oxalic/경색증

The biochemical diagnosis of myocardial infarction is based mainly on the enzyme levels of glutamino-oxalic transaminase (SGOT), lactic dehydrogenase (LDH), and creatine-phosphokinase (CPK). The authors have compared the level of phospho-hexo-isomerase (PHI) with the levels of the three other

Primary hyperoxaluria encompasses 3 rare genetic disorders of glyoxylate metabolism characterized by excessive urinary excretion of oxalic acid, resulting in oxalosis. Patients typically have recurrent calcium oxalate nephrolithiasis and nephrocalcinosis, leading to chronic renal failure and death