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Primary lateral sclerosis as a phenotypic manifestation of familial ALS 家族性ALS表型表现为原发性侧索硬化症
primary lateral sclerosis 原生性脊髓侧索硬化
Amyotrophic lateral sclerosis (ALS) is uncommon. 肌萎缩侧索硬化(ALS)很少见。
They are absent in a patient with amyotrophic lateral sclerosis (ALS). 对于患肌萎缩侧索硬化( ALS )病人来说，不可能看到前角细胞。
primary lateral spinal sclerosis 原发性脊髓侧索硬化
She had known for three months before my wedding that she had a terminal disease, amyotrophic lateral sclerosis (Lou Gehrig's disease). 她在我们婚礼前3个月就得知她患有末期肌肉萎缩硬化症。
But, unfortunately, at age 21 he developed the first symptoms of amyotrophic lateral sclerosis (ALS). 但不幸的是，霍金在21岁那年首次显现出侧边肌肉萎缩硬化症状，现在他几乎全身瘫痪，不能言语。
Amyotrophic lateral sclerosis(ALS) involves upper neuron,lower neuron and corticospinal tract. 肌萎缩侧索硬化症累及部位包括上、下运动神经元以及皮质脊髓束。
I am quite often asked: How do you feel about having ALS (amyotrophic lateral sclerosis)? 经常会有人问我：你患了肌萎缩性脊髓侧索硬化症，对此你怎么看？
She had known for three months before my wedding that she had a terminal disease,amyotrophic lateral sclerosis (Lou Gehrig's disease). 她在我们婚礼前3个月就得知，她患有末期肌肉萎缩硬化症。
The analysis of SOD-1 activity in red blood cells about Familial amyotrophic lateral sclerosis of the Han and Zhuang nationatity in China. 中国壮、汉族家族性肌萎缩侧索硬化症之红细胞内SOD-1活性分析。
Amyotrophic lateral sclerosis(ALS)is a fatal neurodegenerative disorder characterized by progressive loss of motoneurons. 肌萎缩侧索硬化(ALS)是一种运动神经元的进行性变性疾病。
Amyotrophic lateral sclerosis (ALS) is a chronic progressive neurodegenerative disease by the selective death of motor neurones. 肌萎缩侧索硬化症(amyotrophic lateral sclerosis,ALS)是一组选择性侵犯运动神经元的慢性进行性变性疾病。
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease, selectively involving in the upper and lower motor neurons. 肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis, ALS)是选择性侵犯上、下运动神经元的慢性进行性变性疾病。
Amyotrophic lateral sclerosis (ALS)is a fatal neurodegenerative disorder characterized by progressive loss of motoneurons. 摘要肌萎缩侧索硬化(ALS)是一种运动神经元的进行性变性疾病。
Patrick Aebischer and Ann C.Kato have been working together to study amyotrophic lateral sclerosis (ALS) using animal models since 1993. 艾毕雪和卡托自1993年起开始合作，利用动物模型研究肌萎缩性偏侧硬化症。
Objective To figure out the relationship between Amyotrophic lateral sclerosis (ALS) and glutamate concenlra-tions of plasma and CSF. 目的了解肌萎缩侧索硬化症(ALS)患者血浆、脑脊液谷氨酸浓度的改变,为治疗提供依据。
The center is taking aim at neurological diseases, including Alzheimer's, Parkinson's, amyotrophic lateral sclerosis, and diabetic neuropathy. 中心集中力量进行神经系统疾病的药物开发，包括阿尔茨海默氏症、帕金森氏症、肌萎缩侧索硬化、糖尿病性神经病等。
Alzheimer s disease (AD), Parkinson s disease (PD), and amyotrophic lateral sclerosis (ALS) are the most common neurodegeneration disorders. 阿尔茨海默病、帕金森病、肌萎缩侧索硬化症等是最常见的神经退行性疾病。
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细胞?对于患肌萎缩侧索硬化(ALS)病人来说，不可能看到前角细胞。