In recent years, there have been significant breakthroughs in the treatment of Amyotrophic Lateral Sclerosis (ALS), providing hope for patients and researchers alike. New approaches are emerging that offer promising avenues for managing this debilitating neurodegenerative disease. Researchers have identified potential drug candidates that target specific molecular pathways involved in Amyotrophic Lateral Sclerosis (ALS) treatment progression, aiming to slow down or halt the disease's effects. Additionally, advances in neuroprotective strategies and the use of stem cell therapies show promise in repairing and replacing damaged motor neurons.
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