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Amyotrophic lateral sclerosis disease modifying therapeutics:a cell biological perspective

Amyotrophic lateral sclerosis disease modifying therapeutics:a cell biological perspective
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摘要 Amyotrophic lateral sclerosis(ALS)is a progressively fatal neuromuscular disorder classically characterized by loss of upper and lower motor neurons from the cortex to the spinal cord Diagnosed patients have a median survival of about 3 years and death usually results from eventual respiratory failure. Amyotrophic lateral sclerosis(ALS)is a progressively fatal neuromuscular disorder classically characterized by loss of upper and lower motor neurons from the cortex to the spinal cord Diagnosed patients have a median survival of about 3 years and death usually results from eventual respiratory failure.
作者 Bor Luen Tang
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第3期407-408,共2页 中国神经再生研究(英文版)
基金 supported by the NUS Graduate School for Integrative Sciences and Engineering
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