نتایج جستجو برای: oxalosis
تعداد نتایج: 170 فیلتر نتایج به سال:
REFERENCES 1 GOLD. Global Strategy for the Diagnosis, Management, and Prevention of COPD, 2011. www.goldcopd.org/Guidelines/guide lines-resources.html Date last accessed: October 1, 2012. 2 Soriano JB, Brusasco V, Dinh-Xuan AT. The European Respiratory Journal makes COPD a priority. Eur Respir J 2011; 38: 999–1001. 3 Bafadhel M, McKenna S, Terry S, et al. Acute exacerbations of COPD: identifica...
We report a case of a woman with secondary oxalosis after jejunoileal bypass surgery for obesity, who presented with oxalate stone disease and renal insufficiency requiring dialysis. Thirty years after surgery, longstanding osteoarticular symptoms were recognized as oxalate arthritis. Eventually, she also developed oxalate vasculitis, which improved with corticoid treatment and intensification ...
Primary hyperoxaluria Type 1 is a rare autosomal recessive inborn error of glyoxylate metabolism, caused by a deficiency of the liver-specific enzyme alanine:glyoxylate aminotransferase. The disorder results in overproduction and excessive urinary excretion of oxalate, causing recurrent urolithiasis and nephrocalcinosis. As glomerular filtration rate declines due to progressive renal involvemen...
We report a case of a woman with secondary oxalosis after jejunoileal bypass surgery for obesity, who presented with oxalate stone disease and renal insufficiency requiring dialysis. Thirty years after surgery, longstanding osteoarticular symptoms were recognized as oxalate arthritis. Eventually, she also developed oxalate vasculitis, which improved with corticoid treatment and intensification ...
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