肌性膜性的

Hirayama disease should be considered for young patient,especially male patient,with asymmetrical amyasthenia and amyotrophy in the hand and forearm.Hirayama disease can be diagnosed if MR abnormalities of the lower cervical dural sac and spinal cord are seen in a fully flexed position.

当遇到青少年出现手及前臂不对称的肌无力和萎缩而无感觉障碍时，应首先考虑有平山病的可能，可进一步行屈颈MR检查，出现下颈髓及其硬膜囊的特征性表现可确诊。

The pathological diagnosis should include:(1) the electromyographic recording and ultrasound imaging of local twitch responses,(2) the EMG recording of spontaneous electrical activity at multiple active loci in the MTrP, and (3) the biopsies of MTrP that show contraction knots and giant round muscle fibers.

病理学的诊断应该包括：(1)局部抽搐反应的肌电图记录与超音波影像，(2)在肌筋膜激痛点里的多发性活动性小点上之自发性电位活动的肌电图纪录，(3)肌筋膜激痛点的切片检查显现出收缩结节和大而圆的肌肉纤维。

Results: MC of tryptase immunoreactivity contain abundant F-actin ring that region of cytomembrane endothecium form a barrier of blocking tryptase liberation. Copious tryptase temporarily was stored in secretory vacuole, and small amounts tryptase was released from secretory vacuole for depolymerize of F-actin ring in cell.

结果：类胰蛋白酶免疫反应性的肥大细胞内含有丰富的丝状肌动蛋白环，在质膜内层区域形成阻碍类胰蛋白酶释放的屏障；大量的类胰蛋白酶暂存于分泌泡中，少量的类胰蛋白酶因细胞内丝状肌动蛋白环的解聚使之从分泌泡中释放。

Results: MC of tryptase immunoreactivity MC(subscript T contain abundant F-actin ring that region of cytomembrane endothecium form a barrier of blocking tryptase liberation. Copious tryptase was temporarily stored in secretory vacuole, and small amounts of tryptase was released from secretory vacuole for depolymerize of F-actin ring in cell.

结果：类胰蛋白酶免疫反应性的肥大细胞内含有丰富的丝状肌动蛋白环，在质膜内层区域形成阻碍类胰蛋白酶释放的屏障；大量的类胰蛋白酶暂存于分泌泡中，少量的类胰蛋白酶因细胞内丝状肌动蛋白环的解聚使之从分泌泡中释放。

Results These two patients were confirmed to suffer from DMD. They were characterized by typical features of DMD including typical clinical manifestations, increased serum enzymes, EMG presenting myogenic impairment, HE staining presentation belonging to DMD, negative dystrophin in brother, and inconstantly positive on the sarcolemma of sister. Furthermore, no deletion or duplication was found in the 1-79 exons of dystrophin gene. The suffering brother and sister carried the same maternal X chromosome.

结果 兄妹二人符合DMD诊断，具有典型的DMD临床表现，肌酸激酶、肌酸激酶同工酶、乳酸脱氢酶、羟丁酸脱氢酶和谷草转氨酶的水平均显著高于正常值，肌电图呈肌源性损害，肌肉HE染色符合DMD，男患者的抗肌萎缩蛋白表达阴性，女患者的少量肌纤维仍可见不连续膜阳性，两患者抗肌萎缩蛋白基因的1~79号外显子未见缺失和重复突变，女患者与男患者携带相同的母源性X染色体。

CK, LDH in serum, SOD, MDA in muscular tissue, and Na+-K+-ATPase activity in sarcolemma were measured respectively.

以DPH和N[3P]M为探针，用荧光分光光度计分别测定肌细胞膜脂质流动性和膜蛋白的活动性。

Bicepts femoris dry matter are 9240.16 ug nonane 100g-1 and 13227.85 ug nonane 100g-1 respectively at 6 months. Aldehydes are primary compounds in process of Xuanwei ham, in which the tiptop content is 6744.60 ug nonane 100g-1 and 11326.18 ug nonane 100g-1 in M. semimembranosus and M. Bicepts femoris dry matter at 6 months, and then drops.

醛类是每个加工阶段种类最多、含量最丰富的挥发性化合物，在6个月时的总含量达到最高值半膜肌和股二头肌干物质中的含量分别为6744.60 μg壬烷·100g~(-1和11326.18μg壬烷·100g~(-1)，随后含量下降。

Methods: Tissue of rat ovary was obtained from 30 healthy sexually mature non-mated femal SD rats. The rats were divided into two groups (oestrus group and anoestrus group). The expression of α-SMA and vimentin were detected and evaluated by immunohistochemistry and image analysis system in the theca cells of different type follicles.

分别取动情期和非动情期大鼠卵巢，运用免疫组化方法检测肌成纤维细胞的特征性标记和波形蛋白分别在这两组中各级卵泡卵泡膜细胞上的表达情况，并进行图像分析。

An MTrP is a hyperirritable spot in a taut band of skeletal muscle fibers with characteristics related to central sensitization in the spinal cord.

肌筋膜激痛点是骨骼肌肉纤维里紧绷肌带上的过度激活点，伴随著与脊髓里中枢性敏感化有相关联的特徵。

In this review data on the use of rituximab is presented from 92 studies involving 1197 patients with the following diseases: systemic lupus erythematosus, idiopathic thrombocytopenic purpura, anti-neutrophil cytoplasmic antibody associated vasculitis, Grave's disease, autoimmune hemolytic anemia, pemphigus vulgaris, hemophilia A, cold agglutinin disease, Sjogren's syndrome, graft vs. host disease, thrombotic thrombocytopenic purpura, cryoglobulinemia, IgM mediated neuropathy, multiple sclerosis, neuromyelitis optica, idiopathic membranous nephropathy, dermatomyositis, and opsoclonus myoclonus.

本综述资料总结了92项共1197例患者应用利妥昔的研究，包括系统性红斑狼疮、特发性血栓性血小板减少性紫癜，抗中性粒细胞抗体相关性血管炎、甲状腺功能亢进、自身免疫性溶血性贫血、寻常型天疱疮、甲型血友病、冷凝集素病、干燥综合征、移植抗宿主疾病、血栓性血小板减少性紫癜、IgM介导性神经病、多发性硬化、视神经脊髓炎、特发性膜性肾病、皮肌炎和眼肌阵挛性肌阵挛。

Neither the killing of Mr Zarqawi nor any breakthrough on the political front will stop the insurgency and the fratricidal murders in their tracks.

在对危险的南部地区访问时，他斥责什叶派民兵领导人对中央集权的挑衅行为。

In fact,I've got him on the satellite mobile right now.

实际上 我们已接通卫星可视电话了