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. Author manuscript; available in PMC: 2009 Sep 15.
Published in final edited form as: Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Sep;5(3):141–149. doi: 10.1080/14660820410017109

Figure 3.

Figure 3

NAA concentrations in each of the 12 possible/suspected ALS patients tracked longitudinally. Each colored line represents an individual subject. During the first three months NAA either decreases or remains stable in all of these subjects. Subsequent to the 3-month time point, this tendency is no longer present.