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C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and Outcomes.
Wong EKS, Marchbank KJ, Lomax-Browne H, Pappworth IY, Denton H, Cooke K, Ward S, McLoughlin AC, Richardson G, Wilson V, Harris CL, Morgan BP, Hakobyan S, McAlinden P, Gale DP, Maxwell H, Christian M, Malcomson R, Goodship THJ, Marks SD, Pickering MC, Kavanagh D, Cook HT, Johnson SA; MPGN/DDD/C3 Glomerulopathy Rare Disease Group and National Study of MPGN/DDD/C3 Glomerulopathy Investigators. Wong EKS, et al. Among authors: marks sd. Clin J Am Soc Nephrol. 2021 Nov;16(11):1639-1651. doi: 10.2215/CJN.00320121. Epub 2021 Sep 22. Clin J Am Soc Nephrol. 2021. PMID: 34551983 Free PMC article.
Primary hyperoxaluria type 1.
Ajzensztejn MJ, Sebire NJ, Trompeter RS, Marks SD. Ajzensztejn MJ, et al. Among authors: marks sd. Arch Dis Child. 2007 Mar;92(3):197. doi: 10.1136/adc.2006.107334. Arch Dis Child. 2007. PMID: 17337678 Free PMC article. No abstract available.
Multicentre prospective randomised trial of tacrolimus, azathioprine and prednisolone with or without basiliximab: two-year follow-up data.
Webb NJ, Prokurat S, Vondrak K, Watson AR, Hughes DA, Marks SD, Moghal NE, Fitzpatrick MM, Milford DV, Saleem MA, Jones CA, Friman S, Van Damme-Lombaerts R, Janssen F, Hamer C, Rhodes S. Webb NJ, et al. Among authors: marks sd. Pediatr Nephrol. 2009 Jan;24(1):177-82. doi: 10.1007/s00467-008-0931-x. Epub 2008 Aug 8. Pediatr Nephrol. 2009. PMID: 18688657 Clinical Trial.
269 results