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1.
肿瘤微波热疗的温度场预示及热损伤研究   总被引:2,自引:0,他引:2  
本文将热损伤的产生和影响引入到肿瘤的微波热疗中。运用微波能量比吸收率SAR的分布分析了微波在组织中的传输和吸收过程,并对微波热疗过程中的温度场、热损伤分布以及血液灌注率的变化进行了数值模拟。  相似文献   
2.
对西安地区150例0~3岁儿童进行了六种微量元素:钙、锌、铜、铁、镁、硒的检测,发现微量元素缺乏可导致急慢性感染、免疫力低下、小儿营养不良、贫血、发育迟缓等症状。并对小儿营养不良、喂养不当进行矫正。其中铁、钙、锌同时缺乏占50%。  相似文献   
3.
Several studies have reported prevalence rates for voice disorders in school-aged children. Less is known, however, about such prevalence in preschoolers, and whether racial, ethnic, or cultural diversity may influence it. The presence of voice disorders in a total of 2445 African-American and European-American preschool children, 1246 males and 1199 females, from 2 to 6 years of age is reported here. Presence of a voice disorder characterized by hoarseness was identified by a three-prong approach including teacher identification, investigator screening, and parent identification. Speech-language pathologists listened individually to each child's speech as they engaged each child in play-conversation activities. A voice disorder was identified on the basis of the judgment of two speech-language pathologists. Voice disorders characterized by hoarseness were identified in 95 children or 3.9% of the total sample by the investigators. Statistical analysis revealed no significant differences for age, gender, or race.  相似文献   
4.
526例儿童指血微量元素检测结果分析   总被引:8,自引:0,他引:8  
为了解吐哈油区婴幼儿体内钙、铁、锌、铜、镁的含量,使用多通道原子吸收光谱仪对门诊体查的526例0~7岁幼儿指血检测了钙、铁、锌、铜、镁。结果表明,各个年龄组中缺铁均居第一位,缺钙居第二位,缺锌居第三位,年龄越小,这3种元素含量越低。提示婴幼儿生长发育快,易缺钙,铁,锌元素,年龄越小,越易缺乏。  相似文献   
5.
为了解最近5年广州医学院港湾医院辖区内0~6岁小儿的营养、健康状况变化趋势和明确今后儿童保健工作的重点,对该院管辖的7所幼儿园集体儿童及9个居委散居儿童,连续5年(2002—2006年)的体检资料进行了回顾性分析,人数达14485人,所有的体检资料均按照《WHO 0~6岁儿童身高体质量参考值及评价标准》以及贫血、视力异常、龋齿的国家卫生部标准进行评价。结果表明,总体的儿童营养不良率为0.86%,肥胖率为1.87%,生长迟缓患病率为1.26%,轻度贫血率1.35%;观察各年情况,肥胖率有逐年增长趋势,儿童营养不良率无逐年下降趋势;广州医学院港湾医院辖区内0~6岁小儿的营养不良、肥胖、生长迟缓、轻度贫血等患病率低于全国水平,但也有不容忽视之处,营养不良、轻度贫血等并没有因生活水平的提高而消失。加强对家长的科学育儿健康教育,以提高他们的育儿知识水平,是儿保工作的重点,应进一步降低儿童营养不良、贫血的发生率;对儿童肥胖应当切实采取措施,预防和控制肥胖症的发生。  相似文献   
6.
为探讨低锌对儿童反复呼吸道感染的影响 ,检测了 1 2 3例儿童指血锌 (Zn)值 ,并采用t检验 ,与正常儿童组进行血锌值比较。结果表明 ,反复呼吸道感染组血Zn值 48 69± 4 89μmol/L ,正常儿童组血Zn值 5 7 46± 1 9 1 8μmol/L ,经t检验 ,t>t0 0 1( 12 1) ,P <0 0 1 ,具有极其显著差异。提示儿童锌缺乏明显导致儿童免疫力下降 ,削弱机体对病毒及细菌的抵抗力 ,适当补锌有助于预防和治疗上呼吸道感染  相似文献   
7.
贾常明 《大学物理》2008,27(5):41-43
通过建立力学模型,分析轿车冲撞行人的力学过程,对此进行了计算和讨论,进而得到与实验结果相吻合的使行人发生倒立时轿车车速的临界值.并提供了一种有效估算临界车速的方法.  相似文献   
8.
Excessive inflammatory reaction aggravates brain injury and hinders the recovery of neural function in nervous system diseases. Microglia, as the major players of neuroinflammation, control the progress of the disease. There is an urgent need for effective non-invasive therapy to treat neuroinflammation mediated by microglia. However, the lack of specificity of anti-inflammatory agents and insufficient drug dose penetrating into the brain lesion area are the main problems. Here, we evaluated a series of calixarenes and found that among them the self-assembling architecture of amphiphilic sulfonatocalix[8]arene (SC8A12C) had the most potent ability to suppress neuroinflammation in vitro and in vivo. Moreover, SC8A12C assemblies were internalized into microglia through macropinocytosis. In addition, after applying the SC8A12C assemblies to the exposed brain tissue, we observed that SC8A12C assemblies penetrated into the brain parenchyma and eliminated the inflammatory factor storm, thereby restoring neurobiological functions in a mouse model of traumatic brain injury.  相似文献   
9.
A simple, novel, specific, rapid and reproducible ultra‐performance liquid chromatography electrospray ionization tandem mass spectrometry method has been developed and validated for the determination of hydroxysafflor yellow A (HSYA) in biological fluids (plasma, urine and cerebrospinal fluid) of patients with traumatic brain injury after intravenous injection of Xuebijing (XBJ). Liquid–liquid extraction was performed, and separation was carried out on an Acquity UPLC? BEH C18 column, with gradient elution using a mobile phase composed of methanol and 0.1% formic acid at a flow rate of 0.3 mL/min. A triple quadrupole tandem mass spectrometer with electrospray ionization was used for the detection of HSYA. The mass transition followed was m/z 611.0 → 491. The retention time was less than 3.0 min. The calibration curve was linear in the concentration range from 2 to 6125 ng/mL for cerebrospinal fluid, plasma and urine. The intra‐ and inter‐day precisions were <10%, and the relative standard deviation of recovery was <15% for HSYA in biological matrices. The method was successfully applied for the first time to quantify HSYA in the biological fluids (especially in cerebrospinal fluid) of patients with traumatic brain injury following intravenous administration of XBJ. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
10.
Urinary d ‐lactate is highly correlated to diabetic nephropathy – a progressive kidney disease in renal glomeruli. In this study, we used a C3H/3e mouse model to investigate the relationship between urinary d ‐lactate and aristolochic acid nephropathy where the glomerular structure is not affected. The nephropathy was induced using intravenous injections of aristolochic acid at a dosage of 10 mg/kg per day for 5 days and was characterized biochemically and histologically. The urinary excretions of proteins, N‐acetyl‐β‐d ‐glucosaminidase and serum creatinine were determined and connected to histological conventional findings. Urinary d ‐lactate was analyzed using column‐switching high‐performance liquid chromatography with fluorescence detection. The results showed a remarkable increase of urinary markers, including of urinary proteins and N‐acetyl‐β‐d ‐glucosaminidase, and the histological examination confirmed a diagnosis of acute tubule necrosis. The ratio of d ‐lactate to creatinine in the urine of aristolochic acid‐treated mice was approximately 36 times greater than that of the mice in the control group (p < 0.05). The ratios for the two groups of mice were 311.00 ± 71.70 and 8.60 ± 1.80 µmol/mmol creatinine, respectively. These data confirm in vivo that urinary d ‐lactate reflects renal injury conditions in aristolochic acid‐treated mice and may be a marker for the assessment of nephropathy. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
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