TARDBP and amyotrophic lateral sclerosis: Our findings corroborate the findings of 2 of 3 previous postmortem examinations of patients with FOSMN in which TDP43 inclusions were identified in the brainstem.3,7,8 This report provides further evidence that FOSMN may be considered a forme fruste of bulbar-onset ALS, a notion further supported by the behavioral change and TDP43 inclusions in the frontal cortex.