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- Clinical, electromyography (EMG) and nerve conduction velocity (NCV) features of 32 cases with peroneal muscular atrophy (PMA) are reported. 本文報告32例腓骨肌萎縮癥(PMA)患者的臨床及肌電圖(EMG)和神經(jīng)傳導速度(NCV)的改變。
- progressive neuropathic peroneal muscular atrophy 進(jìn)行性神經(jīng)病性腓肌萎縮
- progressive peroneal muscular atrophy 進(jìn)行性腓骨肌萎縮
- Inherited neuronal peroneal muscular atrophy 遺傳性神經(jīng)性腓側肌萎縮
- peroneal muscular atrophy 腓側肌萎縮, 腓肌萎縮
- According to the involved area and illness course, MND can be divided into several types, but amyotrophic lateral sclerosis(ALS) and progressive muscular atrophy(PMA) are the main types. 根據病變累及部位及病程可分為許多類(lèi)型，其中最主要的有肌萎縮側索硬化（Amyotrophic lateralsclerosis，ALS）和進(jìn)行性脊肌萎縮癥（Progressive muscular atrophy，PMA）。
- 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(gè)別患者出現局部肌無(wú)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(gè)涉及脊髓性肌萎縮病的基因顯示出與三個(gè)人群有關(guān)聯(lián)但卻沒(méi)有在伊巴丹、尼日利亞、的優(yōu)魯巴人身上發(fā)現。
- With toe (HSI) A slow growth, thickening deformation, dry skin thinning, Ganmao exfoliated and muscular atrophy. 伴趾(指)甲生長(cháng)緩慢，增厚變形，皮膚干燥變薄，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(jìn)行性神經(jīng)性肌萎縮癥(Charcot-Marie-Tooth)的少見(jiàn)特殊類(lèi)型-肩胛腓骨萎縮型,亦屬慢性遺傳性進(jìn)行性周?chē)窠?jīng)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癥(SMA)患者的運動(dòng)神經(jīng)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癥(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癥(SMA)的特異性基因診斷平臺。
- 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(jiàn)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(guān)察病人的手和手腕，注意有沒(méi)有腫塊，紅點(diǎn)，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癥（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癥家系進(jìn)行產(chǎn)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?jì)和图辜∥s癥(MA)者中運動(dòng)神經(jīng)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(dòng)神經(jīng)元存活基因與兒童期脊肌萎縮癥臨床特征的關(guān)系。
