Results 101 to 110 of about 9,955 (227)
Primary hyperoxaluria Type 1: organic aciduria diagnosed in plasma [PDF]
Background: Primary hyperoxaluria Type 1 (PH1) is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the liver-specific peroxisomal enzyme alanine:glyoxylate aminotransferase.
Dias, Aureliano +3 more
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Multiomics Assessment of the Gut Microbiome in Rare Hyperoxaluric Conditions
Introduction: Hyperoxaluria is a risk factor for kidney stone formation and chronic kidney disease progression. The microbiome is an important protective factor against oxalate accumulation through the activity of its oxalate-degrading enzymes (ODEs). In
Nadim Zaidan +12 more
doaj +1 more source
Complex system modeling reveals oxalate homeostasis is driven by diverse oxalate-degrading bacteria
Decades of research have made clear that host-associated microbiomes touch all facets of health. However, effective therapies that target the microbiome have been elusive given its inherent complexity.
Sromona D Mukherjee +10 more
doaj +1 more source
Protective effects of the aqueous extract of Crocus sativus against ethylene glycol induced nephrolithiasis in rats [PDF]
This study evaluated the possible protective effect of Crocus sativus L. (saffron) in the treatment of renal calculi. Aqueous extract of saffron (25, 50 and 100 mg/kg, daily) was administered intraperitoneally in two regimens of protective or curative ...
Amin, Bahareh +4 more
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The mechanisms and conditions under which urinary stones, pathological biominerals in the kidneys and bladder, are formed have not yet been fully clarified.
Anamarija Stanković +6 more
doaj +1 more source
Tamm-Horsfall protein in recurrent calcium kidney stone formers with positive family history: abnormalities in urinary excretion, molecular structure and function [PDF]
Tamm-Horsfall protein (THP) powerfully inhibits calcium oxalate crystal aggregation, but structurally abnormal THPs from recurrent calcium stone formers may promote crystal aggregation.
Hess, Bernhard +3 more
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Primary hyperoxaluria (PH) type 1 is a rare autosomal recessive disorder of glyoxylate metabolism. Its prevalence is 1–3 cases/million people. Glyoxylate is the precursor of oxalate which is believed to be produced by oxidation in liver peroxisomes ...
Charusheela Rajesh Gore +2 more
doaj +1 more source

