Rapid Detection of Methylmalonic Acidemia by Derivation and Electrospray Tandem Mass Spectrometry 衍生化电喷雾串联质谱法快速检测甲基丙二酸尿症
Different Types of Acidemia at Birth, Fetal Heart Rate Patterns and Infants Outcome at four Years of Age 产时不同类型胎儿酸血症与胎心监护图形的关系
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。
MRI Diagnosis of Methylmalonic Acidemia in Children 儿童甲基丙二酸血症颅脑常规MRI影像分析
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
Methylmalonic acidemia with initial symptom of coma: clinical analysis of 3 cases 以昏迷为首发症状的甲基丙二酸血症3例临床研究
The patients with COPD often exhibit hypoxia and hyper-carbonic acidemia during rapid eye movement phase. COPD患者睡眠时显著的低氧血症和高碳酸血症发生于快动眼睡眠期。
Decneased C/ P value correlated with neonate umbilical artery blood hypoxia, acidemia and poor perinatal outcome. C/P值的降低与新生儿脐动脉低氧、酸中毒及不良围产儿结局相关。
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。
But the blood PH was significantly lower after aeroperitoneum than before induction ( P 0.01), as acidemia. 血气分析显示,血液pH值在CO2气腹后明显降低(P0.01),呈酸血症。
Electrocardiogram Changes in Rabbit Suffered from Experimental Acidemia 家兔实验性酸血症时的心电图变化
Conclusion Absolute transfer ratio of oxytocin increased with the perfusion time and both maternal hypoproteinemia and fetal acidemia promoted transfer of oxytocin across human placenta. 结论在离体人胎盘单绒毛叶双侧灌注模型中,缩宫素的绝对转运率随时间的延长而增加,母体血低蛋白血症和胎儿血酸血症均增加缩宫素的胎盘转运率。
Objective To improve the pediatrician's knowledge of the relationship between the symptom of coma, ketoacidosis and inborn error of metabolism through the summary of three cases of methylmalonic acidemia ( MMA) with initial symptom of coma. 目的通过对3例以昏迷为主诉而入院的甲基丙二酸血症(MMA)患儿的临床治疗及生化学监测的分析,提高儿科医生对昏迷、酸中毒与遗传代谢性疾病的关系的认识。
3rd. and 4th position on the list. The ratio between alkalemia and acidemia was 2.43 '? 碱血症和酸血症之比为2.43:1。
It was found that respiratory acidosis which appeared selectively in venous blood ( and therefore tissue) was an im-portant component of tissue acidemia during CPR. Arterial blood gases failed to reflect these abnormalities. 结果表明CPR时组织(静脉血)酸血症的重要成分是呼酸,而动脉血气不能反映这一异常。
Late deceleration was associated with pure metabolic acidemia and complicated variable deceleration with mixed acidemia. 减速图形特点显示晚期减速与纯代谢性酸血症有关,而异常可变减速与混合性酸血症有关。
Methylmalonic acidemia is one of the most common disorders of congenital organic acid metabolism. 甲基丙二酸血症是一种常染色体隐性遗传的有机酸血症,在先天性有机酸代谢异常中最为常见。
Definitive diagnosis of methylmalonic acidemia relies on analysis of organic acids in urine by gas-liquid chromatography/ mass spectrometry ( GC/ MS). 目前确诊甲基丙二酸血症有效方法是气相色谱/质谱法(GasChromatography/massSpectrometry,GC/MS)尿有机酸分析。