Results 1 to 10 of about 6,717 (218)
Hyperoxaluria by the AGXT gene: a case report [PDF]
Journal of Medical Case ReportsBackground This report details a case of AGXT gene mutation in a male patient, 9 years 6 months old, Portuguese ethnicity, with history of nephrocalcinosis and recurrent nephrolithiasis in childhood, which progressed to chronic kidney disease.
Alessandra Vitorino Naghettini +5 more
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The domestic pig as a translational model of hyperoxaluria: a pilot study of acute and chronic sodium oxalate infusion [PDF]
Frontiers in PhysiologyThe purpose of this pilot study was to develop and characterize an in vivo porcine model of hyperoxaluria using intravenous infusion of sodium oxalate (NaOx). Two experimental regimens were developed to replicate acute and follow up chronic hyperoxaluria.
Tomasz Jacek +17 more
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HYPEROXALURIA AND BIOMARKERS OF MUCOSAL IMMUNITY IN PATIENTS WITH RECURRENT PYELONEPHRITIS
Український Журнал Нефрології та Діалізу, 2014 Summary: The aim of our study was to compare the performance of mucosal immunity in urine and saliva of patients with chronic recurrent pyelonephritis subject to availability of hyperoxaluria. Material and methods.
M. Kolesnyk +6 more
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Primary Hyperoxaluria Remains Undiagnosed in Patients with Hyperoxaluria and Recurrent Urolithiasis
Clinical Chemistry, 2007 Primary hyperoxaluria (PH) is a metabolic disorder caused by deficiency of either the liver-specific enzyme alanine:glyoxylate aminotransferase (AGT) for PH type 1 (PH1) or glyoxylate reductase/hydroxypyruvate dehydrogenase (GR/HPR) for PH type 2 (PH2).
van Woerden, Christiaan S. +6 more
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Low Oxalate Diet for Prevention of Kidney Stone Disease: A Literature Review
Scripta Score Scientific Medical JournalBackground: Nephrolithiasis is the most common illness affecting the urinary system. It affects 600,000 Americans annually and about 12% of the world's population.
Mochammad Haikal Alhamdi +1 more
doaj +1 more source
Primary hyperoxaluria in infants
Saudi Journal of Kidney Diseases and Transplantation, 2016 The infantile form of primary hyperoxaluria type-1 (PH-1) is characterized by a rapid progression to the end-stage renal disease (ESRD) due to both increased oxalate load and reduced glomerular filtration rate. In the literature, data on this form are limited.
Manel Jellouli +6 more
openaire +3 more sources
Role of the microflora in distal intestinal tract by maintaining oxalate homeostasis
Annals of Mechnikov's Institute, 2020 Human intestinal microflora is part of the human body and performs numerous function. Considerable research interest is in the field of probiotics for the prevention of kidney stones, which is one of the most common urological diseases.Urolithiasis is ...
T Osolodchenko +5 more
doaj
Microbiota and HostHyperoxaluria is a pathological condition characterized by increased levels of oxalate in the urine, which may result in the deposition of oxalate stones, first in the kidneys, with the risk of incurring chronic kidney disease, and, in the most severe ...
Consuelo Fabi +8 more
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