Dermic-derived fibroblasts for the study of amyotrophic lateral sclerosis
Javier Riancho1
Sara Arozamena2
Adolfo López de Munaín3
1.Service of Neurology,Hospital Sierrallana-IDIVAL,Torrelavega,Spain;Department of Medicine and Psychiatry,University of Cantabria,Santander,Spain;Centro de Investigación en Red de Enfermedades Neurodegenerativas,Instituto CarlosⅢ,Madrid,Spain2.Service of Neurology,Hospital Sierrallana-IDIVAL,Torrelavega,Spain3.Centro de Investigación en Red de Enfermedades Neurodegenerativas,Instituto CarlosⅢ,Madrid,Spain;Neurosciences Area,Biodonostia Research Institute;Service of Neurology,Hospital Universitario Donostia;Department of Neurosciences,School of Medicine and Nursery,University of the Basque Country,San Sebastián,Spain
摘要：Among neurodegenerative diseases,amyotrophic lateral scle-rosis (ALS) is the most frequent one involving motor neurons (MNs).ALS incidence varies throughout the world ranging from 0.7 to 4 cases per 100,000 habitants and year (Riancho et al.,2016).
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论文发表日期：2020-11-28
在线出版日期：2025-08-15（本平台首次上网日期，不代表文献的发表时间）
页数：2( 2043-2044 )