Results 91 to 100 of about 3,484 (169)

The hippo-YAP1/TEAD1-SLC7A5 axis: uncovering a novel therapeutic target for oxalate-induced renal tubular ferroptosis

open access: yesRedox Report
Objectives To systematically investigate the regulatory mechanisms of ferroptosis in renal tubular epithelial cells under high oxalate stress, focusing on identifying key upstream signaling pathways and their therapeutic potential.Methods We employed HK ...
Junyi Yang   +9 more
doaj   +1 more source

Acute renal failure after dietary change – a case report

open access: yesBMC Nephrology
Background The disease entity oxalate nephropathy (ON) is an uncommon but devastating cause of chronic kidney disease associated with the deposition of calcium oxalate crystals in the kidney tubules.
Eric Jankowski   +5 more
doaj   +1 more source

Orlistat-induced oxalate nephropathy: an under-recognised cause of chronic kidney disease

open access: yes, 2017
Two patients developed kidney failure due to oxalate deposition in the kidney while taking orlistat. Cessation of orlistat was followed by partial recovery of kidney function.
Laurence Richard Solomon   +7 more
core   +1 more source

Oxalate Nephropathy Following Roux‑en‑Y Gastric Bypass Surgery – Mini‑Review

open access: yes, 2016
Oxalate Nephropathy is characterised by the presence of tubular crystalline deposits of calcium oxalate, which can lead to both acute and chronic tubular injury and progressive renal failure.
Verdelho, M   +5 more
core   +1 more source

A case of oxalate nephropathy presenting with acute kidney injury [PDF]

open access: yesJournal of Krishna Institute of Medical Sciences University
Oxalate Nephropathy (ON) represents a serious condition characterized by a decline in renal function associated with calcium oxalate crystal deposition within renal tubules. It can arise from Primary Hyperoxaluria (PH) due to genetic defects or secondary
Pradnya Mukund Diggikar   +3 more
doaj  

Primary Hyperoxaluria Type 1 with Thrombophilia in Pregnancy: A Case Report

open access: yesCase Reports in Nephrology and Dialysis, 2018
Background: Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease caused by a mutation in the AGXT gene, resulting in deficiency of the alanineglyoxylate:aminotransferase enzyme.
Asma Hasan   +3 more
doaj   +1 more source

Oxalate Nephropathy Secondary to Chronic Pancreatitis: Case Report

open access: yesTurkish Journal of Nephrology, 2019
Chronic pancreatitis is a rare cause of oxalate nephropathy. The aim of this case report was to present a patient hospitalized with acute kidney injury who was diagnosed with oxalate nephropathy and concurrent chronic pancreatitis on further ...
Nergiz BAYRAKCI   +5 more
doaj  

Combined Liver and Kidney Transplant for Primary Hyperoxaluria Type 2

open access: yesIndian Journal of Transplantation
Primary hyperoxaluria type 2 (PH2) is a rare autosomal recessive disorder of oxalate overproduction that frequently leads to end-stage renal disease (ESRD). While isolated kidney transplantation is often performed, it carries a high risk of graft failure
Anjana Raina Misri   +2 more
doaj   +1 more source

Oxalate Nephropathy in an Oxalobacter formigenes–Negative Subject [PDF]

open access: yesKidney International Reports, 2020
Lama Nazzal   +3 more
openaire   +3 more sources

Acute irreversible oxalate nephropathy in a lung transplant recipient treated successfully with a renal transplant

open access: yes, 2012
We report a 29 year old male cystic fibrosis patient with end stage lung disease and normal renal function who underwent a sequential double lung transplant. Medical history included: an ileal resection and pancreatic exocrine dysfunction.
Dheda, Shyam   +5 more
core   +1 more source

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