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2015 Apr 21;5(2):545-89

Amyotrophic lateral sclerosis Glial contributions to ALS progression Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by the progressive loss of motor neurons (Charcot, 1874)

Bethesda, MD, US

Tumours with no other apparent cause can be related to FXR and MYO5B variants both in paediatric and non-paediatric populations [9]

There are some mechanisms involved in GSH diminution: increased oxidation by intracellular oxidizing agents, increased conjugation to molecules, and increased exit across the cell membrane [137]