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Lipoprotein glomerulopathy: a new cause of nephrotic syndrome after renal transplantation.

作者信息

Mourad G, Djamali A, Turc-Baron C, Cristol J P

机构信息

Department of Nephrology, Lapeyronie University Hospital, Montpellier, France.

出版信息

Nephrol Dial Transplant. 1998 May;13(5):1292-4. doi: 10.1093/ndt/13.5.1292.

DOI:10.1093/ndt/13.5.1292
PMID:9623574
Abstract
摘要

相似文献

1
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.
2
Lipoprotein glomerulopathy: a new cause of nephrotic syndrome after renal transplantation. Implications for renal transplantation.脂蛋白肾小球病:肾移植后肾病综合征的新病因。对肾移植的启示。
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Disappearance of intraglomerular lipoprotein thrombi and marked improvement of nephrotic syndrome by bezafibrate treatment in a patient with lipoprotein glomerulopathy.苯扎贝特治疗脂蛋白肾小球病患者时肾小球内脂蛋白血栓消失及肾病综合征明显改善。
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A newborn infant with lipoprotein glomerulopathy associated with congenital nephrotic syndrome.一名患有与先天性肾病综合征相关的脂蛋白肾小球病的新生儿。
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Lipoprotein glomerulopathy and its pathogenesis.脂蛋白肾小球病及其发病机制。
Contrib Nephrol. 1997;120:30-8. doi: 10.1159/000059821.
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Kidney transplant nephrotic syndrome.肾移植肾病综合征
Am J Med. 1974 Nov;57(5):730-40. doi: 10.1016/0002-9343(74)90846-8.
7
Long-term follow-up of a paediatric case of lipoprotein glomerulopathy.一例儿童脂蛋白肾小球病的长期随访
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Recurrence of lipoprotein glomerulopathy after renal transplantation.肾移植后脂蛋白肾小球病复发
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Rejection-related nephrotic syndrome associated with massive antiglomerular and antitubular basement membrane deposits.与大量抗肾小球和抗肾小管基底膜沉积物相关的排斥反应相关肾病综合征。
Isr J Med Sci. 1985 Nov;21(11):915-8.
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Glomerular beta-lipoprotein in childhood renal diseases.儿童肾脏疾病中的肾小球β脂蛋白
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Normolipidemic lipoprotein glomerulopathy with IgA nephropathy - ApoE Kyoto mutation: a case report.伴有IgA肾病的正常血脂性脂蛋白肾小球病 - 载脂蛋白E京都突变:一例报告
Diagn Pathol. 2025 Apr 5;20(1):36. doi: 10.1186/s13000-025-01636-z.
2
Lipoprotein Glomerulopathy, First Case Report from Canada.脂蛋白肾小球病,加拿大首例病例报告。
Int J Nephrol Renovasc Dis. 2022 Jun 21;15:207-214. doi: 10.2147/IJNRD.S364890. eCollection 2022.
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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.
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.
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Lipoprotein Glomerulopathy in a Hispanic Female: A Case Report and Literature Review.一名西班牙裔女性的脂蛋白肾小球病:病例报告及文献综述
Can J Kidney Health Dis. 2019 Jun 27;6:2054358119859576. doi: 10.1177/2054358119859576. eCollection 2019.
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Unusual Case of Lipoprotein Glomerulopathy First Diagnosed in a Protocol Kidney Allograft Biopsy.首例通过移植肾活检确诊的脂蛋白肾小球病罕见病例
Kidney Int Rep. 2018 Sep 28;4(2):350-354. doi: 10.1016/j.ekir.2018.09.020. eCollection 2019 Feb.
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Long-term outcome of kidney transplantation in a patient with coexisting lipoprotein glomerulopathy and fibrillary glomerulonephritis.一名同时患有脂蛋白肾小球病和纤维样肾小球肾炎患者肾移植的长期预后
Clin Kidney J. 2014 Aug;7(4):396-8. doi: 10.1093/ckj/sfu058. Epub 2014 Jun 17.
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Improvement of nephrotic syndrome by intensive lipid-lowering therapy in a patient with lipoprotein glomerulopathy.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.