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- Muscular atrophy of a person affected with paralysis. 因麻痹而導致人體肌肉萎縮
- Individual local myasthenia gravis patients, muscular atrophy. 個別患者出現局部肌無力、肌萎縮。
- A gene implicated in Spinal Muscular Atrophy showed an association in three populations, but not in Yoruba from Ibadan, Nigeria. 一個涉及脊髓性肌萎縮病的基因顯示出與三個人群有關聯但卻沒有在伊巴丹、奈及利亞、的優魯巴人身上發現。
- Clinical, electromyography (EMG) and nerve conduction velocity (NCV) features of 32 cases with peroneal muscular atrophy (PMA) are reported. 本文報告32例腓骨肌萎縮症(PMA)患者的臨床及肌電圖(EMG)和神經傳導速度(NCV)的改變。
- With toe (HSI) A slow growth, thickening deformation, dry skin thinning, Ganmao exfoliated and muscular atrophy. 伴趾(指)甲生長緩慢，增厚變形，皮膚乾燥變薄，汗毛脫落和肌肉萎縮。
- Two cases of shoulder petoneal muscular atrophy (SPMA),a rare type of charcot-Marie- Tooth disease,are reported. 本文報告兩例進行性神經性肌萎縮症(Charcot-Marie-Tooth)的少見特殊類型-肩胛腓骨萎縮型,亦屬慢性遺傳性進行性周圍神經病的變異型之一。
- Objective To study survival motor neuron (SMN) deletion in adult-onset patients with spinal muscular atrophy (SMA). 目的探討成年起病的脊肌萎縮症(SMA)患者的運動神經元存活基因SMN的缺失情況。
- Objective To establish a gene diagnosis assay for spinal muscular atrophy(SMA) in children. 目的探討兒童脊髓性肌萎縮症(SMA)的特異性基因診斷方法。
- Objective: To establish a genetic diagnosis assay for spinal muscular atrophy (SMA) in children. 摘要目的：建立兒童型脊髓性肌萎縮症(SMA)的特異性基因診斷平台。
- The double lower limb cannot walk, has not seen the ischemic muscular atrophy and the myodynamia is not normal. 雙下肢不能行走，未見肌肉萎縮和肌力不正常。
- Inspect the patient's hands and wrists, noting any swelling, redness, nodules, deformities, or muscular atrophy. 仔細觀察病人的手和手腕，注意有沒有腫塊，紅點，小瘤，畸形，肌肉萎縮等癥狀
- ObjectiveTo establish spinal muscular atrophy (SMA) cell model by blocking the expression of SMN1 gene with shRNA. 目的：應用RNA干擾沉默SMN1基因的表達建立脊髓性肌萎縮症（SMA）的細胞模型。
- Objective To carry out prenatal gene diagnosis in a pedigree of infantile spinal muscular atrophy (SMA). 目的對一嬰兒型脊肌萎縮症家系進行產前基因診斷。
- Objective This study examined the prevalence of deletion and subtle mutations of survival motor neuron( SMN) gene in children with spinal muscular atrophy( SMA). 目的研究兒童型脊肌萎縮症(MA)者中運動神經元生存基因缺失與微突變情況。
- Objective To investigate the relationship between survival motor neuron(SMN)gene and the clinical features of childhood spinal muscular atrophy(SMA). 目的探討運動神經元存活基因與兒童期脊肌萎縮症臨床特徵的關係。
- Objective To investigate the clinical features, diagnosis and differential diagnosis of progressive spinal muscular atrophy (PSMA). 摘要目的探討進行性脊肌萎縮症(PSMA)的臨床特點、診斷與鑒別診斷。
- Study mechanism of the stem cell therapy, stroke, acute renal failure, and spinal muscular atrophy by transgenic and knockout mice. 利用小鼠動物模式探討幹細胞治療;中風;急性腎衰竭;人類脊髓肌肉萎縮症分子機制.
- Results 22 cases were improved obviously from nerves entrapment syndrome except 2 failure with severe muscular atrophy before the treatment. 結果除2例術前有明顯肌萎縮者未見恢復外,其餘22例術后癥狀均得到明顯改善。
- Results The CT features involved mainly muscular atrophy, hypo - density, selective involvement, muscular hypertrophy and pseudohypertrophy. 對其骨骼肌的CT表現進行了對照分析。
- Objective To explore the feature of electrical physiology and the key aspect of diagnosis in early stage of spinal muscular atrophy in infants. 摘要目的分析嬰兒型脊肌萎縮症患兒的臨床及電生理表現，探討本病的電生理特點及早期診斷要點。
