- 更多网络例句与肌肉萎缩相关的网络例句 [注：此内容来源于网络，仅供参考]
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Pertaining to muscular atrophy, as in amyotrophic lateral sclerosis.
与肌肉萎缩退化有关系的，像是肌肉萎缩的侧部硬化。
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MRI characters mainly were that amyotrophy attenuated muscle and muscle outline collapsed;intramuscular adipose heterogeneitily infiltrated,which resulted in MRI signal heterogeneitily raising up and the ratio of lumbar subcutaneous fat MRI signal to lumbar dorsal muscle MRI signal descending;intramuscular spatia was revealed as line-lamellar form or featheriness or grid grid form.
主要MRI表现包括：肌肉萎缩造成肌肉变细、形态萎缩、轮廓萎陷；肌内不均匀性脂肪浸润，造成信号不均性增高，皮下脂肪信号与肌肉信号比值下降，肌内间隙呈线片状、羽毛状或网格状。
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Gene mutations were detected in 25 patients and a 18-year-old girl among 16 families. Trinucleotide repeats of CAG were 73～79. The fragments of abnormal alleles were 380～402bp, and all patients were heterozygous. The copy numbers of normal alleles were 18～40, fragments from 202～270bp. SCV reduction was much obvious compared to MCV, MCV and SCV in lower limb ?ere much more slow than that in upper's. BAEP, VEP were also delayed in latency. The anticipation in parental sex bias were much more obvioius than that in matental's. Cerebellar ataxia was most severe, the next were dysarthria and bulging eyes. Amytrophy was seen only in bed ridden patients. Cerebellar atrophy was more severe than brain stem, cord atrophy was n't observed in all MJD.
结果检出10个家系25例病人及1例症状前18岁女孩有MJD基因突变，CAG三核苷酸重复73～79次，异常等位基因片段长380～402bp，均为杂合子；正常人CAG三核苷酸重复18～40次，等位片段长200～270bp，电生理发现MJD的SCV减慢比MCV明显，而下肢的MCV、SCV又较上肢明显，BAEP、VEP均有不同程度的潜伏期延长或波的异常；MJD的父亲遗传早于母亲，进展也较块，临床以小脑性共济失调为突出症状，其次为构音障碍、突眼等，肌肉萎缩仅见于晚期病人；MRI示小脑萎缩较明显，脑干萎缩并不严重，未见明显的颈髓萎缩。
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There is researcher think, humor can treatment brain two atrophy of hemisphere nerve cell-sloth and weak, positive such as toughen with the athletics can treatment the muscle atrophy similar, if teacher well timed usage teaching humor, cause happiness and dulcify, ability cancellation tired, make the teachers and the students keep spirit to fig up appearance in the whole lesson.
有研究者认为，幽默可以治疗大脑两半球神经细胞的萎缩-惰性和虚弱，正如用体育锻炼可以治疗肌肉萎缩一样，如果教师适时运用教学幽默，引起欢乐和愉悦，则能消除疲劳，使师生在整堂课保持精神振奋状态。
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Limb girdle muscular dystrophy is comprised of a clinically and genetically heterogeneous group of muscle disorders characterized by progressive destruction of the shoulder and hip girdle muscles.
肢带型肌肉失养症是排除目前已知、特异性的退化性肌肉疾病后，一群由表现特徵为渐进式肩带和腰带等近端肌肉无力，以及肌肉萎缩为临床表现的疾病总称。
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Three year old Morgan Bucco is one of thousands of children who are born with rare forms of muscular dystrophy; unlike most, he is part of a unique research project. MS is a wide range of disorders; thus, the research has used a wide, international sample.
三岁的摩根是千分之一中罕见的先天性肌肉萎缩症的小孩，但是不同於其他人的是，他参与了一项很独特的研究计画，肌肉萎缩症包括了范围很广的疾病，因此这项研究使用广泛及国际性的采样。
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This pilot study recruits cases for MUAPs analysis which include normal subjects and representative pathological subjects of progressive muscular dystrophy, polymyositis, and progressive spinal muscular atrophy, one for each case.
本研究在运动单元动作电位分析中，实验对象里有正常人也有明显呈现病徵的患者，包括了渐进性肌肉萎缩、多发性肌炎及渐进性脊髓肌肉萎缩等各一位的患者。
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The degree of atrophy in denervated facial muscle is less than that of denervated extremity.
目的：面部肌肉失神经支配后，其肌肉萎缩同肢体肌肉相比较，萎缩速度慢，病变程度轻。
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Physical therapy to prevent contractures (a condition when an individual with a muscular dystrophy grows and the muscles don't move with the bones and can easily be slowed down and/or make the individual's body straighter by daily physical therapy), orthoses (orthopedic appliances used for support) and corrective orthopedic surgery may be needed to improve the quality of life in some cases.
物理治疗，以防止挛缩（一条件时，个人与肌肉萎缩症的成长和肌肉做不动的骨头和可以很容易地放慢和/或个人的身体直每天物理疗法），矫形器和纠正骨科手术可能需要提高生活质量在某些情况下。。心脏发生的问题与德赖富斯肌肉萎缩症和强直性肌肉营养不良症可能需要一个心脏起搏器。
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Spinal muscular atrophy is the name given to a group of inherited disease characterized by muscle weakness and wasting cause of motor neurones defect.
脊髓性肌肉萎缩症是一群因运动神经元退化而造成肌肉萎缩、无力的遗传性疾病。
- 更多网络解释与肌肉萎缩相关的网络解释 [注：此内容来源于网络，仅供参考]
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amyotrophy：肌肉萎缩
amyotoria 肌弛缓 | amyotrophy 肌肉萎缩 | anabasine 新烟碱
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amyotrophy：肌肉萎缩/肌萎缩
amyotonia /肌弛缓/ | amyotrophy /肌肉萎缩/肌萎缩/ | amytal /阿密妥/安密妥/异戊巴比妥/
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Muscular Dystrophy：肌肉萎缩症
澳洲新南威尔斯大学(the University of New South Wales)的研究人员,在老鼠的研究模式中成功的将干细胞(stem cells)再生为肌肉细胞,对於患有肌肉相关疾病,例如:肌肉萎缩症(muscular dystrophy)的病人,带来治疗上的新希望,
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Muscular Dystrophy：肌肉萎缩
与laminin有缺陷的相关疾病包含肌肉萎缩(muscular dystrophy)和早衰症(progeria). Fibronectin是伤口愈合时第一种形成的醣蛋白,它会与细胞膜上的一种蛋白质受体integrin结合,此外它也会把细胞外的胶原蛋白、纤维素(fibrin)、肝素(heparin)等结合在一起 (可视为卡榫,
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myotonic dystrophy：强直型肌肉萎缩症
其中,位於染色体19q13.3区域内DMPK基因3'端不转译区的此一序列之扩增会造成强直型肌肉萎缩症(myotonic dystrophy). 在此研究中,我们尝试以线虫(C. elegans)作为疾病模式动物来研究强直肌肉萎缩症之可能致病机制. 首先,
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sweeny：肌肉萎缩
Swedish 瑞典人 | sweeny 肌肉萎缩 | sweep all before one 彻底成功
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amyotrophic：肌肉萎缩的
amyotrophic lateral sclerosis 肌肉萎缩性一侧硬化 | amyotrophic 肌肉萎缩的 | amytal interview 阿密妥面谈
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the muscles atrophied：肌肉萎缩了
the ants are in the sugar 蚂蚁成群的在糖罐里 | the muscles atrophied 肌肉萎缩了= = | we're on the other side, the screen is us and we're TV 我们在另一面,我们就是屏幕,我们就是电视
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Her muscles wouldn't have atrophied：解释不了肌肉萎缩
Could be amyloidosis. Amyloid buildup hits the organs,tissue--|可能是淀粉样变性 淀粉堵塞攻击... | Her muscles wouldn't have atrophied.|解释不了肌肉萎缩 | You run the echo on the husband?|你给丈夫做的超声...
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Other spinal muscular atrophies and related syndromes：脊髓性肌肉萎缩,未特指
其他特指的动物传染的细菌性疾病,NEC Other specified zoonotic bacterial diseases... | 其他鞘脂类代谢障碍 Other sphingolipidos... | 脊髓性肌肉萎缩,未特指 Other spinal muscular atrophies and related syndromes