KW Perry - Chronic Complex Diseases of Childhood: A …, 2011 - books.google.com ... Definitive diagnosis and differentiation between types I and II hyper- oxaluria is accomplished by measurement of enzyme activity in liver biopsy specimen. ... Prognosis: Untreated primary oxaluria leads to end-stage renal disease anywhere from infancy to adulthood. ... Related articles - All 2 versions
MK Gürgöze… - Pediatric Nephrology, 2011 - Springer ... Hypercalcuria, hyper- oxaluria, hyperuricosuria, and cystinuria was diagnosed if the amounts of those compounds in the urine >4 mg/kg per 24 h, 0.5 mmol (45 mg)/1.73 m2 per 24 h, 815 mg/1.73 m2 per 24 h, and 75 mg/1.73 m2 per 24 h, respectively. ... Cited by 1 - Related articles - All 3 versions
C Cartery, S Faguer, A Karras… - Clinical Journal of the …, 2011 - Am Soc Nephrol ...Oxaluria and Oxalate Metabolism At recognition of AON, daily urinary excretion of ox- alate was 45 mg/d (52 to 92) in the 11 tested patients. None of the patients had a history of ethylene glycol poi- soning or chronic digestive disease. ...oxaluria (n 45 mg/d) 52 90 89 NA 75 ... Related articles - All 2 versions
G Gambaro, MP Ferraro… - Nephrology Dialysis …, 2011 - ERA-EDTA ... We do not have any genuinely effective agents for preventing nephrocalcinosis in primary hyperoxaluria. In 20–30% of primary hyperoxaluric patients, pyridoxine can reduce endogenous oxalate synthesis and oxaluria, but it generally only delays the onset of ESRD. ... Related articles - All 5 versions
M Liebman… - Advances in Nutrition: An International …, 2011 - Am Soc Nutrition ... oxalate bioavailability. Oxalate degradation by oxalate-degrading bacteria within the GIT is another key factor that could affect oxalate absorption and degree of oxaluria. Studies ... bioavailability. Probiotics and oxaluria. As previously ... Cited by 1 - Related articles
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