Results 21 to 30 of about 2,548 (196)
Saudi Journal of Kidney Diseases and Transplantation, 2014 Renal oxalate deposition can be seen with primary hyperoxaluria, malabsorptive states, ethylene glycol toxicity and, rarely, with excessive vitamin C ingestion.
S Yaich +8 more
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Unusual cause of cerebral calcifications in an 8‐year‐old girl
Clinical Case Reports, 2023 Key Clinical Message Genetic counseling and genetic screening for hyperoxaluria should be recommended for children with urinary lithiasis for early management to avoid progression to oxalosis especially if there is a family history of lithiasis.
Abir Boussetta +3 more
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Oxalate in Foods: Extraction Conditions, Analytical Methods, Occurrence, and Health Implications
Foods, 2023 Oxalate is an antinutrient present in a wide range of foods, with plant products, especially green leafy vegetables, being the main sources of dietary oxalates. This compound has been largely associated with hyperoxaluria, kidney stone formation, and, in
Neuza Salgado +4 more
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Successful strategies for renal transplantation in primary oxalosis [PDF]
, 1984 Successful strategies for renal transplantation in primary oxalosis. Eleven patients, aged 6 months to 47 years, with renal failure due to primary oxalosis, received renal allografts and were followed for 1 to 9 years.
Scheinman, Jon I. +2 more
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Uremia associated with renal oxalosis in a cat [PDF]
, 2019 Renalna oksaloza obilježena je nakupljanjem kristala kalcijeva oksalata u bubrezima što rezultira degeneracijom i nekrozom tubularnih stanica, intersticijskim nefritisom i sklerozom bubrega.
Huber, Doroteja
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Magnetic resonance evaluation of a case with cerebrorenal oxalosis
, 2005 Oxalosis is a rare metabolic disorder in which an enhanced production of oxalic acid leads to hyperoxalemia and deposition of calcium oxalate in different organs.
Durur, I +6 more
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Reversal of oxalosis cardiomyopathy after combined liver and kidney transplantation [PDF]
, 2002 peer reviewedFew data have been published on the course of oxalosis cardiomyopathy after combined liver and kidney transplantation in hyperoxaluria patients with myocardial involvement.
De Roover, Arnaud +21 more
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BMC Nephrology, 2012 Background Oxalosis is a metabolic disorder characterized by deposition of oxalate crystals in various organs including the kidney. Whereas primary forms result from genetic defects in oxalate metabolism, secondary forms of oxalosis can result from ...
Albersmeyer Marc +5 more
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Oxalosis as a complication of chronic renal failure [PDF]
, 1973 Oxalosis as a complication of chronic renal failure. The occurrence of renal and myocardial calcium oxalate deposition was studie at autopsy in patients with normal renal function, acute renal failure, chronic renal failure, and chronic renal failure ...
Salyer, William R., Keren, David
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Thiamine deficiency and oxalosis [PDF]
Journal of Clinical Pathology, 1974 Type I hyperoxaluria results from reduced activity of α-ketoglutarate: glyoxylate carboligase, which is necessary for the synergistic decarboxylation of glyoxylate and α-ketoglutarate to α-hydroxy-β-keto-adipate. Since thiamine pyrophosphate is a cofactor in the reaction, thiamine deficiency might be expected to result in tissue ...
W R, Salyer, D C, Salyer
openaire +2 more sources