https://www.pisavisionlab.org/2026/09/10/primary-visual-cortex-bold-responses-to-relative-localization-of-sounds-at-7t/https://www.pisavisionlab.org/2026/09/10/harnessing-brain-plasticity-to-improve-binocular-vision-in-amblyopia-an-evidence-based-update/https://www.pisavisionlab.org/2026/09/10/impairment-in-understanding-grasping-movements-in-egocentric-and-allocentric-perspectives-in-children-with-cerebral-palsy-due-to-periventricular-leukomalacia/https://www.pisavisionlab.org/2026/09/10/development-of-higher-level-vision-a-network-perspective/https://www.pisavisionlab.org/2026/09/10/the-duration-effect-of-short-term-monocular-deprivation-measured-by-binocular-rivalry-and-binocular-combination/https://www.pisavisionlab.org/2026/09/10/development-of-bold-response-to-motion-in-human-infants/https://www.pisavisionlab.org/2026/09/10/quantum-spin-models-for-numerosity-perception/https://www.pisavisionlab.org/2026/09/09/numerosity-adaptation-across-size-transformations/https://www.pisavisionlab.org/2026/07/23/altered-cortical-synchronization-in-photosensitive-idiopathic-generalized-epilepsy/https://www.pisavisionlab.org/2026/07/23/speed-of-visual-processing-across-the-visual-field/https://www.pisavisionlab.org/2026/07/23/late-cortical-dynamics-mediate-numerosity-illusions-induced-by-symmetry/https://www.pisavisionlab.org/2026/07/23/meyelens-an-affordabel-open-source-3d-printable-eyewear-platform-for-pupillometry-and-gaze-tracking/https://www.pisavisionlab.org/2026/07/09/visually-guided-voluntary-actions-boost-short-term-ocular-dominance-plasticity/https://www.pisavisionlab.org/2026/07/09/short-term-monocular-deprivation-in-healthy-humans-a-meta-analysis-and-new-perspectives/https://www.pisavisionlab.org/2026/07/08/no-aftereffect-of-motor-duration-production-on-auditory-duration-perception/https://www.pisavisionlab.org/2026/07/08/receptive-fields-from-single-neuron-recording-and-mri-reveal-similar-information-coding-for-binocular-depth/https://www.pisavisionlab.org/2026/07/08/characterizing-human-disparity-tuning-properties-using-population-receptive-field-mapping/https://www.pisavisionlab.org/2026/06/12/groupitizing-a-visuo-spatial-and-arithmetic-phenomenon/https://www.pisavisionlab.org/2026/06/12/color-selective-numerosity-adaptation-depends-on-the-automatic-categorization-of-colored-information/https://www.pisavisionlab.org/2026/06/12/stronger-reliance-on-visual-perceptual-history-in-individuals-with-higher-math-anxiety/https://www.pisavisionlab.org/2026/06/12/the-role-of-physical-and-cognitive-effort-on-time-perception/https://www.pisavisionlab.org/2026/06/12/virtual-reality-as-an-innovative-tool-for-numerosity-perception/https://www.pisavisionlab.org/2026/06/12/sensorimotor-numerosity-uniquely-supports-arithmetic-development-in-children/https://www.pisavisionlab.org/2026/05/26/saccade-synchronized-alpha-rhythms-predict-strength-of-memory-trace-of-stimulus-orientation/https://www.pisavisionlab.org/2026/05/15/is-number-a-primary-perceptual-attribute/https://www.pisavisionlab.org/2026/05/13/local-and-global-influence-of-contextual-information-insight-from-auditory-and-visual-speed-perception/https://www.pisavisionlab.org/2026/05/13/human-visionmaintains-a-richrepresentation-ofobjects-movingbehind-an-occluder/https://www.pisavisionlab.org/2026/05/13/adaptation-acts-directly-on-the-sensory-representation-of-numerosity/https://www.pisavisionlab.org/2025/12/16/the-pulvinar-regulates-plasticity-in-human-visual-cortex/https://www.pisavisionlab.org/2025/11/27/art-induced-psychological-well-being-individual-traits-shape-the-beneficial-effects-of-aesthetic-experiences/https://www.pisavisionlab.org/2025/11/27/dimensionality-reduction-techniques-in-pupillometry-research-a-primer-for-behavioral-scientists/https://www.pisavisionlab.org/2025/11/27/visual-search-performance-depends-on-the-congruency-of-olfactory-sensations/https://www.pisavisionlab.org/2025/11/18/monocular-delay-during-visually-guided-actions-is-as-effective-as-monocular-deprivation-in-driving-ocular-dominance-plasticity/https://www.pisavisionlab.org/2025/11/05/short-term-monocular-deprivation-changes-thalamo-cortical-connectivity-measured-with-ultra-high-field-fmriduring-visual-stimulation/https://www.pisavisionlab.org/2025/11/05/short-term-monocular-deprivation-in-adult-humans-ameta-analysis-and-new-perspectives/https://www.pisavisionlab.org/2025/11/05/acute-supplementation-of-beta-hydroxybutyrateincreasesvisual-cortical-excitability-in-humans-a-combinedelectro-encephalographyand-magnetic-resonancespectroscopy-study/https://www.pisavisionlab.org/2025/09/01/color-crowding-considered-as-adaptive-spatial-integration/https://www.pisavisionlab.org/2025/08/22/continuous-tracking-of-audiovisual-motion-2/https://www.pisavisionlab.org/2025/08/01/pupillometric-signature-of-implicit-learning-of-statistical-regularities/https://www.pisavisionlab.org/2025/07/29/the-speed-of-visual-discrimination-differs-between-foveola-and-perifovea-a-combined-eeg-and-behavioral-investigation/https://www.pisavisionlab.org/2025/07/29/multisensory-number-channels-derived-from-individual-differences/https://www.pisavisionlab.org/2025/07/29/continuous-tracking-of-audiovisual-motion/https://www.pisavisionlab.org/2025/07/09/optimal-feature-encoding-in-early-vision/https://www.pisavisionlab.org/2025/04/22/pupil-size-as-a-biomarker-of-cognitive-dysfunctions-toward-a-physiologically-informed-screening-of-mental-states/https://www.pisavisionlab.org/2025/03/26/the-visual-system-does-not-operate-like-a-camera/https://www.pisavisionlab.org/2025/03/26/recent-but-not-long-term-priors-induce-behavioral-oscillations-in-peri-saccadic-vision/https://www.pisavisionlab.org/2025/02/18/reply-to-failure-to-replicate-a-superiority-effect-in-crowding/https://www.pisavisionlab.org/2024/10/23/positive-serial-dependence-in-ratings-of-food-images-for-appeal-and-calories/https://www.pisavisionlab.org/2024/10/04/pupillometric-signature-of-implicit-learning-2/https://www.pisavisionlab.org/2024/10/04/active-vision-shapes-ocular-dominance-4/https://www.pisavisionlab.org/2024/10/04/weakened-sustained-attention-and-increased-cognitive-effort-after-total-sleep-deprivation-a-virtual-reality-ecological-study/https://www.pisavisionlab.org/2024/09/10/plasticity-of-the-adult-human-brain-fmri-and-pupillometry/https://www.pisavisionlab.org/2024/09/09/active-vision-shapes-ocular-dominance-3/https://www.pisavisionlab.org/2024/09/09/monocular-delay-during-active-vision-shifts-ocular-dominance-2/https://www.pisavisionlab.org/2024/09/09/monocular-delay-during-active-vision-shifts-ocular-dominance/https://www.pisavisionlab.org/2024/09/09/ocular-dominance-plasticity-in-the-adult-brain-beyond-short-term-changes-insights-from-7t-bold-responses-in-amblyopic-patients/https://www.pisavisionlab.org/2024/09/09/treating-adult-amblyopia-through-combined-physical-exercise-and-inverse-occlusion-evidence-from-7t-bold-responses/https://www.pisavisionlab.org/2024/09/09/correlated-p300b-and-phasic-pupil-dilation-responses-to-motivationally-significant-stimuli/https://www.pisavisionlab.org/2024/09/07/number-adaptation-reply/https://www.pisavisionlab.org/2024/09/07/what-pupil-size-can-and-cannot-tell-about-math-anxiety/https://www.pisavisionlab.org/2024/09/07/reshaping-the-peripersonal-space-in-virtual-reality-2/https://www.pisavisionlab.org/2024/09/07/electrophysiological-correlates-of-temporal-numerosity-adaptation/https://www.pisavisionlab.org/2024/09/07/serial-dependence-in-perception/https://www.pisavisionlab.org/2024/09/07/auditory-time-perception-impairment-in-children-with-developmental-dyscalculia/https://www.pisavisionlab.org/2024/09/07/neurocognitive-assessment-of-mathematics-related-capacities-in-neurosurgical-patients/https://www.pisavisionlab.org/2024/09/07/the-role-of-motor-effort-on-the-sensorimotor-number-system/https://www.pisavisionlab.org/2024/09/06/pupillometry-indexes-ocular-dominance-plasticity/https://www.pisavisionlab.org/2024/09/03/neural-substrates-for-early-data-reduction-in-fast-vision-a-psychophysical-investigation/https://www.pisavisionlab.org/2024/07/08/effectiveness-of-labels-in-digital-art-experience-psychophysiological-and-behavioral-evidence/https://www.pisavisionlab.org/2024/04/08/adaptation-to-numerosity-affects-the-pupillary-light-response/https://www.pisavisionlab.org/2024/04/08/disambiguating-vision-with-sound/https://www.pisavisionlab.org/2024/04/08/investigating-cross-orientation-inhibition-with-continuous-tracking/https://www.pisavisionlab.org/2023/12/21/remapping-of-peripersonal-space-in-virtual-reality-an-exploratory-study/https://www.pisavisionlab.org/2023/12/21/neurophysiological-investigation-of-numerosityadaptation/https://www.pisavisionlab.org/2023/12/21/task-dependent-interaction-between-stimulus-numerosity-and-duration/https://www.pisavisionlab.org/2023/12/21/drivers-performance-assessment-approaching-pedestrian-crossings-through-the-analysis-of-the-speed-and-perceptive-data-recorded-during-on-field-tests/https://www.pisavisionlab.org/2023/12/07/the-italian-colour-lexicon-in-tuscany-elicited-lists-cognitive-salience-and-semantic-maps-of-colour-terms/https://www.pisavisionlab.org/2023/12/07/saccadic-trajectories-deviate-toward-or-away-from-optimally-informative-visual-features/https://www.pisavisionlab.org/2023/12/07/psychophysiological-and-behavioral-responses-to-descriptive-labels-in-modern-art-museums/https://www.pisavisionlab.org/2023/12/07/time-estimation-during-motor-activity/https://www.pisavisionlab.org/2023/12/07/fast-discrimination-of-fragmentary-images-the-role-of-local-optimal-information/https://www.pisavisionlab.org/2023/11/19/math-difficulties-in-attention-deficit-hyperactivity-disorder-do-not-originate-from-the-visual-number-sense/https://www.pisavisionlab.org/2023/11/19/eeg-signature-of-grouping-strategies-in-numerosity-perception/https://www.pisavisionlab.org/2023/11/19/the-symmetry-induced-numerosity-illusion-depends-on-visual-attention/https://www.pisavisionlab.org/2023/11/19/sensorimotor-mechanisms-selective-to-numerosity-evidence-from-individual-differences/https://www.pisavisionlab.org/2023/11/19/reshaping-the-peripersonal-space-in-virtual-reality/https://www.pisavisionlab.org/2023/11/19/similar-effect-of-running-on-visual-and-auditory-time-perception-in-the-ranges-of-milliseconds-and-seconds/https://www.pisavisionlab.org/2023/11/19/action-shaped-perception-towards-a-reunification-of-two-systems/https://www.pisavisionlab.org/2023/11/19/visual-p2p-component-responds-to-perceived-numerosity/https://www.pisavisionlab.org/2023/11/15/serial-dependence-in-face-gender-classification-revealed-in-low-beta-frequency-eeg/https://www.pisavisionlab.org/2023/11/10/prolonged-and-short-epileptiform-discharges-have-an-opposite-relationship-with-the-sleep-wake-cycle-in-patients-with-jme-implications-for-eeg-recording-protocols/https://www.pisavisionlab.org/2023/11/10/expanding-the-spectrum-of-oculocutaneous-albinism-does-isolated-foveal-hypoplasia-really-exist/https://www.pisavisionlab.org/2023/11/10/all-eyes-on-attention/https://www.pisavisionlab.org/2023/11/10/the-readiness-potential-correlates-with-action-linked-modulation-of-visual-accuracy/https://www.pisavisionlab.org/2023/11/10/active-vision-how-you-look-reflects-what-you-are-looking-for/https://www.pisavisionlab.org/2023/11/10/visual-priming-and-serial-dependence-are-mediated-by-separate-mechanisms/https://www.pisavisionlab.org/2023/11/10/symmetry-as-a-grouping-cue-for-numerosity-perception/https://www.pisavisionlab.org/2023/11/10/crowding-results-from-optimal-integration-of-visual-targets-with-contextual-information/https://www.pisavisionlab.org/2023/11/10/vision-neuronal-mechanisms-enabling-stable-perception/https://www.pisavisionlab.org/2023/11/10/the-role-of-non-numerical-information-in-the-perception-of-temporal-numerosity/https://www.pisavisionlab.org/2023/11/10/serial-dependence-improves-performance-and-biases-confidence-based-decisions/https://www.pisavisionlab.org/2023/11/10/serial-dependence-in-orientation-judgments-at-the-time-of-saccades/https://www.pisavisionlab.org/2023/11/10/autistic-individuals-show-less-grouping-induced-bias-in-numerosity-judgments/https://www.pisavisionlab.org/2023/10/31/active-vision-gates-ocular-dominance-plasticity-in-human-adults/https://www.pisavisionlab.org/2023/10/16/pupillometric-signature-of-implicit-learning/https://www.pisavisionlab.org/2023/10/16/short-term-monocular-deprivation-in-adult-humans-alterspulvino-cortical-functional-connectivity-measured-withresting-state-fmri-at-ultra-high-field-2/https://www.pisavisionlab.org/2023/10/16/preferential-pupillary-responses-to-very-fast-motion/https://www.pisavisionlab.org/2023/10/16/short-term-monocular-deprivation-in-adult-humans-alterspulvino-cortical-functional-connectivity-measured-withresting-state-fmri-at-ultra-high-field/https://www.pisavisionlab.org/2023/10/16/active-vision-shapes-ocular-dominance-2/https://www.pisavisionlab.org/2023/10/09/active-vision-shapes-ocular-dominance/https://www.pisavisionlab.org/2023/10/09/attention-cueing-in-rivalry-insights-from-pupillometry-2/https://www.pisavisionlab.org/2023/10/09/synchronization-between-music-dynamics-and-heart-rhythm-is-modulated-by-the-musicians-emotional-involvement-a-single-case-study/https://www.pisavisionlab.org/2023/09/25/the-role-of-neural-oscillations-in-visuo-motor-communication-at-the-time-of-saccades/https://www.pisavisionlab.org/2023/09/25/serial-dependence-inperception/https://www.pisavisionlab.org/2023/09/15/measuring-the-reliability-of-binocular-rivalry/https://www.pisavisionlab.org/2023/08/25/short-term-monocular-deprivation-in-adult-humans-alters-pulvino-cortical-functional-connectivity-measured-withresting-state-fmri-at-ultra-high-field/https://www.pisavisionlab.org/2023/08/25/development-of-local-global-preference-in-vision-and-haptics/https://www.pisavisionlab.org/2023/08/21/evidence-of-serial-dependence-from-decoding-of-visual-evoked-potentials/https://www.pisavisionlab.org/2023/08/21/long-covid-where-we-stand-and-challenges-ahead/https://www.pisavisionlab.org/2023/08/21/mutual-interaction-between-visual-homeostatic-plasticity-and-sleep-in-adult-humans/https://www.pisavisionlab.org/2023/08/21/covid-19-vaccines-where-we-stand-and-challenges-ahead/https://www.pisavisionlab.org/2023/07/24/effect-of-fasting-on-short-term-visual-plasticity-in-adult-humans/https://www.pisavisionlab.org/2022/12/12/how-to-choose-a-research-paper-writing-service-3/https://www.pisavisionlab.org/2022/12/12/how-to-choose-a-research-paper-writing-service-2/https://www.pisavisionlab.org/2022/12/12/how-to-choose-a-research-paper-writing-service/https://www.pisavisionlab.org/2022/12/12/free-essay-checkers/https://www.pisavisionlab.org/2022/12/09/10-best-essay-writing-services-top-paper-writing-websites/https://www.pisavisionlab.org/2022/12/09/greatest-essay-writing-companies-prime-10-writing-websites-reviewed-in-2022/https://www.pisavisionlab.org/2022/12/07/tips-for-ordering-essays-online/https://www.pisavisionlab.org/2022/11/25/the-visual-system/https://www.pisavisionlab.org/2022/11/25/short-term-monocular-deprivation-in-adult-humans-alters-functional-brain-connectivity-measured-with-ultra-high-field-magnetic-resonance-imaging-2/https://www.pisavisionlab.org/2022/09/27/pupil-size-automatically-encodes-numerosity/https://www.pisavisionlab.org/2022/09/27/skipping-breakfast-changes-visual-processing-incretins-contribution-to-short-term-visual-plasticity%ef%bf%bc/https://www.pisavisionlab.org/2022/09/27/analogous-development-of-local-global-preference-in-vision-and-touch-%ef%bf%bc/https://www.pisavisionlab.org/2022/09/27/impact-of-ketonic-metabolism-on-cortical-visual-processing/https://www.pisavisionlab.org/2022/09/25/investigating-the-trajectory-of-the-development-of-local-global-preference-in-vision-and-haptics%ef%bf%bc/https://www.pisavisionlab.org/2022/09/25/pupillometric-index-of-locus-coeruleus-degeneration-in-alzheimer-disease/https://www.pisavisionlab.org/2022/09/25/pupil-size-as-an-index-of-ocular-dominance-plasticity-2/https://www.pisavisionlab.org/2022/09/25/short-term-monocular-deprivation-in-adult-humans-alters-functional-brain-connectivity-measured-with-ultra-high-field-magnetic-resonance-imaging/https://www.pisavisionlab.org/2022/07/20/bariatric-surgery-restores-visual-cortical-plasticity-in-nondiabetic-subjects-with-obesity-2/https://www.pisavisionlab.org/2022/07/06/the-multimodal-number-sense-spanning-space-time-sensory-modality-and-action-2/https://www.pisavisionlab.org/2022/07/05/vision-optimizing-each-glimpse/https://www.pisavisionlab.org/2022/07/05/attention-cueing-in-rivalry-insights-from-pupillometry/https://www.pisavisionlab.org/2022/06/24/numerosity-perception-is-tuned-to-salient-environmental-features-2/https://www.pisavisionlab.org/2022/06/24/does-more-imply-better-vision%ef%bf%bc/https://www.pisavisionlab.org/2022/06/21/mathematics-and-numerosity-but-not-visuo-spatial-working-memory-correlate-with-math-anxiety-in-young-adults/https://www.pisavisionlab.org/2022/06/20/auditory-time-thresholds-in-the-range-of-milliseconds-but-not-seconds-are-impaired-in-adhd-3/https://www.pisavisionlab.org/2022/06/20/the-grouping-induced-numerosity-illusion-is-attention-dependent-2/https://www.pisavisionlab.org/2022/06/15/influence-of-motor-and-cognitive-tasks-on-time-estimation/https://www.pisavisionlab.org/2022/06/15/information-optimal-local-features-automatically-attract-covert-and-overt-attention/https://www.pisavisionlab.org/2022/05/26/the-dynamics-of-grouping-induced-biases-in-apparent-numerosity-revealed-by-a-continuous-tracking-technique%ef%bf%bc/https://www.pisavisionlab.org/2022/05/26/reduced-2d-form-coherence-and-3d-structure-from-motion-sensitivity-in-developmental-dyscalculia%ef%bf%bc/https://www.pisavisionlab.org/2022/05/25/contextual-information-modulates-pupil-size-in-autistic-children/https://www.pisavisionlab.org/2022/05/25/short-term-plasticity-in-the-human-visual-thalamus/https://www.pisavisionlab.org/2022/04/11/unimpaired-groupitizing-in-children-and-adolescents-with-dyscalculia/https://www.pisavisionlab.org/2022/04/11/pupil-size-as-an-index-of-ocular-dominance-plasticity/https://www.pisavisionlab.org/2022/03/25/mathematics-and-numerosity-but-not-visuo-spatial-working-memory-correlate-with-mathematical-anxiety-in-adults/https://www.pisavisionlab.org/2022/02/07/auditory-time-thresholds-in-the-range-of-milliseconds-but-not-seconds-are-impaired-in-adhd-2/https://www.pisavisionlab.org/2022/02/07/ideal-observer-analysis-for-continuous-tracking-experiments/https://www.pisavisionlab.org/2022/01/31/a-predictive-pedestrian-crash-model-based-on-artificial-intelligence-techniques/https://www.pisavisionlab.org/2022/01/31/normal-retinotopy-in-primary-visual-cortex-in-a-congenital-complete-unilateral-lesion-of-lateral-geniculate-nucleus-in-human-a-case-study/https://www.pisavisionlab.org/2022/01/31/uncertainty-and-prior-assumptions-rather-than-innate-logarithmic-encoding-explain-nonlinear-number-to-space-mapping/https://www.pisavisionlab.org/2022/01/31/numbers-in-action/https://www.pisavisionlab.org/2022/01/31/visual-duration-but-not-numerosity-is-distorted-while-running/https://www.pisavisionlab.org/2021/12/11/groupitizing-modifies-neural-coding-of-numerosity/https://www.pisavisionlab.org/2021/11/24/propagation-and-update-of-auditory-perceptual-priors-through-alpha-and-theta-rhythms/https://www.pisavisionlab.org/2021/11/24/differential-diagnosis-in-children-with-autistic-symptoms-and-subthreshold-ados-total-score-an-observational-study/https://www.pisavisionlab.org/2021/11/24/perceptual-history-acts-in-world-centred-coordinates/https://www.pisavisionlab.org/2021/11/24/sex-differences-in-autism-spectrum-disorder-an-investigation-on-core-symptoms-and-psychiatric-comorbidity-in-preschoolers/https://www.pisavisionlab.org/2021/11/24/objective-pupillometry-shows-that-perceptual-styles-covary-with-autistic-like-personality-traits-2/https://www.pisavisionlab.org/2021/11/24/clinical-characterization-of-a-6-year-old-patient-with-autism-and-two-adjacent-duplications-on-10q11-22q11-23-a-case-report/https://www.pisavisionlab.org/2021/11/24/implicit-visuospatial-attention-shapes-numerosity-adaptation-and-perception/https://www.pisavisionlab.org/2021/11/24/evidence-for-an-a-modal-number-sense-numerosity-adaptation-generalizes-across-visual/https://www.pisavisionlab.org/2021/11/24/white-matter-deficits-correlate-with-visual-motion-perception-impairments-in-dyslexic-carriers-of-the-dcdc2-genetic-risk-variant/https://www.pisavisionlab.org/2021/11/24/the-grouping-induced-numerosity-illusion-is-attention-dependent/https://www.pisavisionlab.org/2021/11/24/the-pupil-responds-spontaneously-to-perceived-numerosity/https://www.pisavisionlab.org/2021/11/24/subitizing-unlike-estimation-does-not-process-sets-in-parallel/https://www.pisavisionlab.org/2021/10/18/meye-web-app-for-translational-and-real-time-pupillometry/https://www.pisavisionlab.org/2021/10/14/pupil-responses-to-implied-motion-in-figurative-and-abstract-paintings/https://www.pisavisionlab.org/2021/10/14/pupillary-response-to-real-illusory-and-implied-motion/https://www.pisavisionlab.org/2021/10/14/early-visual-saliency-based-on-isolated-optimal-features/https://www.pisavisionlab.org/2021/07/13/perception-of-geometric-sequences-and-numerosity-both-predict-formal-geometric-competence-in-primary-school-children/https://www.pisavisionlab.org/2021/06/21/groupitizing-improves-estimation-of-numerosity-of-auditory-sequences/https://www.pisavisionlab.org/2021/06/16/predictive-visuo-motor-communication-through-neural-oscillations/https://www.pisavisionlab.org/2021/05/24/tapping-force-encodes-metrical-aspects-of-rhythm-2/https://www.pisavisionlab.org/2021/05/24/cortical-thickness-of-primary-visual-cortex-correlates-with-motion-deficits-in-periventricular-leukomalacia-2/https://www.pisavisionlab.org/2021/05/22/typical-crossmodal-numerosity-perception-in-preterm-newborns/https://www.pisavisionlab.org/2021/04/29/grouping-induced-numerosity-biases-vary-with-autistic-like-personality-traits/https://www.pisavisionlab.org/2021/04/22/tapping-force-encodes-metrical-aspects-of-rhythm/https://www.pisavisionlab.org/2021/03/26/an-audio-visual-multisensory-training-enhances-the-visual-processing-of-motion-stimuli-in-healthy-participants-an-electrophysiological-study/https://www.pisavisionlab.org/2021/03/26/early-v5-processing-decoupled-from-awareness-with-fast-but-not-slow-moving-stimuli-tms-evidence-for-dynamic-deployment-of-parallel-pathways-depending-on-motion-velocity/https://www.pisavisionlab.org/2021/03/26/visual-field-defects-and-cortical-plasticity-after-an-audio-visual-multisensory-stimulation/https://www.pisavisionlab.org/2021/03/26/the-role-of-v1-independent-networks-in-visual-field-defects-recovery/https://www.pisavisionlab.org/2021/03/26/transcranial-direct-current-stimulation-and-visuo-spatial-contextual-learning-reveal-homeostatic-regulatory-principles-in-the-human-posterior-parietal-cortex-2/https://www.pisavisionlab.org/2021/03/26/transcranial-direct-current-stimulation-and-visuo-spatial-learning-the-interaction-between-stimulation-dependent-and-brain-activity-dependent-mechanisms/https://www.pisavisionlab.org/2021/03/26/transcranial-direct-current-stimulation-and-visuo-spatial-contextual-learning-reveal-homeostatic-regulatory-principles-in-the-human-posterior-parietal-cortex/https://www.pisavisionlab.org/2021/03/26/electrophysiological-correlates-of-the-effects-induced-by-an-audio-visual-training-on-healthy-participants/https://www.pisavisionlab.org/2021/03/26/multisensory-stimulation-boosts-orienting-responses-and-attenuates-intact-field-attention-processing-in-hemianopia/https://www.pisavisionlab.org/2021/03/26/numerosity-adaptation-partly-depends-on-the-allocation-of-implicit-numerosity-contingent-visuo-spatial-attention/https://www.pisavisionlab.org/2021/03/26/tdcs-over-posterior-parietal-cortex-increases-cortical-excitability-but-decreases-learning-an-erps-and-tms-eeg-study/https://www.pisavisionlab.org/2021/03/25/the-link-between-math-anxiety-and-numerosity-perception/https://www.pisavisionlab.org/2021/03/25/spatial-but-not-temporal-numerosity-thresholds-correlate-with-formal-math-skills-in/https://www.pisavisionlab.org/2021/03/25/time-and-numerosity-estimation-in-peripersonal-and-extrapersonal-space/https://www.pisavisionlab.org/2021/01/15/voluntary-action-rhythmically-modulates-7t-bold-visual-responses-in-primary-visual-cortex-2/https://www.pisavisionlab.org/2021/01/12/perceptual-history-propagates-down-to-early-levels-of-sensory-analysis-2/https://www.pisavisionlab.org/2021/01/12/perceptual-history-propagates-down-to-early-levels-of-sensory-analysis/https://www.pisavisionlab.org/2020/12/16/not-only-faces-specialized-visual-representation-of-human-hands-revealed-by-adaptation/https://www.pisavisionlab.org/2020/12/01/la-ricerca-in-tre-minuti-bright-night-2020/https://www.pisavisionlab.org/2020/11/26/tactile-numerosity-is-coded-in-external-space/https://www.pisavisionlab.org/2020/11/26/pupillary-response-to-representations-of-light-in-paintings/https://www.pisavisionlab.org/2020/11/23/a-sensorimotor-numerosity-system/https://www.pisavisionlab.org/2020/11/17/pupillary-responses-obey-emmerts-law-and-co-vary-with-autistic-traits/https://www.pisavisionlab.org/2020/11/16/location-and-object-based-attention-enhance-number-estimation/https://www.pisavisionlab.org/2020/11/12/pupillometry-in-mind-wandering-and-non-trial-based-experiments/https://www.pisavisionlab.org/2020/10/13/attentional-amplification-of-neural-codes-for-number-independent-of-other-quantities-along-the-dorsal-visual-stream/https://www.pisavisionlab.org/2020/10/09/the-rhythms-of-sensorimotor-integration-action-planning-and-perceptual-oscillations/https://www.pisavisionlab.org/2020/10/09/shaping-the-understanding-of-the-world-through-action-action-planning-and-behavioral-oscillations/https://www.pisavisionlab.org/2020/10/09/rhythms-in-perception-action-planning-and-behavioral-oscillations/https://www.pisavisionlab.org/2020/10/09/saccadic-suppression-is-embedded-within-extended-oscillatory-modulation-of-sensitivity/https://www.pisavisionlab.org/2020/10/09/voluntary-action-modulates-visually-evoked-cortical-responses-in-primary-visual-cortex-an-integrated-ultra-high-field-fmri-and-eeg-study-3/https://www.pisavisionlab.org/2020/10/09/spontaneous-pupillary-oscillations-increase-during-mindfulness-meditation-2/https://www.pisavisionlab.org/2020/10/09/the-shared-numerical-representation-for-action-and-perception-develops-independently-from-vision-2/https://www.pisavisionlab.org/2020/10/09/temporal-context-affects-interval-timing-at-the-perceptual-level/https://www.pisavisionlab.org/2020/10/09/the-role-of-temporal-and-spatial-attention-in-size-adaptation/https://www.pisavisionlab.org/2020/10/09/perceptual-oscillations-in-gender-classification-of-faces-contingent-on-stimulus-history/https://www.pisavisionlab.org/2020/10/09/object-identity-determines-trans-saccadic-integration/https://www.pisavisionlab.org/2020/10/09/learning-disabilities-developmental-dyscalculia/https://www.pisavisionlab.org/2020/10/09/grouping-strategies-in-number-estimation-extend-the-subitizing-range/https://www.pisavisionlab.org/2020/10/09/adaptation-to-the-speed-of-biological-motion-in-autism-2/https://www.pisavisionlab.org/2020/10/09/non-spatial-skills-differ-in-the-front-and-rear-peri-personal-space/https://www.pisavisionlab.org/2020/10/09/spontaneous-pupillary-oscillations-increase-during-mindfulness-meditation/https://www.pisavisionlab.org/2020/09/24/fast-saccadic-eye-movements-in-humans-suggest-that-numerosity-perception-is-automatic-and-direct-2/https://www.pisavisionlab.org/2020/09/24/fast-saccadic-eye-movements-in-humans-suggest-that-numerosity-perception-is-automatic-and-direct/https://www.pisavisionlab.org/2020/08/25/the-visual-white-matter-connecting-human-area-prostriata-and-the-thalamus-is-retinotopically-organized/https://www.pisavisionlab.org/2020/08/24/adaptation-to-hand-tapping-affects-sensory-processing-of-numerosity-directly-evidence-from-reaction-times-and-confidence-2/https://www.pisavisionlab.org/2020/08/24/horace-barlow-1921-2020/https://www.pisavisionlab.org/2020/08/24/groupitizing-a-strategy-for-numerosity-estimation/https://www.pisavisionlab.org/2020/07/21/recalibrating-time-perception-to-self-motion/https://www.pisavisionlab.org/2020/07/21/serial-dependence-in-perception-requires-conscious-awareness/https://www.pisavisionlab.org/2020/07/20/attraction-to-the-recent-past-in-aesthetic-judgments-a-positive-serial-dependence-for-rating-artwork/https://www.pisavisionlab.org/2020/07/20/auditory-perceptual-history-is-propagated-through-alpha-oscillations/https://www.pisavisionlab.org/2020/07/20/using-psychophysical-performance-to-predict-short-term-ocular-dominance-plasticity-in-human-adults/https://www.pisavisionlab.org/2020/07/17/a-closer-look-at-the-timecourse-of-mind-wandering-pupillary-responses-and-behaviour-2/https://www.pisavisionlab.org/2020/07/15/altered-visual-plasticity-in-morbidly-obese-subjects/https://www.pisavisionlab.org/2020/07/15/a-closer-look-at-the-timecourse-of-mind-wandering-pupillary-responses-and-behaviour/https://www.pisavisionlab.org/2020/07/13/oscillations-of-sensitivity-and-response-bias-in-auditory-perception/https://www.pisavisionlab.org/2020/07/13/adaptation-to-hand-tapping-affects-directly-sensory-processing-of-numerosity/https://www.pisavisionlab.org/2020/07/13/three-systems-for-visual-numerosity-a-single-case-study/https://www.pisavisionlab.org/2020/07/13/numerosity-adaptation-changes-in-sensory-processes-or-in-decision-making-2/https://www.pisavisionlab.org/2020/07/13/motor-adaptation-distorts-space/https://www.pisavisionlab.org/2020/07/13/specialized-visual-module-for-numerosity/https://www.pisavisionlab.org/2020/07/13/residual-visual-responses-in-patients-with-retinitis-pigmentosa-revealed-by-functional-magnetic/https://www.pisavisionlab.org/2020/07/13/the-number-sense-and-its-link-with-child-math-abilities-2/https://www.pisavisionlab.org/2020/07/13/psychophysical-evidence-for-a-generalized-number-sense-and-its-link-with-development-of-mathematical-abilities/https://www.pisavisionlab.org/2020/07/13/spontaneous-perception-of-numerosity-in-pre-schoolers/https://www.pisavisionlab.org/2020/07/13/numerosity-adaptation-changes-in-sensory-processes-or-in-decision-making/https://www.pisavisionlab.org/2020/07/13/neural-plasticity-of-the-visual-brain-in-infants-and-in-adults/https://www.pisavisionlab.org/2020/07/13/the-number-sense-and-its-link-with-child-math-abilities/https://www.pisavisionlab.org/2020/07/13/pupillometry-reveals-perceptual-differences-that-are-tightly-linked-to-autistic-traits/https://www.pisavisionlab.org/2020/07/13/pupillometry-reveals-perceptual-differences-linked-with-autistic-like-traits/https://www.pisavisionlab.org/2020/07/13/the-common-rhythm-of-action-and-perception/https://www.pisavisionlab.org/2020/07/12/inter-individual-differences-in-visual-perception-and-pupillometry-tools-to-study-them/https://www.pisavisionlab.org/2020/07/12/transaccadic-integration-perisaccadic-compression-building-visual-space-with-and-without-landmarks/https://www.pisavisionlab.org/2020/07/12/pupillometry-provides-new-insights-on-figure-ground-segregation-and-its-covariation-with-autistic-traits-2/https://www.pisavisionlab.org/2020/07/12/voluntary-action-modulates-visually-evoked-cortical-responses-in-primary-visual-cortex-an-integrated-ultra-high-field-fmri-and-eeg-study-2/https://www.pisavisionlab.org/2020/07/12/voluntary-action-modulates-visually-evoked-cortical-responses-in-primary-visual-cortex-an-integrated-ultra-high-field-fmri-and-eeg-study/https://www.pisavisionlab.org/2020/07/12/pupillometry-provides-new-insights-on-figure-ground-segregation-and-its-covariation-with-autistic-traits/https://www.pisavisionlab.org/2020/06/30/the-common-rhythm-of-action-and-perception-journal-of-cognitive-neuroscience-2/https://www.pisavisionlab.org/2020/06/29/voluntary-action-rhythmically-modulates-7t-bold-visual-responses-in-primary-visual-cortex/https://www.pisavisionlab.org/2020/06/29/vision-science-society-annual-meeting-on-line-event/https://www.pisavisionlab.org/2020/06/29/perceptual-expectancy-is-revealed-by-pupillo-me-try-and-correlates-with-autistic-traits/https://www.pisavisionlab.org/2020/06/29/perceptual-dynamics-predict-plasticity/https://www.pisavisionlab.org/2020/06/02/audio%e2%80%90visual-multisensory-training-enhances-visual-processing-of-motion-stimuli-in-healthy-participants-an-electrophysiological-study-european-journal-of-neuroscience-4410-2748-2758/https://www.pisavisionlab.org/2020/06/02/compensatory-recovery-after-multisensory-stimulation-in-hemianopic-patients-behavioral-and-neurophysiological-components-frontiers-in-systems-neuroscience-10-45/https://www.pisavisionlab.org/2020/06/02/the-role-of-the-retino-colliculo-extrastriate-pathway-in-visual-awareness-and-visual-field-recovery-neuropsychologia-90-72-79/https://www.pisavisionlab.org/2020/06/01/decoupling-of-early-v5-motion-processing-from-visual-awareness-a-matter-of-velocity-as-revealed-by-transcranial-magnetic-stimulation-journal-of-cognitive-neuroscience-3010-1517-1531/https://www.pisavisionlab.org/2020/06/01/posterior-brain-lesions-selectively-alter-alpha-oscillatory-activity-and-predict-visual-performance-in-hemianopic-patients-cortex-121-347-361/https://www.pisavisionlab.org/2020/06/01/alpha-oscillations-reveal-implicit-visual-processing-of-motion-in-hemianopia-cortex-122-81-96/https://www.pisavisionlab.org/2020/06/01/effects-of-different-transcranial-direct-current-stimulation-protocols-on-visuo-spatial-contextual-learning-formation-evidence-of-homeostatic-regulatory-mechanisms-scientific-reports-101/https://www.pisavisionlab.org/2020/06/01/shaping-the-visual-system-cortical-and-subcortical-plasticity-in-the-intact-and-the-lesioned-brain-neuropsychologia/https://www.pisavisionlab.org/2020/06/01/adult-cortical-plasticity-peaks-after-every-meal-ecvp-41nd-european-conference-on-visual-perception-ecvp-2018-trieste-italia/https://www.pisavisionlab.org/2020/06/01/behavioral-indices-of-plasticity-and-inhibition-change-with-metabolism-sensory-plasticity-adaptation-and-development-spade-workshop-2018-pisa-italia/https://www.pisavisionlab.org/2020/06/01/perceptual-dynamics-predict-plasticity-nextgenvis-workshop-pisa-italia-february-24-28-2019/https://www.pisavisionlab.org/2020/06/01/inter-individual-variability-of-short-term-ocular-dominance-plasticity-in-human-adultsecvp-42nd-edition-of-the-european-conference-on-visual-perception-leuven-belgium-august-25-29-2019/https://www.pisavisionlab.org/2020/06/01/inter-individual-variability-of-short-term-ocular-dominance-plasticity-in-human-adults-cnr-retreat-pisa-italia-october-2-4-2019/https://www.pisavisionlab.org/2020/06/01/inter-individual-variability-of-short-term-ocular-dominance-plasticity-in-human-adults2-nd-brayn-brainstorming-research-assembly-for-young-neuroscientists-milano-italia-november-14-16-2019/https://www.pisavisionlab.org/2020/06/01/indexing-arousal-with-pupillometry-and-eeg-implication-for-normal-vs-pathological-aging-2nd-brayn-brainstorming-research-assembly-for-young-neuroscientists-milano-italia-november-14-16-2019/https://www.pisavisionlab.org/2020/06/01/indexing-arousal-with-pupillometry-and-eeg-implication-for-normal-vs-pathological-aging-in-cnr-annual-retreat-2019-pisa-italia-october-2-4-2019/https://www.pisavisionlab.org/2020/06/01/inter-individual-variability-of-short-term-ocular-dominance-plasticity-in-human-adults-cvrs-17th-biennial-meeting-of-the-child-vision-research-society-pisa-italia-june-15-17-2019/https://www.pisavisionlab.org/2020/06/01/pupillometry-reveals-perceptual-differences-that-are-tightly-linked-to-autistic-traits-in-typical-adults-a-no-report-paradigm-based-on-stereopsis-cvrs-17th-biennial-meeting-of-the/https://www.pisavisionlab.org/2020/06/01/pupillometry-reveals-perceptual-differences-that-are-tightly-linked-to-autistic-traits-in-typical-adults-a-report-free-paradigm-based-on-stereopsis-2-nd-brayn-brainstorming-rese/https://www.pisavisionlab.org/2020/06/01/pupillometry-reveals-perceptual-differences-that-are-tightly-linked-to-autistic-traits-in-typical-adults-a-report-free-paradigm-based-on-stereopsis/https://www.pisavisionlab.org/2020/05/31/41st-european-conference-on-visual-perception-ecvp-2018-trieste/https://www.pisavisionlab.org/2020/05/31/a-how-attention-to-faces-and-objects-changes-over-time-in-toddlers-with-autism-spectrum-disorders-preliminary-evidence-from-an-eye-tracking-study-brain-sci-2019-9-344/https://www.pisavisionlab.org/2020/05/31/parental-perspectives-on-psychiatric-comorbidity-in-preschoolers-with-autism-spectrum-disorders-receiving-publicly-funded-mental-health-services-front-psychiatry-10107/https://www.pisavisionlab.org/2020/05/31/processing-of-natural-scenery-is-associated-with-lower-attentional-and-cognitive-load-compared-with-urban-ones-journal-of-environmental-psychology-62-1-11-2/https://www.pisavisionlab.org/2020/05/31/math-anxiety-mediates-the-link-between-number-sense-and-math-achievements-in-high-math-anxiety-young-adults/https://www.pisavisionlab.org/2020/05/31/motor-adaptation-distorts-visual-space/https://www.pisavisionlab.org/2020/05/30/asymmetrical-interference-between-number-and-item-size-perception-provides-evidence-for-a-domain-specific-impairment-in-dyscalculia/https://www.pisavisionlab.org/2020/05/30/mapping-numerical-perception-and-operations-in-relation-to-functional-and-anatomical-landmarks-of-human-parietal-cortex/https://www.pisavisionlab.org/2020/08/01/excessive-visual-crowding-effects-in-developmental-dyscalculia/https://www.pisavisionlab.org/2020/05/30/neuroplasticity-in-adult-human-visual-cortex-neuroscience-biobehavioral-reviews-volume-112-may-2020-pages-542-552/https://www.pisavisionlab.org/2020/05/24/prova-2020/https://www.pisavisionlab.org/2020/01/04/visual-clutter-causes-high-magnitude-errorsplos-biol-3-4-e56/https://www.pisavisionlab.org/2020/01/04/time-perception-space-time-in-the-braincurr-biol-5-16-r171-173/https://www.pisavisionlab.org/2020/01/04/the-effects-of-opposite-polarity-dipoles-on-the-detection-of-glass-patternsvision-res-6-7-46-1139-1144/https://www.pisavisionlab.org/2020/01/04/separate-attentional-resources-for-vision-and-auditionproc-biol-sci-1592-273-1339-1345/https://www.pisavisionlab.org/2020/01/04/resolution-for-spatial-segregation-and-spatial-localization-by-motion-signalsvision-res-6-7-46-932-939/https://www.pisavisionlab.org/2020/01/04/perceptual-synchrony-of-audiovisual-streams-for-natural-and-artificial-motion-sequencesj-vis-3-6-260-268/https://www.pisavisionlab.org/2020/01/04/perception-transient-disruptions-to-neural-space-timecurr-biol-19-16-r847-849/https://www.pisavisionlab.org/2020/01/04/development-of-saccadic-suppression-in-childrenj-neurophysiol-3-96-1011-1017/https://www.pisavisionlab.org/2020/01/04/contour-interactions-between-pairs-of-gabors-engaged-in-binocular-rivalry-reveal-a-map-of-the-association-fieldvision-res-8-9-46-1473-1487/https://www.pisavisionlab.org/2020/01/04/combining-visual-and-auditory-informationprog-brain-res-155-243-258/https://www.pisavisionlab.org/2020/01/04/auditory-attention-at-the-onset-of-west-syndrome-correlation-with-eeg-patterns-and-visual-functionbrain-dev-5-28-293-299/https://www.pisavisionlab.org/2020/01/04/on-the-possibility-of-a-unifying-framework-for-serial-dependencies-i-perception-66-1-16-3/https://www.pisavisionlab.org/2020/01/04/a-feature-tracking-model-simulates-the-motion-direction-bias-induced-by-phase-congruencyj-vis-3-6-179-195/https://www.pisavisionlab.org/2020/01/04/the-role-of-perceptual-learning-on-modality-specific-visual-attentional-effectsvision-res-1-47-60-70/https://www.pisavisionlab.org/2020/01/04/the-lowest-spatial-frequency-channel-determines-brightness-perceptionvision-res-10-47-1282-1291/https://www.pisavisionlab.org/2020/01/04/the-effect-of-optokinetic-nystagmus-on-the-perceived-position-of-briefly-flashed-targetsvision-res-6-47-861-868/https://www.pisavisionlab.org/2020/01/04/the-contribution-of-prefrontal-cortex-to-global-perceptionexp-brain-res-3-181-427-434/https://www.pisavisionlab.org/2020/01/04/spatiotopic-selectivity-of-bold-responses-to-visual-motion-in-human-area-mtnat-neurosci-2-10-249-255/https://www.pisavisionlab.org/2020/01/04/neural-mechanisms-for-timing-visual-events-are-spatially-selective-in-real-world-coordinatesnat-neurosci-4-10-423-425/https://www.pisavisionlab.org/2020/01/04/motor-coordination-in-children-with-congenital-strabismus-effects-of-late-surgeryeur-j-paediatr-neurol-5-11-285-291/https://www.pisavisionlab.org/2020/01/04/influence-of-saccadic-adaptation-on-spatial-localization-comparison-of-verbal-and-pointing-reportsj-vis-5-7-16-11-13/https://www.pisavisionlab.org/2020/01/04/abnormal-adaptive-face-coding-mechanisms-in-children-with-autism-spectrum-disordercurr-biol-17-17-1508-1512/https://www.pisavisionlab.org/2020/01/03/young-children-do-not-integrate-visual-and-haptic-form-informationcurr-biol-9-18-694-698/https://www.pisavisionlab.org/2020/01/03/the-knowing-visual-selftrends-cogn-sci-10-12-363-364/https://www.pisavisionlab.org/2020/01/03/the-assessment-of-visual-acuity-in-children-with-periventricular-damage-a-comparison-of-behavioural-and-electrophysiological-techniquesvision-res-10-48-1233-1241/https://www.pisavisionlab.org/2020/01/03/non-linear-integration-of-crowded-orientation-signalsvision-res-22-48-2352-2358/https://www.pisavisionlab.org/2020/01/03/neurodevelopmental-evolution-of-west-syndrome-a-2-year-prospective-studyeur-j-paediatr-neurol-5-12-387-397/https://www.pisavisionlab.org/2020/01/03/inversion-of-perceived-direction-of-motion-caused-by-spatial-undersampling-in-two-children-with-periventricular-leukomalaciaj-cogn-neurosci-6-20-1094-1106/https://www.pisavisionlab.org/2020/01/03/bold-response-to-spatial-phase-congruency-in-human-brainj-vis-10-8-15-11-15/https://www.pisavisionlab.org/2020/01/03/anti-glass-patterns-and-real-motion-perception-same-or-different-mechanismsj-vis-2-8-1-1-15/https://www.pisavisionlab.org/2020/01/03/a-visual-sense-of-numbercurr-biol-6-18-425-428/https://www.pisavisionlab.org/2020/01/03/search-superiority-in-autism-within-but-not-outside-the-crowding-regimevision-res-16-49-2151-2156/https://www.pisavisionlab.org/2020/01/03/pooling-and-segmenting-motion-signalsvision-res-10-49-1065-1072/https://www.pisavisionlab.org/2020/01/03/neural-correlates-of-texture-and-contour-integration-in-children-with-autism-spectrum-disordersvision-res-16-49-2140-2150/https://www.pisavisionlab.org/2020/01/03/motion-perception-in-preterm-children-role-of-prematurity-and-brain-damageneuroreport-15-20-1339-1343/https://www.pisavisionlab.org/2020/01/03/mislocalization-of-flashed-and-stationary-visual-stimuli-after-adaptation-of-reactive-and-scanning-saccadesj-neurosci-35-29-11055-11064/https://www.pisavisionlab.org/2020/01/03/meaningful-auditory-information-enhances-perception-of-visual-biological-motionj-vis-4-9-25-21-27/https://www.pisavisionlab.org/2020/01/03/cueing-the-interpretation-of-a-necker-cube-a-way-to-inspect-fundamental-cognitive-processescogn-process-10-suppl-1-s95-99/https://www.pisavisionlab.org/2020/01/03/auditory-dominance-over-vision-in-the-perception-of-interval-durationexp-brain-res-1-198-49-57/https://www.pisavisionlab.org/2020/01/03/visual-information-gleaned-by-observing-grasping-movement-in-allocentric-and-egocentric-perspectivesproc-biol-sci-1715-278-2142-2149/https://www.pisavisionlab.org/2020/01/03/vision-keeping-the-world-still-when-the-eyes-movecurr-biol-10-20-r442-444/https://www.pisavisionlab.org/2020/01/03/vision-senses-number-directlyj-vis-2-10-10-11-18/https://www.pisavisionlab.org/2020/01/03/the-contribution-of-scene-context-on-change-detection-performancevision-res-20-50-2062-2068/https://www.pisavisionlab.org/2020/01/03/subitizing-but-not-estimation-of-numerosity-requires-attentional-resourcesj-vis-6-10-20/https://www.pisavisionlab.org/2020/01/03/study-protocol-safety-and-efficacy-of-propranolol-in-newborns-with-retinopathy-of-prematurity-prop-rop-isrctn18523491bmc-pediatr-10-83/https://www.pisavisionlab.org/2020/01/03/reported-quality-of-randomized-controlled-trials-in-neglect-rehabilitationneurol-sci-2-31-159-163/https://www.pisavisionlab.org/2020/01/03/poor-haptic-orientation-discrimination-in-nonsighted-children-may-reflect-disruption-of-cross-sensory-calibrationcurr-biol-3-20-223-225/https://www.pisavisionlab.org/2020/01/03/plasticity-of-the-visual-system-after-early-brain-damagedev-med-child-neurol-10-52-891-900/https://www.pisavisionlab.org/2020/01/03/motor-signals-in-visual-localizationj-vis-6-10-2/https://www.pisavisionlab.org/2020/01/03/cortical-visual-function-in-preterm-infants-in-the-first-yearj-pediatr-4-156-550-555/https://www.pisavisionlab.org/2020/01/03/contrast-reduction-and-reading-assessment-and-reliability-with-the-reading-explorer-testeur-j-ophthalmol-2-20-389-396/https://www.pisavisionlab.org/2020/01/03/compression-of-time-during-smooth-pursuit-eye-movementsvision-res-24-50-2702-2713/https://www.pisavisionlab.org/2020/01/03/brain-development-critical-periods-for-cross-sensory-plasticitycurr-biol-21-20-r934-936/https://www.pisavisionlab.org/2020/01/03/alpha-waves-a-neural-signature-of-visual-suppressionexp-brain-res-3-4-207-213-219/https://www.pisavisionlab.org/2020/01/03/adaptation-and-mislocalization-fields-for-saccadic-outward-adaptation-in-humansjournal-of-eye-movement-research-4-3-1-18/https://www.pisavisionlab.org/2020/01/02/reduced-perceptual-sensitivity-for-biological-motion-in-paraplegia-patientscurr-biol-22-21-r910-911/https://www.pisavisionlab.org/2020/01/02/spatiotopic-visual-maps-revealed-by-saccadic-adaptation-in-humans-curr-biol-2011-aug-2321161380-4/https://www.pisavisionlab.org/2020/01/02/perceived-duration-of-visual-and-tactile-stimuli-depends-on-perceived-speed-front-integr-neurosci-551/https://www.pisavisionlab.org/2020/01/02/visual-perception-more-than-meets-the-eyecurr-biol-4-21-r159-161/https://www.pisavisionlab.org/2020/01/02/the-role-of-holistic-processing-in-face-perception-evidence-from-the-face-inversion-effectvision-res-11-51-1273-1278/https://www.pisavisionlab.org/2020/01/02/vision-and-audition-do-not-share-attentional-resources-in-sustained-tasksfront-psychol-2-56/https://www.pisavisionlab.org/2020/01/02/spatiotopic-coding-of-bold-signal-in-human-visual-cortex-depends-on-spatial-attentionplos-one-7-6-e21661/https://www.pisavisionlab.org/2020/01/02/spatiotopic-coding-and-remapping-in-humansphilos-trans-r-soc-lond-b-biol-sci-1564-366-504-515/https://www.pisavisionlab.org/2020/01/02/reward-sharpens-orientation-coding-independently-of-attentionfront-neurosci-5-13/https://www.pisavisionlab.org/2020/01/02/motion-psychophysics-1985-2010vision-res/https://www.pisavisionlab.org/2020/01/02/greater-sparing-of-visual-search-abilities-in-children-after-congenital-rather-than-acquired-focal-brain-damageneurorehabil-neural-repair/https://www.pisavisionlab.org/2020/01/02/eye-position-effects-in-oculomotor-plasticity-and-visual-localizationj-neurosci-20-31-7341-7348/https://www.pisavisionlab.org/2020/01/02/cross-sensory-facilitation-reveals-neural-interactions-between-visual-and-tactile-motion-in-humansfront-psychol-2-55/https://www.pisavisionlab.org/2020/01/02/applying-the-helmholtz-illusion-to-fashion-horizontal-stripes-wont-make-you-look-fatteriperception-1-2-69-76/https://www.pisavisionlab.org/2020/01/02/adaptation-affects-both-high-and-low-subitized-numbers-under-conditions-of-high-attentional-loadseeing-and-perceiving-24-141-150/https://www.pisavisionlab.org/2020/01/02/acoustic-cues-to-visual-detection-a-classification-image-studyj-vis-6-11/https://www.pisavisionlab.org/2020/01/02/constructing-stable-spatial-maps-of-the-worldperception-11-41-1355-1372/https://www.pisavisionlab.org/2020/01/02/plasticita-ed-adattabilita-della-visionegiornale-italiano-di-psicologia-3-517-522/https://www.pisavisionlab.org/2020/01/02/the-development-of-speed-discrimination-abilitiesvision-res-70-27-33/https://www.pisavisionlab.org/2020/01/02/active-movement-restores-veridical-event-timing-after-tactile-adaptationj-neurophysiol-8-108-2092-2100/https://www.pisavisionlab.org/2020/01/02/when-the-world-becomes-too-real-a-bayesian-explanation-of-autistic-perceptiontrends-cogn-sci-10-16-504-510/https://www.pisavisionlab.org/2020/01/02/impaired-visual-size-discrimination-in-children-with-movement-disordersneuropsychologia-8-50-1838-1843/https://www.pisavisionlab.org/2020/01/02/spatiotopic-perceptual-maps-in-humans-evidence-from-motion-adaptationproc-biol-sci-1740-279-3091-3097/https://www.pisavisionlab.org/2020/01/02/a-comparative-study-of-face-processing-using-scrambled-facesperception-4-41-460-473/https://www.pisavisionlab.org/2020/01/02/visual-motion-distorts-visual-and-motor-space-j-vis-2-12/https://www.pisavisionlab.org/2020/01/02/spatiotemporal-dynamics-of-perisaccadic-remapping-in-humans-revealed-by-classification-imagesj-vis-4-12-11/https://www.pisavisionlab.org/2019/12/30/selective-tuning-for-contrast-in-macaque-area-v4j-neurosci-47-33-18583-18596/https://www.pisavisionlab.org/2019/12/30/spatial-position-information-accumulates-steadily-over-time-j-neurosci-334718396-18401/https://www.pisavisionlab.org/2019/12/30/optimal-multimodal-integration-in-spatial-localizationj-neurosci-333514259-14268/https://www.pisavisionlab.org/2019/12/30/blood-oxygen-level-dependent-activation-of-the-primary-visual-cortex-predicts-size-adaptation-illusionj-neurosci-40-33-15999-16008/https://www.pisavisionlab.org/2019/12/30/visual-sustained-attention-and-numerosity-sensitivity-correlate-with-math-achievement-in-childrenj-exp-child-psychol-2-116-380-391/https://www.pisavisionlab.org/2019/12/30/the-vertical-horizontal-illusion-assessing-the-contributions-of-anisotropy-abutting-and-crossing-to-the-misperception-of-simple-line-stimulij-vis-8-13/https://www.pisavisionlab.org/2019/12/30/erratum-to-contextual-effects-in-interval-duration-judgements-in-vision-audition-and-touchexp-brain-res/https://www.pisavisionlab.org/2019/12/30/contextual-effects-in-interval-duration-judgements-in-vision-audition-and-touchexp-brain-res/https://www.pisavisionlab.org/2019/12/30/bold-human-responses-to-chromatic-spatial-featureseur-j-neurosci-2-38-2290-2299/https://www.pisavisionlab.org/2019/12/30/perceptual-motor-abilities-in-pre-school-preterm-childrenearly-hum-dev/https://www.pisavisionlab.org/2019/12/30/a-mechanism-for-detecting-coincidence-of-auditory-and-visual-spatial-signalsmultisens-res-4-26-333-345/https://www.pisavisionlab.org/2019/12/30/the-motion-silencing-illusion-results-from-global-motion-and-crowdingj-vis-5-13/https://www.pisavisionlab.org/2019/12/30/the-new-visual-neuroscience-mit-press/https://www.pisavisionlab.org/2019/12/30/compromised-approximate-number-system-acuity-in-school-aged-children-born-extremely-pretermdev-med-child-neurol/https://www.pisavisionlab.org/2019/12/30/spatiotopic-neural-representations-develop-slowly-across-saccadescurr-biol-5-23-r193-194/https://www.pisavisionlab.org/2019/12/30/spatio-temporal-topography-of-saccadic-overestimation-of-timevision-res-83c-56-65/https://www.pisavisionlab.org/2019/12/30/congenital-nystagmus-in-two-infants-born-from-mothers-exposed-to-methadone-during-pregnancyital-j-pediatr-1-39-40/https://www.pisavisionlab.org/2019/12/30/long-integration-time-for-accelerating-and-decelerating-visual-tactile-and-visuo-tactile-stimuli-multisensory-research-1-2-26-53-68/https://www.pisavisionlab.org/2019/12/30/children-do-not-recalibrate-motor-sensory-temporal-order-after-exposure-to-delayed-sensory-feedbackdev-sci/https://www.pisavisionlab.org/2019/12/30/a-generalized-sense-of-number-proc-r-soc-b-2014/https://www.pisavisionlab.org/2019/12/30/the-visual-component-to-saccadic-compressionj-vis-12-14/https://www.pisavisionlab.org/2019/12/30/musical-training-generalises-across-modalities-and-reveals-efficient-and-adaptive-mechanisms-for-reproducing-temporal-intervalsacta-psychol-amst-147-25-33/https://www.pisavisionlab.org/2019/12/30/impairment-of-auditory-spatial-localization-in-congenitally-blind-human-subjectsbrain-pt-1-137-288-293/https://www.pisavisionlab.org/2019/12/30/buildup-of-spatial-information-over-time-and-across-eye-movementsbehavioural-brain-research/https://www.pisavisionlab.org/2019/12/30/development-of-context-dependency-in-human-space-perceptionexp-brain-res/https://www.pisavisionlab.org/2019/12/30/motor-commands-induce-time-compression-for-tactile-stimulij-neurosci-27-34-9164-9172/https://www.pisavisionlab.org/2019/12/30/crossing-the-line-estimations-of-line-length-in-the-oppel-kundt-illusionj-vis-8-14/https://www.pisavisionlab.org/2019/12/30/nteraction-between-eye-movements-and-vision-perception-during-saccades-in-j-s-w-l-m-chalupa-ed-the-new-visual-neuroscience-2nd-ed-pp-947-962-mit-press/https://www.pisavisionlab.org/2019/12/30/cerebral-lateralization-for-language-in-deaf-children-with-cochlear-implantationbrain-lang-129-1-6/https://www.pisavisionlab.org/2019/12/29/visual-mislocalization-during-saccade-sequencesexp-brain-res-2-233-577-585/https://www.pisavisionlab.org/2019/12/29/bold-response-selective-to-flow-motion-in-very-young-infants-plos-biol-9-13-e1002260/https://www.pisavisionlab.org/2019/12/29/pattern-recognition-with-adaptive-thresholds-for-sleep-spindle-in-high-density-eeg-signals-paper-presented-at-the-engineering-in-medicine-and-biology-society-embc-2015-37th-annual-international-co/https://www.pisavisionlab.org/2019/12/29/children-with-autism-spectrum-disorder-show-reduced-adaptation-to-numberproceedings-of-the-national-academy-of-sciences-11225-7868-7872/https://www.pisavisionlab.org/2019/12/29/a-low-cost-and-versatile-system-for-projecting-wide-field-visual-stimuli-within-fmri-scannersbehav-res-methods/https://www.pisavisionlab.org/2019/12/29/rhythmic-oscillations-of-visual-contrast-sensitivity-synchronized-with-actionj-neurosci-18-35-7019-7029/https://www.pisavisionlab.org/2019/12/29/inefficient-stimulus-processing-at-encoding-affects-formation-of-high-order-general-representation-a-study-on-cross-modal-word-stem-completion-task-brain-res-1622-386-396/https://www.pisavisionlab.org/2019/12/29/looking-for-a-precursor-of-spontaneous-sleep-slow-oscillations-in-human-sleep-the-role-of-the-sigma-activity-int-j-psychophysiol-2-97-99-107/https://www.pisavisionlab.org/2019/12/29/time-number-and-attention-in-very-low-birth-weight-childrenneuropsychologia-2015/https://www.pisavisionlab.org/2019/12/29/nonretinotopic-visual-processing-in-the-brainvis-neurosci-32-e017/https://www.pisavisionlab.org/2019/12/29/numerical-estimation-in-children-with-autismautism-res/https://www.pisavisionlab.org/2019/12/29/atypicalities-in-perceptual-adaptation-in-autism-do-not-extend-to-perceptual-causalityplos-one-3-10-e0120439/https://www.pisavisionlab.org/2019/12/29/visuotactile-temporal-recalibration-transfers-across-different-locations-multisensory-research-3-4-28-351-370/https://www.pisavisionlab.org/2019/12/29/selective-attention-modulates-early-human-evoked-potentials-during-emotional-face-voice-processing-journal-of-cognitive-neuroscience-4-27-798-818/https://www.pisavisionlab.org/2019/12/28/intonation-processing-deficits-of-emotional-words-among-mandarin-chinese-speakers-with-congenital-amusia-an-erp-study-frontiers-in-psychology-6/https://www.pisavisionlab.org/2019/12/28/effects-of-adaptation-on-numerosity-decoding-in-the-human-brain-neuroimage-143-364-377/https://www.pisavisionlab.org/2019/12/28/different-coding-strategies-for-the-perception-of-stable-and-changeable-facial-attributes-sci-rep-6/https://www.pisavisionlab.org/2019/12/28/an-orientation-dependent-size-illusion-is-underpinned-by-processing-in-the-extrastriate-visual-area-lo1-i-perception-5-7/https://www.pisavisionlab.org/2019/12/28/numerosity-but-not-texture-density-discrimination-correlates-with-math-ability-in-children-dev-psychol-8-52-1206-1216/https://www.pisavisionlab.org/2019/12/28/adaptation-to-numerosity-requires-only-brief-exposures-and-is-determined-by-number-of-events-not-exposure-duration-j-vis-10-16-22/https://www.pisavisionlab.org/2019/12/28/a-shared-numerical-representation-for-action-and-perception-elife-5/https://www.pisavisionlab.org/2019/12/28/perceived-visual-time-depends-on-motor-preparation-and-direction-of-hand-movements-sci-rep-6-27947/https://www.pisavisionlab.org/2019/12/28/early-visual-deprivation-severely-compromises-the-auditory-sense-of-space-in-congenitally-blind-children-dev-psychol-6-52-847-853/https://www.pisavisionlab.org/2019/12/28/adaptation-to-size-affects-saccades-with-long-but-not-short-latencies-j-vis-7-16-2/https://www.pisavisionlab.org/2019/12/28/brain-connectivity-is-altered-by-extreme-physical-exercise-during-non-rem-sleep-and-wakefulness-indications-from-eeg-and-fmri-studies-archives-italiennes-de-biologie-4-154-103-117/https://www.pisavisionlab.org/2019/12/28/rhythmic-modulation-of-visual-contrast-discrimination-triggered-by-action-proceedings-of-the-royal-society-of-london-b-biological-sciences-1831-283/https://www.pisavisionlab.org/2019/12/28/adaptation-induced-compression-of-event-time-occurs-only-for-translational-motion-scientific-reports-6-23341/https://www.pisavisionlab.org/2019/12/28/no-rapid-audiovisual-recalibration-in-adults-on-the-autism-spectrum-scientific-reports-6-21756/https://www.pisavisionlab.org/2019/12/28/visual-plasticity-blindsight-bridges-anatomy-and-function-in-the-visual-system-curr-biol-2-26-r70-73/https://www.pisavisionlab.org/2019/12/28/the-influence-of-visual-information-on-auditory-processing-in-individuals-with-congenital-amusia-an-erp-study-neuroimage-135-142-151/https://www.pisavisionlab.org/2019/12/28/predictive-coding-of-multisensory-timing-current-opinion-in-behavioral-sciences-8-200-206/https://www.pisavisionlab.org/2019/12/28/spatial-but-not-temporal-numerosity-thresholds-correlate-with-formal-math-skills-in-children-dev-psychol/https://www.pisavisionlab.org/2019/12/28/different-responses-of-spontaneous-and-stimulus-related-alpha-activity-to-ambient-luminance-changes-eur-j-neurosci/https://www.pisavisionlab.org/2019/12/28/connecting-visual-objects-reduces-perceived-numerosity-and-density-for-sparse-but-not-dense-patterns-journal-of-numerical-cognition-4-3-2/https://www.pisavisionlab.org/2019/12/28/plasticity-of-the-human-visual-brain-after-an-early-cortical-lesion-neuropsychologia/https://www.pisavisionlab.org/2019/12/28/auditory-sensitivity-and-decision-criteria-oscillate-at-different-frequencies-separately-for-the-two-ears-current-biology/https://www.pisavisionlab.org/2019/12/28/spatial-localization-of-sound-elicits-early-responses-from-occipital-visual-cortex-in-humans-sci-rep-1-7-10415/https://www.pisavisionlab.org/2019/12/27/area-prostriata-in-the-human-brain-curr-biol-19-27-3056-3060-e3053/https://www.pisavisionlab.org/2019/12/27/evidence-for-a-number-sense-perceiving-numerosity-from-birth-behavioral-and-brain-sciences-40-21-22/https://www.pisavisionlab.org/2019/12/27/evidence-for-a-number-sense-behavioral-and-brain-sciences-40-18-19/https://www.pisavisionlab.org/2019/12/27/autism-is-associated-with-reduced-ability-to-interpret-grasping-actions-of-others-sci-rep-1-7-12687/https://www.pisavisionlab.org/2019/12/27/temporally-evolving-gain-mechanisms-of-attention-in-macaque-area-v4-j-neurophysiol-jn-00522-02016/https://www.pisavisionlab.org/2019/12/27/the-light-from-above-prior-is-intact-in-autistic-children-j-exp-child-psychol-161-113-125/https://www.pisavisionlab.org/2019/12/27/hemispheric-language-organization-after-congenital-left-brain-lesions-a-comparison-between-functional-transcranial-doppler-and-functional-mri-j-neuropsychol/https://www.pisavisionlab.org/2019/12/27/audio-visual-temporal-perception-in-children-with-restored-hearing-neuropsychologia-99-350-359/https://www.pisavisionlab.org/2019/12/27/active-vision-dynamic-reformatting-of-visual-information-by-the-saccade-drift-cycle-curr-biol-9-27-r341-r344/https://www.pisavisionlab.org/2019/12/27/spatiotopic-coding-during-dynamic-head-tilt-j-neurophysiol-2-117-808-817/https://www.pisavisionlab.org/2019/12/27/psychophysical-evidence-for-the-number-sense-philos-trans-r-soc-lond-b-biol-sci-1740-373/https://www.pisavisionlab.org/2019/12/27/pitch-discrimination-associated-with-phonological-awareness-evidence-from-congenital-amusia-scientific-reports-1-7/https://www.pisavisionlab.org/2019/12/27/pitch-contour-impairment-in-congenital-amusia-new-insights-from-the-self-paced-audio-visual-contour-task-sact-plos-one-6-12-e0179252/https://www.pisavisionlab.org/2019/12/27/a-matched-comparison-across-three-different-sensory-pairs-of-cross-modal-temporal-recalibration-from-sustained-and-transient-adaptation-i-perception-4-8-204166951771869/https://www.pisavisionlab.org/2019/12/27/visual-information-from-observing-grasping-movement-in-allocentric-and-egocentric-perspectives-development-in-typical-children-exp-brain-res/https://www.pisavisionlab.org/2019/12/27/saccadic-suppression-is-embedded-within-extended-oscillatory-modulation-of-sensitivity-j-neurosci/https://www.pisavisionlab.org/2019/12/27/plasticity-of-visual-pathways-and-function-in-the-developing-brain-is-the-pulvinar-a-crucial-player-front-syst-neurosci-11-3/https://www.pisavisionlab.org/2019/12/27/nsemble-perception-of-emotions-in-autistic-and-typical-children-and-adolescents-developmental-cognitive-neuroscience-24-51-62/https://www.pisavisionlab.org/2019/12/27/distinct-neural-signatures-for-very-small-and-very-large-numerosities-frontiers-in-human-neuroscience-11/https://www.pisavisionlab.org/2019/12/27/rhythmic-motor-behaviour-influences-perception-of-visual-time-proc-biol-sci-1888-285/https://www.pisavisionlab.org/2019/12/27/motion-induced-compression-of-perceived-numerosity-sci-rep-1-8-6966/https://www.pisavisionlab.org/2019/12/27/temporal-coding-of-visual-space-trends-in-cognitive-sciences-10-22-883-895/https://www.pisavisionlab.org/2019/12/27/simultaneous-and-sequential-subitizing-are-separate-systems-and-neither-predicts-math-abilities-journal-of-experimental-child-psychology-178-86-103-2/https://www.pisavisionlab.org/2019/12/27/cognitive-processes-underlying-arithmetical-skills-in-primary-school-the-role-of-fluency-handwriting-number-line-and-number-acuity-neuropsy-trends-23/https://www.pisavisionlab.org/2019/12/27/independent-adaptation-mechanisms-for-numerosity-and-size-perception-provide-evidence-against-a-common-sense-of-magnitude-sci-rep-1-8-13571/https://www.pisavisionlab.org/2019/12/27/perceptual-oscillation-of-audiovisual-time-simultaneity-eneuro-3-5/https://www.pisavisionlab.org/2019/12/27/cortical-bold-responses-to-moderate-and-high-speed-motion-in-the-human-visual-cortex-sci-rep-1-8-8357/https://www.pisavisionlab.org/2019/12/27/syntactic-processing-in-music-and-language-parallel-abnormalities-observed-in-congenital-amusia-neuroimage-clinical-19-640-651/https://www.pisavisionlab.org/2019/12/27/visual-perception-to-curve-or-not-to-curve-current-biology-4-28-r150-r152/https://www.pisavisionlab.org/2019/12/27/past-visual-experiences-weigh-in-on-body-size-estimation-scientific-reports-1-8/https://www.pisavisionlab.org/2019/12/27/visual-sensitivity-and-bias-oscillate-phase-locked-to-saccadic-eye-movements-journal-of-vision-14-19-15/https://www.pisavisionlab.org/2019/12/27/distortions-of-visual-time-induced-by-motor-adaptation-journal-of-experimental-psychology-general/https://www.pisavisionlab.org/2019/12/27/attraction-to-the-recent-past-in-aesthetic-judgments-a-positive-serial-dependence-for-rating-artwork-journal-of-vision-12-19-19/https://www.pisavisionlab.org/2019/12/26/higher-attentional-costs-for-numerosity-estimation-at-high-densities-attention-perception-psychophysics-2/https://www.pisavisionlab.org/2019/12/26/cue-combination-within-a-bayesian-framework-in-multisensory-processes-the-auditory-perspective/https://www.pisavisionlab.org/2019/12/26/simultaneous-and-sequential-subitizing-are-separate-systems-and-neither-predicts-math-abilities-journal-of-experimental-child-psychology-178-86-103/https://www.pisavisionlab.org/2019/12/26/number-cognition-cortex-114-1-4/https://www.pisavisionlab.org/2019/12/26/behavioural-oscillations-in-visual-orientation-discrimination-reveal-distinct-modulation-rates-for-both-sensitivity-and-response-bias-sci-rep-1-9-1115/https://www.pisavisionlab.org/2019/12/26/time-dilation-effect-in-an-active-observer-and-virtual-environment-requires-apparent-motion-no-dilation-for-retinal-or-world-motion-alone-journal-of-vision-193-4/https://www.pisavisionlab.org/2019/12/26/head-movements-modulate-visual-responsiveness-in-the-absence-of-gaze-shiftsneuroreport-8-19-831-834/https://www.pisavisionlab.org/2019/12/26/temporal-mechanisms-of-multimodal-bindingproc-biol-sci-1663-276-1761-1769/https://www.pisavisionlab.org/2019/12/26/shifts-in-spatial-attention-affect-the-perceived-duration-of-eventsj-vis-1-9-9-1-13/https://www.pisavisionlab.org/2019/12/26/spatial-maps-for-time-and-motionexp-brain-res-2-206-121-128/https://www.pisavisionlab.org/2019/12/26/spatiotopic-selectivity-of-adaptation-based-compression-of-event-duration-j-vis-2-11-21-author-reply-21a/https://www.pisavisionlab.org/2019/12/26/blindsight-in-children-with-congenital-and-acquired-cerebral-lesions-cortex-published-online-10-august-2012/https://www.pisavisionlab.org/2019/12/26/the-effects-of-cross-sensory-attentional-demand-on-subitizing-and-on-mapping-number-onto-spacevision-res/https://www.pisavisionlab.org/2019/12/26/perception-of-duration-in-the-parvocellular-system-front-integr-neurosci-614/https://www.pisavisionlab.org/2019/12/26/non-retinotopic-processing-in-ternus-motion-displays-modeled-by-spatiotemporal-filtersj-vis-1-12/https://www.pisavisionlab.org/2019/12/26/optimal-encoding-of-interval-timing-in-expert-percussionists-j-neurosci-3-32-1056-1060/https://www.pisavisionlab.org/2019/12/26/linear-mapping-of-numbers-onto-space-requires-attentioncognition-3-122-454-459/https://www.pisavisionlab.org/2019/12/26/spatiotemporal-filtering-and-motion-illusions-journal-of-vision-1310-21/https://www.pisavisionlab.org/2019/12/26/neon-color-spreading-in-dynamic-displays-temporal-factors-journal-of-vision-13122/https://www.pisavisionlab.org/2019/12/26/whats-up-working-memory-contents-can-bias-orientation-processing-vision-res-76-46-55/https://www.pisavisionlab.org/2019/12/26/vision-efficient-adaptive-codingcurr-biol-22-24-r1096-1098/https://www.pisavisionlab.org/2019/12/26/separate-mechanisms-for-perception-of-numerosity-and-densitypsychol-sci-1-25-265-270/https://www.pisavisionlab.org/2019/12/26/compressive-mapping-of-number-to-space-reflects-dynamic-encoding-mechanisms-not-static-logarithmic-transformproc-natl-acad-sci-u-s-a-21-111-7867-7872/https://www.pisavisionlab.org/2019/12/24/on-the-possibility-of-a-unifying-framework-for-serial-dependencies-i-perception-66-1-16-2/https://www.pisavisionlab.org/2019/12/24/number-as-a-primary-perceptual-attribute-a-review-perception-1-27-doi-10-1177-0301006615602599/https://www.pisavisionlab.org/2019/12/24/the-oblique-effect-is-both-allocentric-and-egocentricjournal-of-vision-8-15-24-24/https://www.pisavisionlab.org/2019/12/24/strong-motion-deficits-in-dyslexia-associated-with-dcdc2-gene-alterationj-neurosci-21-35-8059-8064/https://www.pisavisionlab.org/2019/12/24/mechanisms-for-perception-of-numerosity-or-texture-density-are-governed-by-crowding-like-effectsjournal-of-vision-155-1-12/https://www.pisavisionlab.org/2019/12/24/on-the-possibility-of-a-unifying-framework-for-serial-dependencies-i-perception-66-1-16/https://www.pisavisionlab.org/2019/12/24/visual-bold-response-in-late-blind-subjects-with-argus-ii-retinal-prosthesis-plos-biol-10-14-e1002569/https://www.pisavisionlab.org/2019/12/24/spontaneous-perception-of-numerosity-in-humans-nat-commun-7-12536/https://www.pisavisionlab.org/2019/12/24/central-tendency-effects-in-time-interval-reproduction-in-autism-sci-rep-6-28570/https://www.pisavisionlab.org/2019/12/24/adaptation-to-number-operates-on-perceived-rather-than-physical-numerosity-cognition-151-63-67/https://www.pisavisionlab.org/2019/12/24/multiple-channels-of-visual-time-perception-current-opinion-in-behavioral-sciences-8-131-139/https://www.pisavisionlab.org/2019/12/24/serial-dependencies-act-directly-on-perception-j-vis-14-17-6/https://www.pisavisionlab.org/2019/12/24/serial-effects-are-optimal-behavioral-and-brain-sciences-41/https://www.pisavisionlab.org/2019/12/24/inhibitory-surrounds-of-motion-mechanisms-revealed-by-continuous-tracking-j-vis-13-18-7/https://www.pisavisionlab.org/2019/12/24/typical-numerosity-adaptation-despite-selectively-impaired-number-acuity-in-dyscalculia-neuropsychologia/https://www.pisavisionlab.org/2019/12/24/the-functional-role-of-serial-dependence-proceedings-of-the-royal-society-of-london-b/https://www.pisavisionlab.org/2019/12/24/supramodal-agnosia-for-oblique-mirror-orientation-in-patients-with-periventricular-leukomalacia-cortex/https://www.pisavisionlab.org/2019/12/24/three-systems-for-visual-numerosity-a-single-case-study-neuropsychologia-136-107259/https://www.pisavisionlab.org/2019/12/24/near-optimal-encoding-of-numerosity-in-typical-and-dyscalculic-development-cortex-120-498-508/https://www.pisavisionlab.org/2019/12/24/different-reaction-times-for-subitizing-estimation-and-texture-journal-of-vision-6-19-14/https://www.pisavisionlab.org/2019/12/24/spontaneous-representation-of-numerosity-in-typical-and-dyscalculic-development-cortex-https-doi-org-10-1016-j-cortex-2018-11-019/https://www.pisavisionlab.org/2019/12/24/spontaneous-perception-of-numerosity-in-pre-school-children-proceedings-of-the-royal-society-b-biological-sciences-1906-286-20191245/https://www.pisavisionlab.org/2019/12/23/residual-visual-responses-in-patients-with-retinitis-pigmentosa-revealed-by-functional-magnetic-resonance-imaging-translational-vision-science-technology-6-8-44/https://www.pisavisionlab.org/2019/12/23/brief-periods-of-monocular-deprivation-disrupt-ocular-balance-in-human-adult-visual-cortex-curr-biol-2011-jul-262114r538-9/https://www.pisavisionlab.org/2019/12/23/touch-influences-visual-perception-with-a-tight-orientation-tuningplos-one-11-8-e79558/https://www.pisavisionlab.org/2019/12/23/early-interaction-between-vision-and-touch-during-binocular-rivalrymultisens-res-3-26-291-306/https://www.pisavisionlab.org/2019/12/23/long-term-effects-of-monocular-deprivation-revealed-with-binocular-rivalry-gratings-modulated-in-luminance-and-in-colorj-vis-6-13/https://www.pisavisionlab.org/2019/12/23/touch-interacts-with-vision-during-binocular-rivalry-with-a-tight-orientation-tuningplos-one-3-8-e58754/https://www.pisavisionlab.org/2019/12/23/auditory-and-tactile-signals-combine-to-influence-vision-during-binocular-rivalryj-neurosci-3-34-784-792/https://www.pisavisionlab.org/2019/12/23/a-cycling-lane-for-brain-rewiring-curr-biol-23-25-r1122-r1123/https://www.pisavisionlab.org/2019/12/23/short-term-monocular-deprivation-alters-early-components-of-visual-evoked-potentials-j-physiol-19-593-4361-4372/https://www.pisavisionlab.org/2019/12/23/short-term-monocular-deprivation-alters-gaba-in-the-adult-human-visual-cortexcurr-biol-11-25-1496-1501/https://www.pisavisionlab.org/2019/12/23/congruent-tactile-stimulation-reduces-the-strength-of-visual-suppression-during-binocular-rivalrysci-rep-5/https://www.pisavisionlab.org/2019/12/23/the-temporal-frequency-tuning-of-continuous-flash-suppression-reveals-peak-suppression-at-very-low-frequencies-sci-rep-6-35723/https://www.pisavisionlab.org/2019/12/23/early-cross-modal-plasticity-in-adults-j-cogn-neurosci-3-29-520-529/https://www.pisavisionlab.org/2019/12/23/binocular-rivalry-measured-2-hours-after-occlusion-therapy-predicts-the-recovery-rate-of-the-amblyopic-eye-in-anisometropic-children-invest-ophthalmol-vis-sci-4-57-1537-1546/https://www.pisavisionlab.org/2019/12/23/the-complex-interplay-between-multisensory-integration-and-perceptual-awareness-multisensory-research/https://www.pisavisionlab.org/2019/12/23/consciousness-is-more-than-meets-the-eye-a-call-for-a-multisensory-study-of-subjective-experience-neuroscience-of-consciousness-1-8/https://www.pisavisionlab.org/2019/12/23/touch-accelerates-visual-awareness-iperception-1-8-2041669516686986/https://www.pisavisionlab.org/2019/12/23/binocular-rivalry-in-children-on-the-autism-spectrum-autism-res/https://www.pisavisionlab.org/2019/12/22/a-new-counterintuitive-training-for-adult-amblyopia-annals-of-clinical-and-translational-neurology/https://www.pisavisionlab.org/2019/12/22/categorical-perception-of-newly-learned-facesvisual-cognition-4-15-420-467/https://www.pisavisionlab.org/2019/12/22/fusion-of-visual-and-auditory-stimuli-during-saccades-a-bayesian-explanation-for-perisaccadic-distortionsj-neurosci-32-27-8525-8532/https://www.pisavisionlab.org/2019/12/22/spatiotemporal-distortions-of-visual-perception-at-the-time-of-saccadesj-neurosci-42-29-13147-13157/https://www.pisavisionlab.org/2019/12/22/temporal-auditory-capture-does-not-affect-the-time-course-of-saccadic-mislocalization-of-visual-stimulij-vis-2-10-7-1-13/https://www.pisavisionlab.org/2019/12/22/saccades-compress-space-time-and-numbertrends-cogn-sci-12-14-528-533/https://www.pisavisionlab.org/2019/12/22/touch-disambiguates-rivalrous-perception-at-early-stages-of-visual-analysiscurr-biol-4-20-r143-144/https://www.pisavisionlab.org/2019/12/22/spatiotemporal-profile-of-peri-saccadic-contrast-sensitivityj-vis-14-11/https://www.pisavisionlab.org/2019/12/22/underestimation-of-perceived-number-at-the-time-of-saccadesvision-res-1-51-34-42/https://www.pisavisionlab.org/2019/12/22/saccadic-compression-of-symbolic-numerical-magnitudeplos-one-11-7-e49587/https://www.pisavisionlab.org/2019/12/22/pupil-constrictions-to-photographs-of-the-sunjournal-of-vision-6-13/https://www.pisavisionlab.org/2019/12/22/attention-to-bright-surfaces-enhances-the-pupillary-light-reflexj-neurosci-5-33-2199-2204/https://www.pisavisionlab.org/2019/12/22/attention-to-bright-surfaces-enhances-the-pupillary-light-reflexjournal-of-neuroscience-5-33-2199-2204/https://www.pisavisionlab.org/2019/12/22/transient-spatiotopic-integration-across-saccadic-eye-movements-mediates-visual-stabilityj-neurophysiol-4-109-1117-1125/https://www.pisavisionlab.org/2019/12/22/pupil-size-reflects-the-focus-of-feature-based-attentionjournal-of-neurophysiology-12-112-3046-3052/https://www.pisavisionlab.org/2019/12/22/effect-of-saccade-automaticity-on-perisaccadic-space-compression-front-syst-neurosci-9-127/https://www.pisavisionlab.org/2019/12/22/resting-state-retinotopic-organization-in-the-absence-of-retinal-input-and-visual-experiencej-neurosci-36-35-12366-12382/https://www.pisavisionlab.org/2019/12/22/introduction-to-the-special-issue-on-multimodality-of-early-sensory-processing-early-visual-maps-flexibly-encode-multimodal-space-multisensory-research-3-4-28-249-252/https://www.pisavisionlab.org/2019/12/22/spatial-attention-increases-the-pupillary-response-to-light-changesj-vis-2-15-1/https://www.pisavisionlab.org/2019/12/22/keeping-a-large-pupilled-eye-on-high-level-visual-processingtrends-cogn-sci/https://www.pisavisionlab.org/2019/12/22/dissociable-saccadic-suppression-of-pupillary-and-perceptual-responses-to-light-j-neurophysiol-3-115-1243-1251/https://www.pisavisionlab.org/2019/12/22/pupil-response-components-attention-light-interaction-in-patients-with-parinauds-syndrome-sci-rep-1-7-10283/https://www.pisavisionlab.org/2019/12/22/renewed-attention-on-the-pupil-light-reflex-trends-neurosci/https://www.pisavisionlab.org/2019/12/22/short-term-monocular-deprivation-enhances-physiological-pupillary-oscillations-neural-plast-2017-6724631/https://www.pisavisionlab.org/2019/12/22/response-to-short-term-deprivation-of-the-human-adult-visual-cortex-measured-with-7t-bold-elife-7/https://www.pisavisionlab.org/2019/12/22/pupil-size-as-a-gateway-into-conscious-interpretation-of-brightness-frontiers-in-neurology-9/https://www.pisavisionlab.org/2019/12/22/vision-during-saccadic-eye-movements-annual-review-of-vision-science-1-4-193-213/https://www.pisavisionlab.org/2019/12/22/trans-saccadic-integration-of-orientation-information-j-vis-4-18-9/https://www.pisavisionlab.org/2019/12/22/pupillometry-reveals-perceptual-differences-that-are-tightly-linked-to-autistic-traits-in-typical-adults-elife-7/https://www.pisavisionlab.org/2019/11/28/perception-during-double-step-saccades-sci-rep-1-8-320/https://www.pisavisionlab.org/2019/11/28/exenatide-modulates-visual-cortex-responses-diabetes-metab-res-rev-e3167/https://www.pisavisionlab.org/2019/11/28/908-2/https://www.pisavisionlab.org/2014/08/24/new-research-published-on-behavioral-and-brain-sciences/