The work is a literature review, which demonstrates the current view on the mechanisms underlying the formation of hyperoxaluria and possible outcomes. The article includes detailed information on the biochemistry of oxalate, exogenous and endogenous resources in the human body, mechanisms of oxalate absorption in the gastrointestinal tract and renal excretion. Thefinal sectionfocuses on existing andpromising approaches to the treatment ofhyperoxaluria
Mechanisms mediating oxalate-induced alterations in renal have attracted the attention of scientists...
AbstractGlyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a hig...
Primary hyperoxaluria (PH) is a metabolic autosomal recessive disease that causes an error in oxalat...
The work is a literature review, which demonstrates the current view on the mechanisms underlying th...
Hyperoxaluria results from either inherited disorders of glyoxylate metabolism leading to hepatic ox...
Hyperoxaluria leads to urinary calcium oxalate (CaOx) supersaturation, resulting in the formation an...
Primary hyperoxalurias (PHs) are rare inherited disorders of liver glyoxylate metabolism, characteri...
Despite advances in the enzymology, molecular genetics, and clinical knowledge of the primary hypero...
Urolithiasis is a frequent urological condition and oxalate plays an importantrole in kidney stone f...
The article presents modern ideas of hyperoxaluria and oxalate-calcium crystaluria. Oxalic acid meta...
Primary hyperoxalurias are a devastating family of diseases leading to multisystem oxalate depositio...
Oxalosis is an inborn error of metabolism, with autosomal recessive transmission, defined by an exce...
comments in biochemistry Pathogenesis and metabolic defects The primary hyperoxaluric states are cla...
Oxalate is a highly insoluble metabolic waste excreted by the kidneys. Disturbances of oxalate metab...
Enteric Hyperoxaluria (EH) is a metabolic disease caused by excessive absorption of dietary oxalate ...
Mechanisms mediating oxalate-induced alterations in renal have attracted the attention of scientists...
AbstractGlyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a hig...
Primary hyperoxaluria (PH) is a metabolic autosomal recessive disease that causes an error in oxalat...
The work is a literature review, which demonstrates the current view on the mechanisms underlying th...
Hyperoxaluria results from either inherited disorders of glyoxylate metabolism leading to hepatic ox...
Hyperoxaluria leads to urinary calcium oxalate (CaOx) supersaturation, resulting in the formation an...
Primary hyperoxalurias (PHs) are rare inherited disorders of liver glyoxylate metabolism, characteri...
Despite advances in the enzymology, molecular genetics, and clinical knowledge of the primary hypero...
Urolithiasis is a frequent urological condition and oxalate plays an importantrole in kidney stone f...
The article presents modern ideas of hyperoxaluria and oxalate-calcium crystaluria. Oxalic acid meta...
Primary hyperoxalurias are a devastating family of diseases leading to multisystem oxalate depositio...
Oxalosis is an inborn error of metabolism, with autosomal recessive transmission, defined by an exce...
comments in biochemistry Pathogenesis and metabolic defects The primary hyperoxaluric states are cla...
Oxalate is a highly insoluble metabolic waste excreted by the kidneys. Disturbances of oxalate metab...
Enteric Hyperoxaluria (EH) is a metabolic disease caused by excessive absorption of dietary oxalate ...
Mechanisms mediating oxalate-induced alterations in renal have attracted the attention of scientists...
AbstractGlyoxylate detoxification is an important function of human peroxisomes. Glyoxylate is a hig...
Primary hyperoxaluria (PH) is a metabolic autosomal recessive disease that causes an error in oxalat...