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- Amyotrophic lateral sclerosis (ALS) is uncommon. 肌萎縮側索硬化(ALS)很少見(jiàn)。
- They are absent in a patient with amyotrophic lateral sclerosis (ALS). 對于患肌萎縮側索硬化( ALS )病人來(lái)說(shuō)，不可能看到前角細胞。
- acute lateral sclerosis 急性側索硬化
- But, unfortunately, at age 21 he developed the first symptoms of amyotrophic lateral sclerosis (ALS). 但不幸的是，霍金在21歲那年首次顯現出側邊肌肉萎縮硬化癥狀，現在他幾乎全身癱瘓，不能言語(yǔ)。
- Amyotrophic lateral sclerosis(ALS) involves upper neuron,lower neuron and corticospinal tract. 肌萎縮側索硬化癥累及部位包括上、下運動(dòng)神經(jīng)元以及皮質(zhì)脊髓束。
- I am quite often asked: How do you feel about having ALS (amyotrophic lateral sclerosis)? 經(jīng)常會(huì )有人問(wèn)我：你患了肌萎縮性脊髓側索硬化癥，對此你怎么看？
- Amyotrophic lateral sclerosis(ALS)is a fatal neurodegenerative disorder characterized by progressive loss of motoneurons. 肌萎縮側索硬化(ALS)是一種運動(dòng)神經(jīng)元的進(jìn)行性變性疾病。
- Amyotrophic lateral sclerosis (ALS) is a chronic progressive neurodegenerative disease by the selective death of motor neurones. 肌萎縮側索硬化癥(amyotrophic lateral sclerosis,ALS)是一組選擇性侵犯運動(dòng)神經(jīng)元的慢性進(jìn)行性變性疾病。
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease, selectively involving in the upper and lower motor neurons. 肌萎縮側索硬化(Amyotrophic Lateral Sclerosis, ALS)是選擇性侵犯上、下運動(dòng)神經(jīng)元的慢性進(jìn)行性變性疾病。
- Amyotrophic lateral sclerosis (ALS)is a fatal neurodegenerative disorder characterized by progressive loss of motoneurons. 摘要肌萎縮側索硬化(ALS)是一種運動(dòng)神經(jīng)元的進(jìn)行性變性疾病。
- Patrick Aebischer and Ann C.Kato have been working together to study amyotrophic lateral sclerosis (ALS) using animal models since 1993. 艾畢雪和卡托自1993年起開(kāi)始合作，利用動(dòng)物模型研究肌萎縮性偏側硬化癥。
- Objective To figure out the relationship between Amyotrophic lateral sclerosis (ALS) and glutamate concenlra-tions of plasma and CSF. 目的了解肌萎縮側索硬化癥(ALS)患者血漿、腦脊液谷氨酸濃度的改變,為治療提供依據。
- Alzheimer s disease (AD), Parkinson s disease (PD), and amyotrophic lateral sclerosis (ALS) are the most common neurodegeneration disorders. 阿爾茨海默病、帕金森病、肌萎縮側索硬化癥等是最常見(jiàn)的神經(jīng)退行性疾病。
- Where are the anterior horn cells in this section of spinal cord? They are absent in a patient with amyotrophic lateral sclerosis (ALS). 脊髓切片上哪里是前角細胞?對于患肌萎縮側索硬化(ALS)病人來(lái)說(shuō)，不可能看到前角細胞。
- Background: Several groups have found that a significant percentage of patients with amyotrophic lateral sclerosis (ALS) have cognitive impairment. 背景：一些研究發(fā)現ALS患者存在認知障礙。
- Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by selective loss of motor neurons in the cortex, brainstem, and spinal cord. 肌萎縮側索硬化(amyotrophic lateral sclerosis, ALS)是一種以選擇性運動(dòng)皮質(zhì)、腦干及脊髓運動(dòng)神經(jīng)元丟失為特征的致死性神經(jīng)變性疾病。
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease, selectively involving the upper and lower motor neurons that control voluntary movement. 肌萎縮側索硬化（Amyotrophic Lateral Sclerosis，ALS）是一種支配隨意運動(dòng)的上下運動(dòng)神經(jīng)元選擇性受累的神經(jīng)系統變性疾病。
- Objective To study the clinical features of amyotrophic lateral sclerosis (ALS), and provide clinical data for the further research in pathogenesis and therapy. 目的探討肌萎縮側索硬化的臨床特點(diǎn),為進(jìn)一步的病因、治療研究提供臨床資料。
- Meanwhile, a man with amyotrophic lateral sclerosis - known as ALS or Lou Gerhig's Disease - has written a handbook on the condition, with the help of volunteers. 另外，一個(gè)患有漸凍人癥狀的患者在慈濟的幫忙下，完成他寫(xiě)漸凍人手冊的心愿；
- Methods: The following data were obtained through 112 amyotrophic lateral sclerosis (ALS). Three groups can be distinguished:(1) definite ALS (43) (2) possible ALS(38) (3) suspected ALS (31). 方法:將112例ALS患者分為確診43例,擬診38例,可疑31例,其中確診、擬診的患者代表典型ALS患者,可疑組均為單純下運動(dòng)神經(jīng)元綜合征的患者。
