可编程控制器在化肥散运系统上的应用

整个散运系统采用３台ＦＸ２－１２８ＭＲＰＬＣ分块控制后，使得控制结构清楚，线路简单，工作可靠性大为提高，对所有控制柜元器件进行数据库管理，极大地提高图表的准确率。     

高镁瓷工艺特性研究和应用

本文总结了ＭｇＯ－ＳｉＯ２－Ａｌ２Ｏ３系的高镁瓷配方、增塑及烧成工艺特性的研究过程与应用结果；介绍了适应大生产的高镁瓷制作工艺。     

复印粉的粉碎分级技术

本文介绍了利用国产气流粉碎机和余气萃取分级制备复印粉的实用技术，并展示了粉碎分级系统和复印粉的电镜照片。     

矿化剂对氧化铬绿色釉呈色性能的影响

针对氧化铬绿色釉存在色调暗不够鲜艳的缺点，研究了矿化剂对其呈色性能的影响，经分光光度分析的扫描电镜测试，表明矿化剂具有一定的助熔作用和还原性，从而提高了氧化铬绿色釉的鲜艳度和着色力，增强了装饰性，同时矿化剂还能降低烧成温度，节约能源，具有应用价值。     

受控离散事件过程（CDEP）的一种代数分析方法

本文在文［１～３］的基础上，提出了受控离散事件过程（ＣＤＥＰ）的一种代数分析方法，弥补了Ｒａｍａｄｇｅ和Ｗｏｎｈａｍ［１～３］的理论对具体系统的应用缺乏可操作性的缺陷，使得对ＣＤＥＰ动态过程的分析变得更为直观，同时也使控制器的设计过程更具可操作性．     

晶体管的计算机辅助设计

将晶体管设计中繁琐的纵向、横向参数的设计计算以及参数验算,采用Basic人机对话方式,由计算机完成。并用BAsic语言绘制出所需的七块光刻掩膜图。既大大地减轻了设计人员繁琐劳动、缩短了设计时间、提高设计质量,又便于修改。还可广泛用于同种结构的不同动率要求的各种晶体管的设计中。     

Prognostic factors of early sequelae and fatal outcome of Japanese encephalitis

A clinical case control study to identify prognostic factors present at hospital admission associated with early sequelae and fatal outcome of acute Japanese encephalitis (JE) was carried out in Gusi county, Henan Province, central China from June to September 1991. A total of 70 patients with laboratory-confirmed acute JE were studied, of whom 3 cases died and 33 cases had neurological or psychiatric sequelae at the end of three months follow-up. The results showed that acute JE at younger age, with higher body temperature, high white cell count in CSF, and deep coma present at hospital admission were markers for unfavorable outcomes (sequelae or fatal). A history of the vaccination was not correlated with the early sequelae and fatal outcome of the disease. The paper suggests that early diagnosis and treatment and universal JE vaccination for all susceptible populations are keys for decreasing incidence of sequelae and fatal outcome of acute JE.     

Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus

The pre- and postnatal findings of a fetus with a de novo del(13)(pter-->q21:) and an occipital encephalocoele are described. Maternal serum alpha-fetoprotein (AFP) screening at 19 weeks' gestation demonstrated a high level of 2.5 multiples of the median (MOM) and ultrasonography at 27 weeks' gestation showed severe intrauterine growth retardation, cardiomegaly, an occipital encephalocoele, and a calvarial defect. Genetic amniocentesis revealed a karyotype of 46,XX,del(13)(pter-->q21:). The proband postnatally displayed additional abnormalities such as microphthalmia, hypertelorism, large low-set ears, and micrognathia. We discuss the association of central nervous system (CNS) malformations with 13q deletions and emphasize that pregnancies with neural tube defects warrant cytogenetic analysis, especially when additional fetal abnormalities and neonatal dysmorphism are observed.