
肌萎縮性脊髓側索硬化症
For around a decade, scientists have been trying to regrow nerve cells lost in neurodegenerative diseases such as Parkinson's, Alzheimer's and amyotrophic lateral sclerosis (ALS) from stem cells.
大約十年間,科學家們一直嘗試利用幹細胞使神經退變性疾病中的神經細胞再生,例如帕金森病,阿爾茨默病和肌萎縮側索硬化。
Objective: To evaluate combined tests of thoracic paraspinal muscles and sternocleidomastoid muscle and tongue muscles with electromyography as diagnostic aids in amyotrophic lateral sclerosis (ALS).
目的探讨胸段棘旁肌、胸鎖乳突肌、舌肌肌電圖聯合檢測在肌萎縮側索硬化(ALS)診斷中的價值。
But at age 21 he developed the first symptoms of amyotrophic lateral sclerosis (ALS), a disorder that would inevitably render him paralyzed and incapable of performing most kinds of work.
可是他在21歲的時候,出現了肌萎縮性(脊髓)側索硬化的征兆;這一疾病不可避免地要導緻癱瘓,使他很多事都不能做。
AIM: To analyze the correlation of the 4 clinical scale methods of amyotrophic lateral sclerosis and evaluate the concordance and synergistic effect in the application of clinic.
目的:分析肌萎縮側索硬化症臨床常用的4種評分方法之間的相關性,評價其臨床應用中的一緻性與協同效應。
Objective To observe the neural electrical pathological changes on amyotrophic lateral sclerosis(ALS)and to evaluate their clinical significance primarily.
目的觀察肌萎縮側索硬化(ALS)的電生理改變,并對其臨床意義作初步評價。
Hawking has ALS, or amyotrophic lateral sclerosis, which has confined him to a wheelchair and leaves him unable to speak without the help of a computerized voice synthesizer.
霍金患有肌萎縮性脊髓側索硬化症,簡稱ALS,他隻能坐在輪椅上,說話必須依賴電腦語音發生器。
Doctors gave him only a limited lifespan after he was diagnosed at the age age of 22 with the incurable disease of the muscles and nervous system, Amyotrophic Lateral Sclerosis.
在22歲的時候他被診斷患有肌肉和神經系統不可治愈的疾病——肌肉萎縮性脊髓側索硬化症,并且醫生說他的壽命不會很長。
They could also aid in the basic research of diseases such as epilepsy and the amyotrophic lateral sclerosis (ALS).
星形膠質細胞在癫痫和肌肉側索硬化症(ALS)的基礎研究中同樣有幫助。
Objective To investigate upper motor neurons involvement in amyotrophic lateral sclerosis (ALS) by diffusion tensor imaging (DTI) and magnetic resonance spectroscopy (MRS).
目的應用擴散張量成像(DTI)和磁共振波譜成像(MRS)研究肌萎縮側索硬化(ALS)上運動神經元受累情況。
Objective Investigate MR resonance diffusion tensor im-aging (DTI) characteristics of non-pyramid tracts in the patients with amyotrophic lateral sclerosis(ALS).
目的研究肌萎縮側索硬化症(ALS)患者非錐體束區域磁共振擴散張量成像(DTI)的特點。
Amyotrophic lateral sclerosis is a fatal neurodegenerative disease that is familial in 10% of cases.
肌萎縮性側束硬化症是一種緻命的神經退化性疾病,其家族遺傳率是10%。
For their attempt to develop embryonic stem-cell lines to model diseases such as amyotrophic lateral sclerosis .
他們努力發展胚胎幹細胞系以建立一些疾病的模型,如肌萎縮側索硬化症的模型。
Labs are using such cells to study amyotrophic lateral sclerosis, Parkinson's disease, Huntington's disease, and even autism.
實驗室通過這些細胞來研究肌萎縮性脊髓側索硬化、帕金森氏症、亨廷頓氏病,甚至自閉症。
Objective To investigate the features of F-wave and nerve conduction in patients with amyotrophic lateral sclerosis (ALS).
目的探讨肌萎縮側索硬化症(ALS)F波和神經傳導改變的特點。
It's a fundraising game called the Ice Bucket Challenge and it aims to raise awareness for amyotrophic lateral sclerosis (ALS).
這個名為“冰桶挑戰”的遊戲其實是一個的籌款項目,為對抗肌萎縮性脊髓側索硬化症(ALS)籌款,并引起更多人對該疾病的關注。
ObjectiveTo investigate the pathologic characteristics of the sural nerve in amyotrophic lateral sclerosis.
目的闡明肌萎縮側索硬化症患者腓腸神經的病理改變特點。
He was diagnosed with amyotrophic lateral sclerosis, the most common form of motor neurone disease, which confined him to a wheelchair and forced him to speak through an electronic voicebox.
他後來被确診為患有運動神經病中最常見的一種---肌萎縮性脊髓側索硬他症,這使得他隻得在輪椅上度過餘生,而且還得借助電子音箱說話。
Aim:To evaluate the characteristics of the decrement to repetitive nerve stimulation(RNS)in patients with amyotrophic lateral sclerosis(ALS).
目的:研究肌萎縮側索硬化(ALS)患者重複電刺激時複合肌肉動作電位波幅衰減的特點和影響因素。
I am quite often asked: How do you feel about having ALS (amyotrophic lateral sclerosis)?
經常會有人問我:你患了肌萎縮性脊髓側索硬化症,對此你怎麼看?
There is a disease called Amyotrophic Lateral Sclerosis (ALS).
世界上還有這樣的一種疾病——漸凍人症。
Amyotrophic lateral sclerosis (ALS) is uncommon.
肌萎縮側索硬化(ALS )很少見。
Objective: To observe the curative effect of TCM for amyotrophic lateral sclerosis(ALS) and expound the understanding of ALS in TCM.
前言:目的:觀察中醫藥治療肌萎縮側索硬化症的臨床療效,并試圖闡明中醫對本病的認識。
肌萎縮側索硬化症(Amyotrophic Lateral Sclerosis,ALS)是一種累及運動神經元的進行性神經系統疾病,屬于神經退行性疾病範疇。其名稱源自希臘語和拉丁語詞根:"amyotrophic"(肌肉萎縮,由"a-"無、"myo"肌肉、"trophic"營養構成)、"lateral"(脊髓側索區域)和"sclerosis"(組織硬化)。
從病理機制看,ALS主要表現為:
根據美國國家神經疾病和中風研究院(NINDS)的臨床觀察,90%病例為散發性,10%與遺傳基因突變相關,如SOD1、C9ORF72等基因異常已被證實與疾病發展相關。病程發展存在個體差異,中位生存期通常為确診後3-5年,但部分患者如物理學家霍金存活超過50年,提示疾病異質性特征。
目前治療手段主要基于兩個層面:
世界衛生組織将其列為五大疑難神經疾病之一,全球發病率約為1-2.6/10萬人。近年研究聚焦于反義寡核苷酸療法(如Tofersen)和幹細胞移植等前沿領域,美國FDA已加速相關療法的審批流程。
肌萎縮側索硬化(Amyotrophic Lateral Sclerosis,ALS),俗稱“漸凍症”,是一種慢性、進行性神經退行性疾病。以下是對該術語的詳細解釋:
術語構成與詞源
疾病特征
病因與流行病學
臨床意義
可通過等來源進一步了解詳細醫學機制及最新研究進展。
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