Related Articles
Distal hereditary motor neuropathy type 7B with Dynactin 1 mutation
Lack of an association between SCFD1 rs10139154 polymorphism and amyotrophic lateral sclerosis
Serum ferritin is a candidate biomarker of disease aggravation in amyotrophic lateral sclerosis
Effect of the human SOD1‑G93A gene on the Nrf2/ARE signaling pathway in NSC‑34 cells
Implications of white matter damage in amyotrophic lateral sclerosis (Review)