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Signs of lasting benefit from amyloid Immunotherapy

ALS can be phenotypically classified into either limb onset (LO) cases with upper and lower motor neurons being affected, accounting for 70% of the cases, or Bulbar onset (25%) in which speech and swallowing issues first arise that are followed by later stage limb weakness (Zarei et al., 2015)

rodent data show lean-mass and bone-related endpoints with minimal prostate stimulation, while neuron studies report protection from excitotoxic challenge

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clinical trials, review articles or guidelines

doi: 10.1016/j.redox.2013.01.002