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Then the brains were sectioned at 40 u m on a freezing microtome, and stained with neutral red. Histological sections were examined microscopically.

然后冰冻切片,厚度为40 μm,制成标本,中性红染色,用光学显微镜检查刺激电极位置,与图谱对照,刺激位点不在刺激目标核团内的样本舍弃。

This examination is performed by dropping oil on the periungual area and examining with an ophthalmoscope set at diopter 40, or with a dissecting microscope.

进行这项检查需在甲周点滴油,用屈光度为40的眼底镜,或用解剖显微镜进行检查。

A corneal abrasion with a diameter of 7 mm was created centrally in both eyes with a trephine and subsequent rubbing off on the corneal epithelium with a 20% alcohol soaked swab. Photographic documentation and hematoxylin and eosin stained pathological section were performed when rabbits were killed at 0,12,24,36,48 and 72 h. Planimetry was performed, and the corneal photographs were analyzed with computer software.

将4组兔双眼角膜中央置入直径7.00mm的环钻,其内滴入20%乙醇约60s后用角膜刮匙刮去角膜上皮,制作角膜上皮缺损模型,术后每组滴用眼液频率均为3次/d,各组分别于术后12,24,36,48及72h行裂隙灯下荧光素染色照相及海德堡共焦激光角膜显微镜检查后各处死2只兔,取角膜做病理切片同时应用计算机图像处理系统测量角膜损伤后愈合面积。

Methods In vivo confocal microscopy was performed on 52 patients of suspected fungal keratitis,the results were compared with the culture of corneal scrapings.

用共焦显微镜对5 2例临床拟诊为真菌性角膜炎的患者进行检查,同时行角膜病灶刮片培养,对两组结果进行比较。

All rats were confirmed that no anterior segment disease before the experiment with slit lamp microscope examination.

材料:健康SD大鼠60只,体质量180~210 g,鼠龄6~8周,雌雄各半,实验前用裂隙灯显微镜检查证实无眼前段病变。

15 patients of daily soft contact lens wearers and 11 control subjects who had never worn contact lens, were examined by laser confocal microscopy, compare the results of two groups.

方法用激光共焦显微镜对长期佩戴角膜软性接触镜的15例患者进行检查,并选择未戴角膜接触镜者11例进行对照,对两组结果进行比较。

There were inflammatory cells infiltrating in the myocardium sparely and no calcification in the pericardium in IVIG and IVIG+VitC groups. The size of spleens enlarged especially in IVIG and IVIG+VitC groups.

心脏分为三部分:一部分作病理切片和H-E染色,一部分作冰冻切片,在荧光显微镜下用直接免疫荧光法测定心肌组织中沉积的IgG水平,一部分作电镜检查。

Stool samples were examined microscopically for the presence of parasite.

用显微镜检查粪便中的肠道寄生虫。

We observed the changes of the proprioceptors in the partly injuried ACL and the xenogeneic graft/artificial graft being used to reconstructing the injuried ACL with gold chlorid staining method and laser copolymerization electron micrography method to observe the morphological changes of the neuromechanism in the ligament tissue,with RT-PCR method to evaluate the proportion and the regeneration of the nerve component and with HRP retrograde tracking technology and electrophysiologic study to judge the functional changes of the neuromechanism in the ligament tissue,respectively.

本研究分别制作兔ACL部分损伤动物模型、异种肌腱移植物重建损伤ACL动物模型和LARS人工韧带重建损伤ACL动物模型,分别于术后不同时间点对损伤ACL/移植物进行氯化金染色光学显微镜检查和PGP9.5免疫荧光染色后激光共聚焦电子显微镜检查观察韧带内神经结构形态学变化,用RT-PCR法检测韧带中GAP-43和PGP 9.5的mRNA表达情况以评价损伤ACL/移植物内神经成分比例及神经再生情况,通过HRP逆行追踪技术和电生理检查(包括体感诱发电位和腘绳肌肌电图)评价损伤ACL/移植物内神经结构的功能情况。

Under microscopic examination, there were similar spicules on the exocuticle of the tarantula's exuvia. The tarantula was identified as Grammostola rosea.

用显微镜进一步检查蜘蛛的脱壳,可在其体壁上发现类似的结构经鉴定确认此蜘蛛为Grammostola rosea。

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