Results 91 to 100 of about 85,650 (171)

Primary Nonfunction of Renal Allograft Secondary to Acute Oxalate Nephropathy [PDF]

open access: yes, 2011
Primary nonfunction (PNF) accounts for 0.6 to 8% of renal allograft failure, and the focus on causes of PNF has changed from rejection to other causes.
Gampala Reddy   +9 more
core   +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

Transcriptome sequencing and comparative transcriptome analysis of the scleroglucan producer Sclerotium rolfsii [PDF]

open access: yes, 2010
Schmid J, Müller-Hagen D, Bekel T, et al. Transcriptome sequencing and comparative transcriptome analysis of the scleroglucan producer Sclerotium rolfsii. BMC Genomics.
Jochen Schmid   +20 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  

CXCL16 and oxLDL are induced in the onset of diabetic nephropathy [PDF]

open access: yes, 2009
Diabetic nephropathy (DN) is a major cause of end-stage renal failure worldwide. Oxidative stress has been reported to be a major culprit of the disease and increased oxidized low density lipoprotein (oxLDL) immune complexes were found in patients with ...
Amann, Kerstin Ute   +11 more
core   +1 more source

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

Acute Oxalate Nephropathy Associated with Orlistat: A Case Report with a Review of the Literature

open access: yesCase Reports in Nephrology, 2013
Orlistat is a gastrointestinal lipase inhibitor used for weight reduction in obese individuals. Enteric hyperoxaluria caused by orlistat leads to oxalate absorption. Acute oxalate nephropathy is a rare complication of treatment with orlistat.
Dhara Chaudhari   +3 more
doaj   +1 more source

Clinical, genetic and molecular aspects of membranous nephropathy [PDF]

open access: yes, 2011
Membranous Nephropathy (MN) is one of the leading causes of end-stage renal disease (ESRD). MN is an autoimmune disease in which autoantibodies target antigens at the level of the glomerular basement membrane.
Stanescu, H.C.
core  

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  

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

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

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