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sutured相关的网络例句

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The proximal and distal nerve stumps were sutured l cm apart, in an end-to-side fashion like "π", to the epneurium windows, opened by removing the epineural sheath on the intact tibial nerve trunk with 1 mm long.

方法将大鼠右侧腓总神经在胭窝处剪除约5mm后,将断裂的腓总神经近端和远端分别就近与同侧胫神经上的外膜窗施行端侧吻合,吻合口间距约10mm;动物存活24个月后,将手术侧近端吻合口以上胫神经剪断,再将辣根过氧化物酶注入远段腓总神经干内,72h后取材并经四甲基联苯胺显色显示脊髓L3-6节段神经元和L4、L5脊神经节细胞,同时取腓总神经远段行电镜观察神经纤维再生状态。

In the side-to-side group, the lateral side of distally severed peroneal nerve trunk with removal of the epineurium was sutured to the tibial nerve trunk with removal of the same area of the epineurium.

侧-侧缝合组:将腓神经远侧断段侧壁去除外膜,同样胫神经侧壁去外膜,两者去除外膜的面积相当于腓神经直径的3倍。

Part three: An experiment study on the repair of peripheral nerve injury by NT-3 gene modified neural stem cells objective To investigate the effective treatment of peripheral nerve injury with NT-3 gene modified neural stem cells, to explore the feasibility of the treatment by means of gene transfection Methods 54 SD rats were divided evenly into 3 groups. The sciatic nerve transected model were made and sutured end to end with epineurium. The neural stem cell without NT-3 gene or with NT-3 gene modified were injected into triceps muscle one time a week, saline injected as control group. The nerve trunks of stomas and triceps muscle were acted as specimen three weeks、six weeks and nine weeks after operation.

最后,为了探讨神经营养素-3基因修饰的神经干细胞对周围神经再生修复的影响,从转基因角度探讨治疗周围神经损伤的有效方法,我们选用54只SD大鼠随机分为3组,造成坐骨神经切断损伤模型,神经外膜端端对位缝合后,于小腿三头肌每周分别注射生理盐水、未被神经营养素-3基因修饰的神经干细胞、及神经营养素-3基因修饰的神经干细胞。

METHODS The animal models of the transected sciatic nerve of 40 SD rats were established, which divided into 4 groups: normal saline group, nerve growth factor group, bFGF group and normal control group. The epineurium of the transected sciatic nerve was sutured under microscope, then bFGF or NGF was dropped into local sites and injected intramuscularly once a day for 30 days after operation.

建立大鼠坐骨神经离断模型,镜下进行神经外膜缝合,局部滴加药物和术后肌注bFGF 以及临床用药神经生长因子,通过神经传导速度和功能指数评定观察坐骨神经修复情况。

Methods The animal models of the transected sciatic nerve of 40 SD rats were established, which divided into 4 groups:normal saline group, nerve growth factor group,bFGF group and normal control group. The epineurium of the transected sciate nerve was sutured under microscope, then bFGF or NGF was dropped into local sites and injected intramuscularly once a day for 30 days after operation.

建立大鼠坐骨神经离断模型,镜下进行神经外膜缝合,局部滴加药物和术后肌注bFGF以及临床用药神经生长因子,通过神经传导速度和功能指数评定观察坐骨神经修复情况。

Methods: 60 Wistar rats were randomly divided into three groups, with 20 rats each. The right radial nerve was repaired with end-to-side fashion after windowed, the distal end being sutured to the epineurial window (0.12 cm×0.12 cm) 0.15 cm distal of the medial fasciculus. The left radial nerve was only windowed as control.

Wistar大鼠60只,随机分为3组,每组20只,每只右侧神经外膜开窗(0.12 cm×0.12 cm),将臂丛后束损伤后的桡神经远断端端侧吻合于外膜开窗的内侧束远端0.15 cm部位,左侧不做吻合。

The diseased lung tissues were serially ligated with the Roeders knot and the hilum of the lung tightly locked with a Rumel's hemostat. The raw surface of the resected lung was sutured.

术中采用Roeder结套扎肺组织或创用Rumel止血器锁紧肺根部、腔镜下缝合肺残端创面等方法处理病肺。

The incision need not to be sutured. Results: A total of 24 cases have undergone the operation.

结果:24例患者接受了这种方法的手术,效果满意。

Thirdly, the impaired volar capsular l igament complex was interruptedly sutured by the use of 4# suture silk.

呈弧形切断掌侧关节囊韧带复合体;用4 号丝线间断缝合关节囊韧带;模拟临床操作外固定支架

In the EPC repair group, 1010/L passage 3 rabbit bone marrow mononuclear cell suspension was injected to two anastomotic stomas of the new urethra, 0.1 mL for each stoma. The subcutaneous tissue was interruptedly sutured to the formed urethra using 0/6 DG suture. In addition, 0.5 mL bone marrow mononuclear cell suspension was added to the region between each anastomotic stroma and newly repaired urethra. The same procedure was performed in the model group except that bone marrow mononuclear cell suspension was replaced by cell-free medium.

细胞修复组将传至第3代的兔骨髓源单个核细胞浓度调整至1010 L-1,注射于新尿道两端的吻合口处,每处0.1 mL,0/6DG线间断缝合皮下组织覆盖成形后的尿道,并在近吻合口处和新修复尿道之中间处注射细胞悬液,每处0.5 mL;模型组在同样位点注射等量的空白细胞培养液。

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