Amyotrophic Lateral Sclerosis (ALS) patients usually exhibit symptoms of brain damage related to their disease sub-type. Researchers have evidence that patients with bulbar-onset ALS have more extensive
Continue readingStudies have shown that patients of Amyotrophic Lateral Sclerosis (ALS) with cognitive difficulties exhibit brain damage in the brain regions that are necessary for thinking. This aspect has been attributed
Continue readingAmyotrophic Lateral Sclerosis (ALS) can be regarded as one of the most fatal neurodegenerative diseases and is characterised by affecting the upper and lower motor neurons. Notably, all motor functions
Continue readingRecent scientific observations have shown that Amyotrophic Lateral Sclerosis (ALS) patients who have progressed to an advanced stage of the disease experience difficulties in controlling their muscles.
Continue readingCompletely paralysed Amyotrophic Lateral Sclerosis (ALS) patients who were also unable to talk can now communicate. They make use of a computer interface that can detect their thoughts by monitoring their
Continue readingA recent report from researchers following a study demonstrated that patients with Amyotrophic Lateral Sclerosis (ALS) who develop Frontotemporal Syndrome (FTS), have their lives cut short in spite of
Continue readingNot so long ago, researchers reviewed the strengths and weaknesses of animal models currently in use for Amyotrophic Lateral Sclerosis (ALS) research. The study looked into the transition from animal models
Continue readingAmyotrophic Lateral Sclerosis (ALS) continues to affect and consume the lives of thousands of people around the world. A new and different therapy that suppresses specific gene expressions is currently
Continue readingThe ALS Association defines ALS, Amyotrophic Lateral Sclerosis, as “a neurodegenerative disease that affects nerve cells in the brain and the spinal cord”. It is a condition where the muscles of the
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