Lipoprotein glomerulopathy: a rare cause of steroid-resistant nephrotic syndrome in a child
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13730-024-00861-7.pdf
Reference10 articles.
1. Trautmann A, Boyer O, Hodson E, et al. IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome. Pediatr Nephrol. 2023;38:877–919. https://doi.org/10.1007/s00467-022-05739-3.
2. Matsunaga A, Sasaki J, Komatsu T, Kanatsu K, Tsuji E, Moriyama K, Koga T, Arakawa K, Oikawa S, Saito T, Kita T, Doi T. A novel apolipoprotein E mutation, E2 (Arg25Cys), in lipoprotein glomerulopathy. Kidney Int. 1999;56(2):421–7.
3. Li M-s, Li Y, Liu Y, X-j Z, Zhang H. An updated review and meta analysis of lipoprotein glomerulopathy. Front Med. 2022;9:905007. https://doi.org/10.3389/fmed.2022.905007.
4. Saito T, Matsunaga A, Oikawa S. Impact of lipoprotein glomerulopathy on the relationship between lipids and renal diseases. Am J Kidney Dis. 2006;47(2):199–211. https://doi.org/10.1053/j.ajkd.2005.10.017.
5. Song Y, Yang C, Liu L, Wang H. Case report: a pediatric case of lipoprotein glomerulopathy in china and literature review. Front Pediatr. 2021;9:684814. https://doi.org/10.3389/fped.2021.684814.
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