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目的 提高脉冲激光发射模块的电磁兼容性。方法 基于腔体的电磁屏蔽机理,使用HFSS软件,建立脉冲激光发射模块腔体模型,以电磁敏感度、电磁干扰2个方面对腔体电磁屏蔽效能进行仿真分析。结果 设计的双层屏蔽腔体在电磁波辐照频率为1~100 kHz时,屏蔽效能达到28 dB;电磁波辐照频率为0.2~18 GHz时,屏蔽效能达到47 dB。结论 当电磁波辐照频率在1~100 kHz时,腔体的屏蔽效能随频率的增加而增大。辐射源外部激励时,双层屏蔽腔体使用外层铁内层铜屏蔽效能较高。电磁波辐照频率在0.2~18 GHz时,腔体的屏蔽效能随频率的增大而减小,且发生了谐振效应。当腔体厚度相等时,双层屏蔽的屏蔽效能高于单层屏蔽。使用电缆连接器代替孔洞进行信号传输时,腔体屏蔽效能增加。  相似文献   
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Monochorionic twins are subjected to specific complications which originate in either imbalance or abnormality of the single placenta serving two twins including twin-to-twin transfusion syndrome. The diagnosis is well established in overt clinical forms with the association of polyuric polyhydramnios and oliguric oligohydramnios. The best treatment of cases presenting before 26 weeks of gestion is fetoscopic laser ablation of the intertwin anastomoses on the chorionic plate. Although subjected to subtle variations, the core technique follows robust guidelines which could help understanding and acquiring the required skills and experience to perform this procedure. However appropriate and tailored hands-on training and appropriate perinatal set-up are critical not only for surgical management but also for the follow-up and management of related complications. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   
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Iniencephaly is a rare and lethal congenital malformation of the neural tube characterized by occipital bone defect, cervical dysraphism, fixed retroflexion of the fetal head and severe lordosis of the cervicothoracic spine. The etiology is unknown. Prenatally diagnosed cases of iniencephaly are rare because careful and early ultrasonographic evaluation is necessary. We present three cases of iniencephaly prenatally diagnosed by sonography at 20–22 weeks' gestation in which therapeutic abortion was induced. The sonographic findings were compatible with the postmortem findings. The present cases of iniencephaly were found to carry unusual associated malformations such as two lobes in the right lung and chorangiosis of the placenta. Only hypoplastic lungs have been reported by previous authors. We also studied the 677C→T mutation on the methylenetetrahydrofolate reductase gene in the parents in one of the present cases. The mother was found to be heterozygous for the 677CT polymorphism. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   
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Tuberous sclerosis (TSC) is a frequent autosomal-dominant condition (affecting 1 in 6000 individuals) caused by various mutations in either the hamartin (TSC1) or the tuberin gene (TSC2). This allelic and non-allelic heterogeneity makes genetic counseling and prenatal diagnosis difficult, especially as a significant proportion of TSC cases are due to de novo mutations. For this reason the identification of the disease causing mutation is mandatory for accurate counseling, yet current mutation detection methods such as single-strand conformation polymorphism (SSCP) or denaturing gradient gel electrophoresis (DGGE) are labor intensive with limited detection efficiency. Denaturing high-performance liquid chromatography (DHPLC) is a high-throughput, semi-automated mutation detection system with a reported mutation detection rate close to 100% for PCR fragments of up to 800 bp. We used a recently described DHPLC assay allowing the efficient detection of mutations in TSC1 to analyze the DNA extracted from a chorion villus sample in order to perform a prenatal diagnosis for TSC. The fetus was found not to have inherited the deleterious mutation and the DHPLC diagnosis was confirmed by haplotype analysis. This represents the first DHPLC-based prenatal diagnosis of a genetic disease. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   
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This paper reports an experimental study of the response of the unicellular flagellated algae Dunaliella bioculata to toxic pollutants in water using the 'Doppler laser velocimetry' method. the response to toxic pollutants was encouraging and indicates that Dunaliella bioculata is a good biological model for the detection of toxic pollutants in water.  相似文献   
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