Results 101 to 110 of about 35,907 (209)

Concurrent Crystalline Light-Chain Proximal Tubulopathy and Membranous Nephropathy: A Case Report and Literature Review

Kidney Medicine
Light-chain proximal tubulopathy (LCPT) is typically characterized by the intracytoplasmic deposition of light chains within the proximal tubular epithelial cells, which is usually classified into crystalline and noncrystalline subgroups.
Huizi Zhang, Chunyun Zhang, Hua Su
doaj   +1 more source

Metabolic Response After a Single Maximal Exercise Session in Physically Inactive Young Adults (EASY Study): Relevancy of Adiponectin Isoforms

Biomolecules
The metabolic response to a maximal exercise test in physically inactive adults remains poorly understood, particularly regarding the role of adiponectin, an adipokine with insulin-sensitizing and anti-inflammatory properties.
Johnattan Cano-Montoya, Amanda Bentes, Yanara Pavez, Paola Rubilar, Carolina Lavoz, Pamela Ehrenfeld, Viviana Sandoval, Sergio Martínez-Huenchullán   +7 more
doaj   +1 more source

Early Detection of Tubulo-Interstitial Kidney Disease in Children Using Highly Discriminating SDS-Gel Electrophoresis

Saudi Journal of Kidney Diseases and Transplantation, 2001
Tubulo-interstitial kidney disease is characterized by moderate proteinuria < 1 g/day of low molecular weight proteins in range of MW 10.000-50.000. Even in the physiological proteinuria of < 150 mg/day, tubulo-interstitial kidney disease may exist.
Al-Bashir A, Rohrmann D, Mertens R, Melzer H, Mann H   +4 more
doaj  

Modelling Lowe syndrome and Dent-2 disease using zebrafish

Frontiers in Cell and Developmental Biology
Lowe syndrome and Dent-2 disease are caused by mutations in the gene encoding OCRL, an inositol 5-phosphatase. The phenotype manifests in the eyes, brain and kidney, with the extra-renal features milder in the case of Dent-2 disease.
Martin Lowe
doaj   +1 more source

Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study

BMC Medical Genomics
Introduction Dent disease type I is a rare X-linked recessive renal tubular disease resulting from pathogenic variants in the CLCN5 gene. Due to the rarity of Dent disease type I and the diversity of its phenotypes, its clinical diagnosis is complex and ...
Ruijue Zhu, Mingming Zhu, Boye Wang, Enen Chen, Danlei Cai, Yinghong Yang, Yi Liang, Chuqi Su, Ding Wang, Xiaofang Sun, Linhuan Huang, Yingjun Xie   +11 more
doaj   +1 more source

4-Phenylbutyric Acid Treatment Reduces Low-Molecular-Weight Proteinuria in a Clcn5 Knock-in Mouse Model for Dent Disease-1. [PDF]

Int J Mol Sci
Perdomo-Ramírez A, Ramos-Trujillo E, Machado JD, García-Nieto V, Mura-Escorche G, Claverie-Martin F, RenalTube Group.   +6 more
europepmc   +1 more source

Idiopathic low molecular weight proteinuria: Report of 4 cases.

Nihon Shoni Jinzobyo Gakkai Zasshi, 1997
Hisashi Yamazaki, Tokushi Nakano, Tetsuo Taguchi   +2 more
openaire   +2 more sources

Treatment of glomerular and tubular proteinuria in the nephrotic range in a female cat: case report. [PDF]

Braz J Vet Med
Pascoal MVDS, Sena G, de Azevedo SF, Intrieri JM, de Souza HJM.   +4 more
europepmc   +1 more source

The Long and the Short of it: How Cubilin Isoforms are Affected by Genetic Variants. [PDF]

Kidney Int Rep
Simons M.
europepmc   +1 more source

The kidney in genetic metabolic disorders. [PDF]

Med Genet
Schultheiss UT, Schumann A.
europepmc   +1 more source