Results 11 to 20 of about 21,048 (245)

Neonatal Proteinuria in Calves—A Quantitative Approach

Animals, 2021
Urine testing is a convenient, non-invasive method of obtaining information about body functions. Depending on the intended purpose, urine testing may be qualitative and/or quantitative. Urine analysis can also include proteins.
Wiesław Skrzypczak, Alicja Dratwa-Chałupnik, Małgorzata Ożgo, Karolina Boniecka   +3 more
doaj   +1 more source

Comparative Study of Fucoidan from Saccharina japonica and Its Depolymerized Fragment on Adriamycin-Induced Nephrotic Syndrome in Rats

Marine Drugs, 2020
Nephrotic syndrome (NS) is a clinical syndrome with a variety of causes, mainly characterized by heavy proteinuria, hypoalbuminemia, and edema. At present, identification of effective and less toxic therapeutic interventions for nephrotic syndrome ...
Jiaojiao Tan, Jing Wang, Lihua Geng, Yang Yue, Ning Wu, Quanbin Zhang   +5 more
doaj   +1 more source

Megalin Knockout Mice as an Animal Model of Low Molecular Weight Proteinuria [PDF]

The American Journal of Pathology, 1999
Megalin is an endocytic receptor expressed on the luminal surface of the renal proximal tubules. The receptor is believed to play an important role in the tubular uptake of macromolecules filtered through the glomerulus. To elucidate the role of megalin in vivo and to identify its endogenous ligands, we analyzed the proximal tubular function in mice ...
Leheste, J.-R., Rolinski, B., Vorum, Henrik, Hilpert, J., Nykjær, Anders; id_orcid 0000-0001-6422-6736, Jacobsen, Christian, Aucouturier, P., Moskaug, J.Ø., Otto, A., Christensen, Erik Ilsø, Willnow, T.E.   +10 more
openaire   +3 more sources

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, Min-Hua Tseng, Min-Hua Tseng, Jhao-Jhuang Ding, Jing-Long Huang   +4 more
doaj   +1 more source

Transgenic zebrafish modeling low-molecular-weight proteinuria and lysosomal storage diseases [PDF]

Kidney International, 2020
Epithelial cells lining the proximal tubule of the kidneyreabsorb and metabolize most of thefiltered low-molecular-weight proteins through receptor-mediatedendocytosis and lysosomal processing. Congenital andacquired dysfunctions of the proximal tubule areconsistently reflected by the inappropriate loss of solutesincluding low-molecular-weight proteins
Chen, Zhiyong, Luciani, Alessandro, Mateos, José María, Barmettler, Gery, Giles, Rachel H, Neuhauss, Stephan C F, Devuyst, Olivier   +6 more
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Low Molecular Weight Proteinuria in Children with Distal Renal Tubular Acidosis [PDF]

PRILOZI, 2018
Abstract Distal renal tubular acidosis (dRTA) (MIM #267300, #602722 and #179800) is a rare inherited tubulopathy characterized by the inability of the distal tubule to acidify the urine with consecutive systemic acidosis. The clinical features include polyuria, polydipsia, poor appetite, failure to thrive, short stature and rickets ...
Shpetim, Salihu, Katerina, Tosheska, Svetlana, Cekovska, Zoran, Gucev, Momir, Polenakovic, Velibor, Tasic   +5 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, Kikuo Iitaka, Takeo Ishidate, Takashi Nishikawa   +3 more
openaire   +2 more sources

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, Jadoul, Michel, Lauwerys, Robert, Bernard, Alfred, van Ypersele de Strihou, Charles   +4 more
openaire   +2 more sources

Making a Dent in Dent Disease

Function, 2020
Dent disease (DD) is a rare kidney disorder caused by mutations in the Cl−/H+ exchanger ClC-5. Extensive physiologic characterization of the transporter has begun to illuminate its role in endosomal ion homeostasis.
Katherine E Shipman, Ora A Weisz
doaj   +1 more source

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, Yan Cao, Liyun Xu, Jingqi Liu, Xiaochuan Wu   +4 more
doaj   +1 more source