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- Urea cycle disorder (UCD) is one of inborn error diseases.Citrullinemia is the most common disease (1/57000) among them, followed by argininosuccinic acidemia (ASA) (1/70000). 摘要尿素循环功能障碍为先天性代谢缺陷的一类，瓜胺酸血症为最常见的一种，发生机率为1/57000；
- The method was used to determine free amino acids in plasma samples fromhospitals and aminoacidopathies such as hyperglycinemia,phenylketonuria,argininosuccinic acidemia,citrullinemia,homocystinuria,maple syrup urine disease and tyrosinemia were detected. 用本法在医院送检的血浆样品中检出了高甘氨酸血症、苯丙酮尿症、精氨琥珀酸血症、胍氨酸血症、同型半胱氨酸尿症、枫糖尿症和酪氨酸血症等氨基酸遗传代谢缺陷症。
- argininosuccinic acidemia 精氨基琥珀酸血症
- How to Manage Lactic Acidemia in HIV-Infected Patients? 如何处理HIV感染病人的乳酸血症?
- The relation between acidemia at birth and deficit in speech/language development should be further evaluated. 产时酸血症和以后的语言发育缺陷间关系需进一步估价。
- Acidemia is believed to be an important cause of bad prognosis and death in pateints with CRF. 酸血症是引起慢性肾衰竭患者预后不良和死亡的重要原因。
- 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;
- The author puts stress on the observation of carbonic acidemia and hemorrhage in anterior skin of neck and chest. 强调观察患者有无严重的高碳酸血症及颈胸前部皮肤出血的重要性。
- 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。
- Hypercholic acidemia is caused bY the interruption of enterohepatic circulation and deterioration of hepatic function after portasystemic shunt. 高胆酸血症主要为门体分流术后肝肠循环阻断和肝功能恶化所致。
- Conclusions Late deceleration may be an indicator of pure metabolic acidemia and complicated variable deceleration be an indicator of mixed acidemia. 结论晚期减速可能是纯代谢性酸血症的一个表现，而异常可变减速可能是混合性酸血症的一个表现。
- 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。
- The pH of the blood is the negative logarithm (- log) of the hydrogen ion (H+) concentration at any given time. Acidemia and alkalified refer to the actual pH of the blood (table 1-1). 血液的pH值是指任一时间H+浓度的负对数（-log）。酸血症和碱血症涉及到血液的实际pH值（表1-1）。
- argininosuccinic acid synthetase 精氨酸琥珀酸合成酶
- Objective To study the transfer of ropivacaine across the single cotyledon of the term human placenta and the effects of maternal hypoproteinemia and fetal acidemia on the transfer. 目的 研究罗哌卡因经离体人胎盘单绒毛叶的转运及母体低蛋白血症和胎儿酸血症对转运的影响。
- argininosuccinic acid synthetase deficiency 精氨琥珀酸合成酶缺乏症
- Among the 223 measurements, alkalemia :acidemia = 3.23:1 . It indicates that alkalemia is the main change of ABD in patients with severe viral hepatitis and the prevention and treatment to alkalemia must be emphasized. 所有223例次中硷血症与酸血症之比为3.;23:1;表明硷血症是重型肝炎ABD的主要改变;必须强调硷血症的防治。
- argininosuccinic aciduria(argininosuccinuria) 精氨(基)琥珀酸尿
- Five cases were diagnosed having propionic acidemia, indic ating GC-MS was more accurate and quick than traditional method for diagnosis a nd differentiate diagnosis of propionic acidemia. 结果检出5例丙酸血症。表明本方法比传统方法能更准确、快速地对丙酸血症作出化学诊断及鉴别诊断。
