“…DQEMG has been shown to be a valid and reliable tool for obtaining information regarding MU number, size, and complexity within healthy subjects, as well as from patients with neuromuscular disease and peripheral neuropathy (Boe et al, 2004;McNeil et al, 2005a,b;Boe et al, 2006Boe et al, , 2009Boe et al, , 2010Calder et al, 2008;Berger et al, 2011;Doherty, 2012, 2014;Allen et al, 2013). Using these techniques, we can evaluate the extent of collateral reinnervation following MU loss and the stability of neuromuscular transmission.…”