肌神經萎縮 的英文怎麼說

中文拼音 [jīshénjīngwēisuō]
肌神經萎縮 英文
neuromuscular atrophy
  • 肌 : 名詞1. （肌肉） muscle; flesh 2. [書面語] （皮膚） skin
  • 神 : Ⅰ名詞1 （神靈） god; deity; divinity 2 （精神; 精力） spirit; mind 3 （神氣; 神情） expression; l...
  • 經 : 經動詞[紡織] （把紡好的紗或線梳整成經紗或經線） warp
  • 萎 : 萎動詞（衰落） decline; wane
  • 縮 : 縮構詞成分。
  • 神經 : nerve; nervus
  • 萎縮 : 1 （乾枯） wither; shrivel 2 （經濟衰退） shrink; sag; contraction3 [醫學] depauperate; analosis;...
  1. What is neuromuscular disease and muscular dystrophy

    什麼是神經肌肉疾病和肌肉萎縮癥？
  2. The product is also used for hepatopathy anaemia, poisoning, sweeny, poliomyelitis, and psychopathy

    伴有膽汁分泌減少的肝病、貧血、中毒、肌萎縮癥、脊髓灰質炎后遺癥、神經及精神病。
  3. Elevation of intracellular calcium ions may be partly induced by increased influx through sarcolemma l type - calcium channels. intracellular calcium elevation, on one hand, would activate calpain, a calcium - dependent cysteine protease that degrade the myofibrillar proteins and cause muscle atrophy ; on the other hand, result in activation of calcineurin which enhance the activity of mhc i promoter and inhibit a shift of mhc isoforms from slow to fast in soleus

    這樣，可能使得萎縮比目魚肌細胞內鈣離子水平升高，細胞內鈣離子靜息濃度的增加一方面激活calpain ，增加收縮蛋白的降解，使肌肉萎縮；草四軍醫大月卜祠成士學位論文另一方面通過激活鈣調神經磷酸酶，增加快型mhc基因的表達，使骨骼肌肌球蛋白重鏈（ mhc ）發生由慢型向快型的轉化。
  4. Clinical investigation and nursing care of neuralgic amyotrophy

    神經痛性肌萎縮的臨床觀察與護理
  5. Effect of fk506 on neurological improvement in patients with amyotrophic lateral sclerosis following olfactory ensheathing cell transplantation

    506對嗅鞘細胞移植治療肌萎縮側索硬化癥患者神經功能改善的影響
  6. The department also develops and applies the up - to - date new treatment for the diseases which cannot be effectively treat before, such as motor neuron disease, intractable epilepsy, stroke, dementia, and muscular dystrophy

    在治療上引進最新的療法與歐美新開發藥物以治療在過去無法醫治的神經疾病，包括各種不隨意運動癥，癲癇癥、腦中風、失智癥及肌萎縮癥之治療。
  7. “ i have two sons. my older son is 22 and is in an advanced stage of muscular dystrophy. my younger son is 21 and has been diagnosed as chronically mentally ill

    我有2個兒子.我的大兒子22歲，已經是肌肉萎縮癥的晚期.我的小兒子21歲，被診斷為慢性精神疾病
  8. There is loss of anterior horn cells, so that patients present with progressive weakness that proceeds to paralysis from neurogenic muscular atrophy

    存在前角細胞喪失，因此病人表現為漸進性衰弱，這可能因神經源性肌萎縮而出現癱瘓。
  9. Alternatively, they could generate healthy specialized cells from patients who had donated their genetic material, and transplant them into tissues - - without the risk of prompting immune rejection - - to treat failing hearts, neurological diseases such as parkinson ' s disease and amyotrophic lateral sclerosis, spinal cord injury and diabetes

    上述二者中，他們可從被診為患遺傳疾病的病人中生成指定的健康細胞，並將其移植培養為組織不存在排斥免疫方面的風險可治療心臟衰竭，神經疾病如帕金森癥，肌萎縮性（脊髓）側索硬化癥，骨髓病癥和糖尿病。
  10. Biological and histological changes of denervated skeletal muscular atrophy

    失神經支配骨骼肌萎縮的生物學和組織學變化
  11. Effect of quot; fufang taizishen keli quot; on denervated muscle atrophy of rat

    復方太子參顆粒影響大鼠失神經支配骨骼肌萎縮的實驗研究
  12. Results the clinical features showed progressive muscle weakness in upper limb ; emg showed neurogenic changes, motor and sensory nerve conductive velocity was normal ; nerve repetetive stimulation showed decreased response ; muscle histochemistry revealed neurogenic findings ; ultra - eletronmicroscopy was not abnormal

    結果該例患者表現為進行性肌肉力弱，肌電圖顯示神經源性損害，神經重復刺激檢查示波幅下降，肌肉病理顯示小簇狀肌肉萎縮，電鏡下除極少數肌纖維膜溶解外其他未見特殊。
  13. The patient was a 71 year old man who developed muscle wasting and weakness and had electromyographic evidence of motor neuron disease

    患者是71歲男性，漸發肌肉萎縮和無力，肌電圖描記的證據顯示為運動神經元病。
  14. Als is a degeneratie disease of the nere cell of the spinal cord. they control oluntary muscle moements

    退變神經所支配的肌肉最終會由於能力喪失而萎縮。
  15. Since his early 20s, he has suffered from amyotrophic lateral sclerosis ( als ), a progressive deterioration of the central nervous system that usually causes death within three or four years

    因為在20年代早期他患上了肌萎縮性脊髓側索硬化癥（ als ） ，中樞神經系統逐漸變壞以至於通常會在三至四年內導致死亡。
  16. The muscular dystrophy association of canada provides relevant and current information about many types of neuromuscular disorders in an easy to understand format

    加拿大肌肉萎縮學會：以易解的方式提供數種神經肌肉失能類型的相關與即時資訊。
  17. Heriditary neuropathies come in many shapes and sizes. charcot - marie - tooth type 2 ( cmt2 ) causes degeneration of peripheral sensory and motor neurons, particularly at the ends of these long axons

    遺傳性神經病具有多種特點和方式。 2型腓骨肌萎縮癥（ cmt 2 ）導致外周特別是長軸突末端的感覺和運動神經元退化。
  18. In treating spinal cord injury, als or multiple sclerosis, the strategy may be to induce stem cells to yield a subset of glial cells called oligodendrocytes

    對脊髓損傷、側索硬化肌萎縮癥或多發性硬化癥而言，治療策略是要誘導幹細胞去製造神經膠質細胞中一群稱為寡突細胞的細胞。
  19. Magnetic resonance diffusion tensor imaging : quantitative measurements on upper motor neuron of patients with amyotrophic lateral sclerosis

    磁共振擴散張量成像對肌萎縮側索硬化癥患者上運動神經元病變的定量評估意義
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