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. 2015 Jan 12;112(4):E361–E370. doi: 10.1073/pnas.1414974112

Table 2.

Exp. 1: Biological motion perceptual thresholds of patients and controls

Patient Threshold Versus healthy age-matched controls (control group 1) Versus brain-damaged controls (control group 3)
All (n = 54) LH damage only (n = 43) RH damage only (n = 11) With “critical” pSTS lesion (n = 9) With “critical” vPMC lesion (n = 10)
Mean threshold ± SD t P t P t P t P t P t P
EL 18.38 19.15 ± 8.74 −0.086 0.933 1.47 0.15* 1.5 0.14* 1.29 0.22* 4.187 0.002* 3.66 0.003*
GB 18.73 19.15 ± 8.74 −0.047 0.963 1.54 0.13* 1.57 0.12* 1.35 0.20* 4.319 0.002* 3.78 0.003*
SH 11.33 19.15 ± 8.74 −0.866 0.401 0.12 0.90 0.09 0.93 0.22 0.83 1.528 0.082* 1.27 0.117*
CR 13.97 28.66 ± 7.91 −1.8 0.09 0.63 0.53 0.62 0.53 0.62 0.54 2.52 0.018* 2.17 0.03*
SM 12.25 25.06 ± 7.54 −1.64 0.12 0.3 0.77 0.27 0.78 0.36 0.72 1.875 0.049* 1.58 0.07*
EC 9.57 20.08 ± 7.87 −1.29 0.22 −0.21 0.83 −0.26 0.79 −0.047 0.96 0.864 0.206* 0.676 0.26*

Thresholds indicate the number of noise points masking the stimuli while performance is at 82% accuracy (Methods). Statistical values (t, P) represent single-case vs. control group comparisons (40). Ventral visual patients’ perceptual thresholds for biological motion were not significantly different from those of three control groups: healthy age-matched (group 1), brain-damaged (group 3), and younger controls (group 2; see Results). Importantly, the group of ventral patients performed significantly better than the group of patients with lesions to pSTS or vPMC (Results).

*

At the upper end of the controls’ distribution (i.e., performing better than the average).