“…In a clinical context, Yee et al (1985, p. 938) noted that due to the "maximal recruitment of motoneurons and extraocular muscle fibers […] during large saccades […] it would be expected that most disorders that impair the recruitment of motoneurons and muscle fibers or that otherwise interfere with the contraction of muscle fibers will decrease the peak velocity." Indeed, several pathologies are associated with alterations in saccadic peak velocity (Anderson & MacAskill, 2013), including progressive supranuclear palsy (Newman, Gay, Stroud, & Brooks 1970), Huntington's disease (Starr, 1967), and spinocerebellar degeneration (Zee, Optican, Cook, Robinson, & Engel, 1976). Therefore, it is crucial that amplitude and peak velocity of saccades can be accurately measured and restored from the recorded data.…”