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Citation(s)

  •   Gordon PH, Cheng B, Katz IB, Mitsumoto H, Rowland LP
    Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS. Neurology. 2009 Jun 2;72(22):1948-52. doi: 10.1212/WNL.0b013e3181a8269b.
  •   Strong MJ, Gordon PH
    Primary lateral sclerosis, hereditary spastic paraplegia and amyotrophic lateral sclerosis: discrete entities or spectrum? Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Mar;6(1):8-16. Review.
  •   Tartaglia MC, Rowe A, Findlater K, Orange JB, Grace G, Strong MJ
    Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up. Arch Neurol. 2007 Feb;64(2):232-6.

Oxidative Stress in Motor Neuron Disease: COSMOS-PLS Add-On Study

Details for clinical trial NCT01143428