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208 related items for PubMed ID: 33519811
21. Functional characterization of 105 factor H variants associated with aHUS: lessons for variant classification. Martín Merinero H, Zhang Y, Arjona E, Del Angel G, Goodfellow R, Gomez-Rubio E, Ji RR, Michelena M, Smith RJH, Rodríguez de Córdoba S. Blood; 2021 Dec 02; 138(22):2185-2201. PubMed ID: 34189567 [Abstract] [Full Text] [Related]
22. Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS. Valoti E, Alberti M, Iatropoulos P, Piras R, Mele C, Breno M, Cremaschi A, Bresin E, Donadelli R, Alizzi S, Amoroso A, Benigni A, Remuzzi G, Noris M. Front Immunol; 2019 Dec 02; 10():853. PubMed ID: 31118930 [Abstract] [Full Text] [Related]
23. Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H. de Córdoba SR, de Jorge EG. Clin Exp Immunol; 2008 Jan 02; 151(1):1-13. PubMed ID: 18081690 [Abstract] [Full Text] [Related]
24. An Evaluation of the Complement-Regulating Activities of Human Complement Factor H (FH) Variants Associated With Age-Related Macular Degeneration. Biggs RM, Makou E, Lauder S, Herbert AP, Barlow PN, Katti SK. Invest Ophthalmol Vis Sci; 2022 Nov 01; 63(12):30. PubMed ID: 36445700 [Abstract] [Full Text] [Related]
26. Contribution of functional and quantitative genetic variants of Complement Factor H and Factor H-Related (FHR) proteins on renal pathology. Gómez Delgado I, Sánchez-Corral P. Nefrologia (Engl Ed); 2022 Apr 01; 42(3):280-289. PubMed ID: 36154806 [Abstract] [Full Text] [Related]
27. Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome. Goicoechea de Jorge E, Tortajada A, García SP, Gastoldi S, Merinero HM, García-Fernández J, Arjona E, Cao M, Remuzzi G, Noris M, Rodríguez de Córdoba S. J Am Soc Nephrol; 2018 Jan 01; 29(1):240-249. PubMed ID: 28993505 [Abstract] [Full Text] [Related]
28. Unraveling the Effect of a Potentiating Anti-Factor H Antibody on Atypical Hemolytic Uremic Syndrome-Associated Factor H Variants. Dekkers G, Brouwer MC, Jeremiasse J, Kamp A, Biggs RM, van Mierlo G, Lauder S, Katti S, Kuijpers TW, Rispens T, Jongerius I. J Immunol; 2020 Oct 01; 205(7):1778-1786. PubMed ID: 32848031 [Abstract] [Full Text] [Related]
29. Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome. Abarrategui-Garrido C, Martínez-Barricarte R, López-Trascasa M, de Córdoba SR, Sánchez-Corral P. Blood; 2009 Nov 05; 114(19):4261-71. PubMed ID: 19745068 [Abstract] [Full Text] [Related]
30. CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. Zipfel PF, Wiech T, Stea ED, Skerka C. J Am Soc Nephrol; 2020 Feb 05; 31(2):241-256. PubMed ID: 31980588 [Abstract] [Full Text] [Related]
31. Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN. Wong EK, Anderson HE, Herbert AP, Challis RC, Brown P, Reis GS, Tellez JO, Strain L, Fluck N, Humphrey A, Macleod A, Richards A, Ahlert D, Santibanez-Koref M, Barlow PN, Marchbank KJ, Harris CL, Goodship TH, Kavanagh D. J Am Soc Nephrol; 2014 Nov 05; 25(11):2425-33. PubMed ID: 24722444 [Abstract] [Full Text] [Related]
32. Autoimmune abnormalities of the alternative complement pathway in membranoproliferative glomerulonephritis and C3 glomerulopathy. Noris M, Donadelli R, Remuzzi G. Pediatr Nephrol; 2019 Aug 05; 34(8):1311-1323. PubMed ID: 29948306 [Abstract] [Full Text] [Related]
33. CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome. Piras R, Valoti E, Alberti M, Bresin E, Mele C, Breno M, Liguori L, Donadelli R, Rigoldi M, Benigni A, Remuzzi G, Noris M. Front Immunol; 2022 Aug 05; 13():1011580. PubMed ID: 36793547 [Abstract] [Full Text] [Related]
34. Liver factor B silencing to cure C3 glomerulopathy: Evidence from a mouse model of complement dysregulation. Zanchi C, Locatelli M, Corna D, Cerullo D, Fishilevich E, Desai D, Rottoli D, Donadelli R, Noris M, Zoja C, Remuzzi G, Benigni A. Mol Immunol; 2023 Sep 05; 161():25-32. PubMed ID: 37481826 [Abstract] [Full Text] [Related]
35. Outcome of membranoproliferative glomerulonephritis and C3-glomerulopathy in children and adolescents. Holle J, Berenberg-Goßler L, Wu K, Beringer O, Kropp F, Müller D, Thumfart J. Pediatr Nephrol; 2018 Dec 05; 33(12):2289-2298. PubMed ID: 30238151 [Abstract] [Full Text] [Related]
36. An Engineered Complement Factor H Construct for Treatment of C3 Glomerulopathy. Yang Y, Denton H, Davies OR, Smith-Jackson K, Kerr H, Herbert AP, Barlow PN, Pickering MC, Marchbank KJ. J Am Soc Nephrol; 2018 Jun 05; 29(6):1649-1661. PubMed ID: 29588430 [Abstract] [Full Text] [Related]
37. von Willebrand factor variants in C3 glomerulopathy: A Chinese cohort study. Chen YY, Han SS, Cao Y, Yu XJ, Zhu L, Luo JC, Song WC, Yu F, Mao YH, Zhao MH. Clin Immunol; 2021 Aug 05; 229():108794. PubMed ID: 34245915 [Abstract] [Full Text] [Related]
38. Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration. Triebwasser MP, Roberson ED, Yu Y, Schramm EC, Wagner EK, Raychaudhuri S, Seddon JM, Atkinson JP. Invest Ophthalmol Vis Sci; 2015 Oct 05; 56(11):6873-8. PubMed ID: 26501415 [Abstract] [Full Text] [Related]
39. A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation. Valoti E, Alberti M, Tortajada A, Garcia-Fernandez J, Gastoldi S, Besso L, Bresin E, Remuzzi G, Rodriguez de Cordoba S, Noris M. J Am Soc Nephrol; 2015 Jan 05; 26(1):209-19. PubMed ID: 24904082 [Abstract] [Full Text] [Related]
40. The role of complement in AMD. Zipfel PF, Lauer N, Skerka C. Adv Exp Med Biol; 2010 Jan 05; 703():9-24. PubMed ID: 20711704 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]