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- methylmalonic semialdehyde 甲基丙二酸单醛
- methylmalonate semialdehyde 甲基丙二酸半醛
- Objectives To summary the clinical characteristic of l ate onset methylmalonic aciduria (MMA). 目的 总结晚发型甲基丙二酸尿症(MMA)的临床特点。
- At present,the underlying mechanisms of brain injury in methylmalonic acidemia have not yet fully established. 神经节苷脂和突触可塑性异常等脑神经发育损伤;
- Objective Methylmalonic acidemia (MMA) is one of the most common disorders of congenital organic acid metabolism. 目的探讨甲基丙二酸血症(MMA)的临床特征和治疗方法。
- Methylmalonic acidemia is an inherited metabolic disorder, which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin. 甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
- Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin. 甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。
- Objective To explore the value of urease pretreatment-gas chromatography-mass spectrometry(UP-GC-MS) in the diagnosis and therapy of methylmalonic aciduria(MMA). 目的探讨尿素酶预处理-气相色谱-质谱法(UP-GC-MS)在甲基丙二酸尿症(MMA)诊断、治疗中的价值。
- GABA is metabolized by the successive action of GABA transaminase (GABA-T) and succinic semialdehyde dehydrogenase (SSADH), to succinic acid, which is a substrate for the tricarboxylic acid cycle. GABA的降解主要由GABA转氨酶(GABA-T)催化,脱氨基生成琥珀酸半醛,再经琥珀酸半醛脱氢酶(SSADH)催化生成琥珀酸,进入三羧酸循环。
- hydroxymuconate semialdehyde dehydrogenase 羟粘康酸半醛脱氢酶
- aminocarboxymuconic acid semialdehyde decarboxylase 氨羧基粘康酸半醛脱羧酶
- inherited methylmalonic acidemia and homocystinuria 遗传性甲基丙二酸血症和高胱氨酸尿血症
- aspartate semialdehyde dehydrogenase 天门冬氨酸盐半醛脱氢酶
- methyl-phosphinic methylmalonic acid 甲基丁二酸
- succinic semialdehyde dehydrogenase 琥珀酸半醛脱氢酶
- tartronate semialdehyde reductase 羟丙二酸半醛还原酶
- A case of succinic semialdehyde dehydrogenase deficiency 琥珀酸半醛脱氢酶缺陷病一例
- Diagnosis and treatment of methylmalonic acidemia in 14 cases 甲基丙二酸血症14例诊断及治疗分析
- Keywords Methylmalonic acid;Vitamin B12;Mass fragmentography; 甲基丙二酸;维生素B_（12）;碎片质谱法;
- methylmalonic aciduria combined with homocysteinemia 甲基丙二酸尿症
