Results 101 to 110 of about 6,717 (218)
Intestinal barrier dysfunction in hyperoxaluria women with recurrent pyelonephritis
Introduction & Objectives: Nephrolithiasis and prenephrolithiasis states often coexist with recurrent pyelonephritis. The intestine has an important role in the dynamics of oxalate exchange.
Ganna Tolstanova +7 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
Transient hyperoxaluria in a patient with inherited distal renal tubular acidosis
Our observation confirms that hyperoxaluria can be associated with primary dRTA. The explanation of this phenomenon is probably increased intestinal absorption of oxalate in the absence of an intestinal oxalate-degrading bacterium Oxalobacter formigenes.
PELA, IVANA +2 more
core
INTRODUCTION AND AIMS: Antibacterial treatment and long-term antibiotic prophylaxis can disrupt the normal of gut microbiota and lead to violate of oxalate metabolism.
Ganna Tolstanova +4 more
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Recurrence of primary hyperoxaluria: An avoidable catastrophe following kidney transplant
Primary hyperoxaluria is a rare autosomal recessive disease due to deficiency of an oxalate-metabolizing liver enzyme, which results in nephrolithiasis and renal failure.
Murlidharan, P, Madiwale, C, Hase, NK
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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
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
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
The long pentraxin 3 (PTX3) exerts a variety of regulatory functions in acute and chronic tissue inflammation. In particular, PTX3 acts as an opsonin for a variety of pathogens and endogenous particles.
Alberto Mantovani (287283) +10 more
core +1 more source

