“…Certain perimetric techniques are customised to bias the assessment of specific precortical visual pathways, such as the fast-flickering luminancepedestal targets of temporal modulation perimetry (TMP), or flicker perimetry, that preferentially test the magnocellular pathway (Vingrys et al, 1994), or the blue-on-yellow stimuli of shortwavelength automated perimetry (SWAP), which preferentially tests the koniocellular pathway (Sample and Weinreb, 1990). Both TMP Badcock, 2004a, 2004b;McKendrick et al, 2000;Nguyen et al, 2014) and SWAP (McKendrick et al, 2002;Nguyen et al, 2014;Yenice et al, 2006;Yucel et al, 2005) have identified visual field defects in up to 50% of migraine cohorts. Note that these findings should not be interpreted as evidence for migraine producing a selective loss of one type of processing pathway, as dysfunction in both the magnocellular and parvocellular pathways has been demonstrated in people with migraine using perceptual stimuli designed to assess these channels separately (McKendrick and Badcock, 2003;McKendrick and Sampson, 2009).…”