5 results match your criteria: "University of Helsinki and Helsinki University HospitalHelsinki[Affiliation]"

Neuropathic pain caused by nerve damage is a common and severe class of chronic pain. Disease-modifying clinical therapies are needed as current treatments typically provide only symptomatic relief; show varying clinical efficacy; and most have significant adverse effects. One approach is targeting either neurotrophic factors or their receptors that normalize sensory neuron function and stimulate regeneration after nerve damage.

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Children born extremely preterm (EPT) may have difficulties in response inhibition, but the neural basis of such problems is unknown. We recorded magnetoencephalography (MEG) during a somatosensory Go/NoGo task in 6-year-old children born EPT ( = 22) and in children born full term (FT; = 21). The children received tactile stimuli randomly to their left little (target) and index (non-target) finger and were instructed to squeeze a soft toy with the opposite hand every time they felt a stimulus on the little finger.

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Article Synopsis
  • In spinal paired associative stimulation (PAS), the timing of transcranial magnetic stimulation (TMS) and peripheral nerve stimulation (PNS) affects whether motor-evoked potentials (MEPs) increase or decrease.
  • A new PAS protocol using high-intensity TMS and high-frequency PNS was successful in inducing MEP potentiation across various interstimulus intervals (ISIs) in all tested subjects.
  • This modified PAS approach could be a promising long-term rehabilitation strategy for neurological patients without needing precise ISI adjustments.
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In the visual cortex, stimuli outside the classical receptive field (CRF) modulate the neural firing rate, without driving the neuron by themselves. In the primary visual cortex (V1), such contextual modulation can be parametrized with an area summation function (ASF): increasing stimulus size causes first an increase and then a decrease of firing rate before reaching an asymptote. Earlier work has reported increase of sparseness when CRF stimulation is extended to its surroundings.

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