- 更多网络例句与肌性膜性的相关的网络例句 [注：此内容来源于网络，仅供参考]
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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。
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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。
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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。
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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。
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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。
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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。
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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。
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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。
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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。
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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。
- 更多网络解释与肌性膜性的相关的网络解释 [注：此内容来源于网络，仅供参考]
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actomyosin：肌动凝蛋白
胞膜中肌动凝蛋白(actomyosin)由溶胶变为凝胶,因而红细胞膜变僵硬,丧失柔韧性. 球形细胞的直径虽然小于6μ左右,但由于细胞膜变形性和柔韧性减退而被阻留在脾索内,不能通过内皮细胞间空隙(直径仅为3μ左右)进入脾窦. 大量红细胞在脾索内滞留过程中,
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cardiac muscle：心肌
肌纤维的细胞膜称肌膜(sarcolemma),细胞质称肌浆(sar二、心肌 心肌(cardiac muscle)分布于心脏和邻近心脏的大血管近段. 心肌收缩具有自动节律性,缓慢而持久,不易疲劳. (一)心肌纤维的光镜结构 心肌纤维呈短柱状,多数有分支,相互连接成网状.
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episcleritis：鞏膜炎
表层巩膜炎(episcleritis)是巩膜表层(或浅层)组织的炎症,多位于角膜缘至直肌附着线之间赤道前部. 有周期发作的病史,愈后不留痕迹. 成年男女皆可患病,但女性较多见,多数患者为单眼发病. 原因常不明,多见于外原性抗原抗体所致的过敏原性反应,
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FAB：抗原结合片段
重症肌无力是由抗乙酰胆碱受体抗体介导的自身免疫病,而致病性抗乙酰胆碱受体抗体多为IgG类抗体,它的2个抗原结合片段(Fab)与神经肌肉接头处突触后膜上相邻的2个乙酰胆碱受体结合,可加快乙酰胆碱受体的内化作用(即抗原调变);
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Inactivation：失活
离子通道都有备用(或称静息resting)、激活(activation)和失活(inactivation)三种状态. 通道处于何种状态,取决于大家学习网原 创当时的膜电位水平和在该电位的时间进程(即电压依从性和时间依从性). 心肌工作肌胞是快反应细胞,
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inspiratory capacity：深吸气量
顺应性是指在外力作用下弹性组织的可扩张性,容易扩张的顺应性(C)大,弹性阻力(R)小. 1.深吸气量(inspiratory capacity) 是衡量最大通气潜力的一个重要指示. 胸廓、膜、肺组织和呼吸肌等的病变时减少.
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desmoid tumor：韧带状瘤
<正> 本病又称韧带状瘤(desmoid tumor)或侵袭性纤维瘤病(aggressive fibromatosis),是介于良恶性之间的纤维性肿瘤. 其特点为纤维组织的增生并形成瘤样病变,增生的纤维组织较为成熟,与纤维瘤相似,但无包膜. 病变源自肌筋膜,常呈浸润性生长,
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epinaos：后室
epimysium 肌外膜 | epinaos 后室 | epinastic 偏上性的
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isotropism：各向同性
横纹肌(骨骼肌和心肌)肌原纤维的肌小节的明亮部分. 它和暗的A带交互并列而形成横纹,中央部分由Z膜隔开. I带在肌肉松弛时变宽,收缩时可变窄. 这是因为I带中的I细丝向A带中的A细丝之间滑行所致. 与A带相比,I带的双折射性弱,因此有所谓各向同性(isotropism)的命名(恩格尔曼(W.T.Engelmann),1873).
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neurogenic：神经性
但是科学一点, 根据年纪的分类, 可以分成先天(congenital)和后天(acquired, 又称为年老性--Senile)两类; 倘若依据病因(etiology), 可以分成肌肉性(myogenic, 如重症肌无力), 神经性(neurogenic), 筋膜性(aponeurotic),