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- progresive muscular atrophy 克律韦利埃氏麻痹
- Muscular atrophy of a person affected with paralysis. 因麻痹而导致人体肌肉萎缩
- Individual local myasthenia gravis patients, muscular atrophy. 个别患者出现局部肌无力、肌萎缩。
- A gene implicated in Spinal Muscular Atrophy showed an association in three populations, but not in Yoruba from Ibadan, Nigeria. 一个涉及脊髓性肌萎缩病的基因显示出与三个人群有关联但却没有在伊巴丹、尼日利亚、的优鲁巴人身上发现。
- Clinical, electromyography (EMG) and nerve conduction velocity (NCV) features of 32 cases with peroneal muscular atrophy (PMA) are reported. 本文报告32例腓骨肌萎缩症(PMA)患者的临床及肌电图(EMG)和神经传导速度(NCV)的改变。
- With toe (HSI) A slow growth, thickening deformation, dry skin thinning, Ganmao exfoliated and muscular atrophy. 伴趾(指)甲生长缓慢，增厚变形，皮肤干燥变薄，汗毛脱落和肌肉萎缩。
- Two cases of shoulder petoneal muscular atrophy (SPMA),a rare type of charcot-Marie- Tooth disease,are reported. 本文报告两例进行性神经性肌萎缩症(Charcot-Marie-Tooth)的少见特殊类型-肩胛腓骨萎缩型,亦属慢性遗传性进行性周围神经病的变异型之一。
- Objective To study survival motor neuron (SMN) deletion in adult-onset patients with spinal muscular atrophy (SMA). 目的探讨成年起病的脊肌萎缩症(SMA)患者的运动神经元存活基因SMN的缺失情况。
- Objective To establish a gene diagnosis assay for spinal muscular atrophy(SMA) in children. 目的探讨儿童脊髓性肌萎缩症(SMA)的特异性基因诊断方法。
- Objective: To establish a genetic diagnosis assay for spinal muscular atrophy (SMA) in children. 摘要目的：建立儿童型脊髓性肌萎缩症(SMA)的特异性基因诊断平台。
- The double lower limb cannot walk, has not seen the ischemic muscular atrophy and the myodynamia is not normal. 双下肢不能行走，未见肌肉萎缩和肌力不正常。
- Inspect the patient's hands and wrists, noting any swelling, redness, nodules, deformities, or muscular atrophy. 仔细观察病人的手和手腕，注意有没有肿块，红点，小瘤，畸形，肌肉萎缩等症状
- ObjectiveTo establish spinal muscular atrophy (SMA) cell model by blocking the expression of SMN1 gene with shRNA. 目的：应用RNA干扰沉默SMN1基因的表达建立脊髓性肌萎缩症（SMA）的细胞模型。
- Objective To carry out prenatal gene diagnosis in a pedigree of infantile spinal muscular atrophy (SMA). 目的对一婴儿型脊肌萎缩症家系进行产前基因诊断。
- Objective This study examined the prevalence of deletion and subtle mutations of survival motor neuron( SMN) gene in children with spinal muscular atrophy( SMA). 目的研究儿童型脊肌萎缩症(MA)者中运动神经元生存基因缺失与微突变情况。
- Objective To investigate the relationship between survival motor neuron(SMN)gene and the clinical features of childhood spinal muscular atrophy(SMA). 目的探讨运动神经元存活基因与儿童期脊肌萎缩症临床特征的关系。
- Objective To investigate the clinical features, diagnosis and differential diagnosis of progressive spinal muscular atrophy (PSMA). 摘要目的探讨进行性脊肌萎缩症(PSMA)的临床特点、诊断与鉴别诊断。
- Study mechanism of the stem cell therapy, stroke, acute renal failure, and spinal muscular atrophy by transgenic and knockout mice. 利用小鼠动物模式探讨干细胞治疗;中风;急性肾衰竭;人类脊髓肌肉萎缩症分子机制.
- Results 22 cases were improved obviously from nerves entrapment syndrome except 2 failure with severe muscular atrophy before the treatment. 结果除2例术前有明显肌萎缩者未见恢复外,其余22例术后症状均得到明显改善。
- Results The CT features involved mainly muscular atrophy, hypo - density, selective involvement, muscular hypertrophy and pseudohypertrophy. 对其骨骼肌的CT表现进行了对照分析。
