نتایج جستجو برای: methylmalonic acidemia disorder
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how to cite this article: karimzadeh p, jafari n, ahmad abadi f, jabbehdari s, taghdiri mm, alaee mr, ghofrani m, tonekaboni sh, nejad biglari h. propionic acidemia: diagnosis and neuroimaging findings of this neurometabolic disorder. iran j child neurol. 2014 winter; 8(1):58-61. objective propionic acidemia is one of the rare congenital neurometabolic disorders with autosomal recessive inher...
organic academia are diverse group of disorders characterized by abnormal degredation of specific amino acid in the specific catabolism due to an enzymeactivity defect which mainly due to enzyme deficiency. the majority of the classic organic acid disorders are caused by abnormal catabolism of branched-chain amino acids like lysine. maple syrup urine disease (msud), propionic acidemia, methylma...
Proteinuria as a presenting sign of combined methylmalonic acidemia and homocysteinemia: case report
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