profiles in membranoproliferative glomerulonephritis type III. Meyers KE, Strife CF, Witzleben C, Kaplan BS. Am J Kidney Dis; 1996 Dec; 28(6):804-10. PubMed ID: 8957031 [Abstract] [Full Text] [Related]
18. Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease). Abrera-Abeleda MA, Nishimura C, Smith JL, Sethi S, McRae JL, Murphy BF, Silvestri G, Skerka C, Józsi M, Zipfel PF, Hageman GS, Smith RJ. J Med Genet; 2006 Jul; 43(7):582-9. PubMed ID: 16299065 [Abstract] [Full Text] [Related]