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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(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。
- 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。
- 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。
- Objective To investigate the clinical features, diagnosis and differential diagnosis of progressive spinal muscular atrophy (PSMA). 摘要目的探討進(jìn)行性脊肌萎縮癥(PSMA)的臨床特點(diǎn)、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(dòng)物模式探討干細胞治療;中風(fēng);急性腎衰竭;人類(lèi)脊髓肌肉萎縮癥分子機制.
- 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(shù)前有明顯肌萎縮者未見(jiàn)恢復外,其余22例術(shù)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(jìn)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癥患兒的臨床及電生理表現，探討本病的電生理特點(diǎn)及早期診斷要點(diǎn)。
