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Unusual Case of Lipoprotein Glomerulopathy First Diagnosed in a Protocol Kidney Allograft Biopsy.

作者信息

Batal Ibrahim, Fakhoury Gaia, Groopman Emily, D'Agati Vivette D, Morris Heather

机构信息

Department of Pathology and Cell Biology, Columbia University Medical Center, New York, New York, USA.

Department of Medicine, Division of Nephrology, Columbia University Medical Center, New York, New York USA.

出版信息

Kidney Int Rep. 2018 Sep 28;4(2):350-354. doi: 10.1016/j.ekir.2018.09.020. eCollection 2019 Feb.

DOI:10.1016/j.ekir.2018.09.020
PMID:30775634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6365308/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676b/6365308/534e5db1c20f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676b/6365308/793ec346f29b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676b/6365308/534e5db1c20f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676b/6365308/793ec346f29b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676b/6365308/534e5db1c20f/gr2.jpg

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A novel apolipoprotein E mutation, ApoE Ganzhou (Arg43Cys), in a Chinese son and his father with lipoprotein glomerulopathy: two case reports.

本文引用的文献

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Topics in lipoprotein glomerulopathy: an overview.脂蛋白肾小球病专题:概述。
Clin Exp Nephrol. 2014 Apr;18(2):214-7. doi: 10.1007/s10157-013-0887-4. Epub 2013 Oct 23.
2
Hereditary features, treatment, and prognosis of the lipoprotein glomerulopathy in patients with the APOE Kyoto mutation.载脂蛋白 E 京都突变患者脂蛋白肾小球病的遗传特征、治疗和预后。
Kidney Int. 2014 Feb;85(2):416-24. doi: 10.1038/ki.2013.335. Epub 2013 Sep 11.
3
Improvement of nephrotic syndrome by intensive lipid-lowering therapy in a patient with lipoprotein glomerulopathy.
载脂蛋白 E 赣州突变(Arg43Cys)致脂蛋白肾小球病:两例父子病例报告
J Med Case Rep. 2022 Feb 23;16(1):78. doi: 10.1186/s13256-022-03302-0.
4
Case Report: Lipoprotein Glomerulopathy Complicated by Atypical Hemolytic Uremic Syndrome.病例报告:脂蛋白肾小球病合并非典型溶血尿毒症综合征
Front Med (Lausanne). 2021 Jun 2;8:679048. doi: 10.3389/fmed.2021.679048. eCollection 2021.
5
Clinical and genetic analysis of lipoprotein glomerulopathy patients caused by APOE mutations.载脂蛋白 E 基因突变致脂蛋白肾小球病的临床与遗传学分析。
Mol Genet Genomic Med. 2020 Aug;8(8):e1281. doi: 10.1002/mgg3.1281. Epub 2020 May 22.
脂蛋白肾小球病患者强化降脂治疗改善肾病综合征。
Clin Exp Nephrol. 2009 Dec;13(6):659-62. doi: 10.1007/s10157-009-0207-1. Epub 2009 Jul 15.
4
APOE Kyoto mutation in European Americans with lipoprotein glomerulopathy.欧美脂蛋白肾小球病患者中的APOE京都突变
N Engl J Med. 2007 Dec 13;357(24):2522-4. doi: 10.1056/NEJMc072088.
5
A rare cause of posttransplantation nephrotic syndrome.
Am J Kidney Dis. 2005 Jun;45(6):1132-8. doi: 10.1053/j.ajkd.2004.08.048.
6
Interaction of endothelial cells and triglyceride-rich lipoproteins with apolipoprotein E (Arg-->Cys) from a patient with lipoprotein glomerulopathy.
Metabolism. 2002 Feb;51(2):201-5. doi: 10.1053/meta.2002.29990.
7
Apolipoprotein E2/E5 variants in lipoprotein glomerulopathy recurred in transplanted kidney.脂蛋白肾小球病中的载脂蛋白E2/E5变异体在移植肾中复发。
J Am Soc Nephrol. 1999 Jul;10(7):1590-5. doi: 10.1681/ASN.V1071590.
8
Lipoprotein glomerulopathy: a new cause of nephrotic syndrome after renal transplantation.
Nephrol Dial Transplant. 1998 May;13(5):1292-4. doi: 10.1093/ndt/13.5.1292.
9
Lipoprotein glomerulopathy. Report of a normolipidemic case and review of the literature.
Am J Nephrol. 1993;13(1):64-8. doi: 10.1159/000168591.