Case Report: Acute Renal Infarction in a Child With Coarctation of Aorta
Frontiers in Pediatrics, 2021 Renal arterial infarction can present with hematuria, proteinuria, and hypertension, features often linked to glomerular disease. An aortic aneurysm is an extraordinarily rare complication of coarctation of the aorta.
Qing-Yun Zhang +4 more
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Transgenic zebrafish modeling low-molecular-weight proteinuria and lysosomal storage diseases [PDF]
Kidney International, 2020 Epithelial cells lining the proximal tubule of the kidney reabsorb and metabolize most of the filtered low-molecular-weight proteins through receptor-mediated endocytosis and lysosomal processing. Congenital and acquired dysfunctions of the proximal tubule are consistently reflected by the inappropriate loss of solutes including low-molecular-weight ...
Chen, Zhiyong +6 more
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Large-scale albuminuria screen for nephropathy models in chemically induced mouse mutants [PDF]
, 2005 Background/Aim: Phenotype-driven screening of a great pool of randomly mutant mice and subsequent selection of animals showing symptoms equivalent to human kidney diseases may result in the generation of novel suitable models for the study of the ...
Aigner, B. +6 more
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Dietary interventions to contrast the onset and progression of diabetic nephropathy. a critical survey of new data [PDF]
, 2017 This article is a critical overview of recent contributions on the dietary corrections and the foods that have been claimed to delay or hinder the onset of diabetic nephropathy (DN) and its progression to end-stage renal disease.
Iacobini, Carla +3 more
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Asymptomatic low molecular weight proteinuria.
Nihon Shoni Jinzobyo Gakkai Zasshi, 1997 特発性尿細管性蛋白尿症の母子例を含め3症例を報告した。小児の2例共男児で偶然の機会に尿検査にて異常が発見された。いずれもβ2ミクログロブリンおよび分子量約2.8万の尿中低分子蛋白が増加していた。全例糸球体濾過機能は正常で，発育障害は見られなかった。腎生検を施行した1例において，メサンギウム細胞の増殖はみられず，基質の増加が軽度見られ，またメサンギウム基質の硬化を認めた。
Kaori Tomonaga +3 more
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Noninvasive Urinary Monitoring of Progression in IgA Nephropathy. [PDF]
, 2019 Standard methods for detecting and monitoring of IgA nephropathy (IgAN) have conventionally required kidney biopsies or suffer from poor sensitivity and specificity.
Fervenza, Fernando C +4 more
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Bartter-Like Syndrome as the Initial Presentation of Dent Disease 1: A Case Report
Frontiers in Pediatrics, 2021 Dent disease is a rare genetic disease characterized by low-molecular-weight proteinuria. Dent disease with Bartter-like syndrome is rare and can easily be misdiagnosed and mistreated. Herein, we report a case of Dent disease 1 with Bartter-like syndrome
Qiaoping Chen +4 more
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Urinary retinol binding protein is a marker of the extent of interstitial kidney fibrosis. [PDF]
PLoS ONE, 2014 Currently, a non-invasive method to estimate the degree of interstitial fibrosis (IF) in chronic kidney disease is not available in routine. The aim of our study was to evaluate the diagnostic performance of the measurement of urinary low molecular ...
Nicolas Pallet +11 more
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Low molecular weight proteinuria in Chinese herbs nephropathy
Kidney International, 1995 Urinary excretion of five low molecular weight proteins (LMWP) [beta 2-microglobulin (beta 2m), cystatin C (cyst C), Clara cell protein (CC16), retinol-binding protein (RBP) and alpha 1-microglobulin (alpha 1m)], albumin and N-acetyl-beta-D-glucosaminidase (NAG) were quantified in 16 patients who followed a weight reduction program which included ...
Kabanda, André +4 more
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Experimental rat models of chronic allograft nephropathy: a review [PDF]
, 2014 Chronic allograft nephropathy (CAN) is the leading cause of late allograft loss after renal transplantation (RT), which continues to remain an unresolved problem. A rat model of CAN was first described in 1969 by White et al. Although the rat model of RT
Haylor, John, Shrestha, Badri
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