<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns="http://purl.org/rss/1.0/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/">
<channel rdf:about="https://hdl.handle.net/20.500.11811/819">
<title>Klinik für Epileptologie</title>
<link>https://hdl.handle.net/20.500.11811/819</link>
<description/>
<items>
<rdf:Seq>
<rdf:li rdf:resource="https://hdl.handle.net/20.500.11811/13325"/>
<rdf:li rdf:resource="https://hdl.handle.net/20.500.11811/13318"/>
<rdf:li rdf:resource="https://hdl.handle.net/20.500.11811/13253"/>
<rdf:li rdf:resource="https://hdl.handle.net/20.500.11811/12938"/>
</rdf:Seq>
</items>
<dc:date>2026-04-10T21:49:08Z</dc:date>
</channel>
<item rdf:about="https://hdl.handle.net/20.500.11811/13325">
<title>Single-neuron representations of odours in the human brain</title>
<link>https://hdl.handle.net/20.500.11811/13325</link>
<description>Single-neuron representations of odours in the human brain
Kehl, Marcel S.; Mackay, Sina; Ohla, Kathrin; Schneider, Matthias; Borger, Valeri; Surges, Rainer; Spehr, Marc; Mormann, Florian
Olfaction is a fundamental sensory modality that guides animal and human behaviour. However, the underlying neural processes of human olfaction are still poorly understood at the fundamental—that is, the single-neuron—level. Here we report recordings of single-neuron activity in the piriform cortex and medial temporal lobe in awake humans performing an odour rating and identification task. We identified odour-modulated neurons within the piriform cortex, amygdala, entorhinal cortex and hippocampus. In each of these regions, neuronal firing accurately encodes odour identity. Notably, repeated odour presentations reduce response firing rates, demonstrating central repetition suppression and habituation. Different medial temporal lobe regions have distinct roles in odour processing, with amygdala neurons encoding subjective odour valence, and hippocampal neurons predicting behavioural odour identification performance. Whereas piriform neurons preferably encode chemical odour identity, hippocampal activity reflects subjective odour perception. Critically, we identify that piriform cortex neurons reliably encode odour-related images, supporting a multimodal role of the human piriform cortex. We also observe marked cross-modal coding of both odours and images, especially in the amygdala and piriform cortex. Moreover, we identify neurons that respond to semantically coherent odour and image information, demonstrating conceptual coding schemes in olfaction. Our results bridge the long-standing gap between animal models and non-invasive human studies and advance our understanding of odour processing in the human brain by identifying neuronal odour-coding principles, regional functional differences and cross-modal integration.
</description>
<dc:date>2024-10-09T00:00:00Z</dc:date>
</item>
<item rdf:about="https://hdl.handle.net/20.500.11811/13318">
<title>Mind wandering, poor sleep, and negative affect: a threefold vicious cycle?</title>
<link>https://hdl.handle.net/20.500.11811/13318</link>
<description>Mind wandering, poor sleep, and negative affect: a threefold vicious cycle?
Fell, Juergen
Mind wandering (MW) is intricately linked to sleep and affect, bearing clinical relevance for various psychiatric conditions, notably attention deficit/hyperactivity disorder, depression, and anxiety disorders. Most reviews concur that the relationship between disturbed sleep and negative affect is bidirectional. The directional relationships between MW propensity and disturbed sleep, as well as MW propensity and negative affect, are less clear. Therefore, this brief review aims to examine the limited studies that have directly explored temporally sequential relationships. These studies provide clear evidence for an impact of affect on MW and of MW on sleep, along with less unequivocal evidence for an influence of MW on affect and sleep on MW. Collectively, these individual reinforcement loops may constitute a threefold vicious cycle, which may contribute to the development and perpetuation of psychiatric disorders. Available data convincingly suggest an impact cycle in the direction "MW propensity → disturbed sleep → negative affect → MW propensity," while evidence for the inverse impact cycle is less pronounced.
</description>
<dc:date>2024-09-05T00:00:00Z</dc:date>
</item>
<item rdf:about="https://hdl.handle.net/20.500.11811/13253">
<title>Long-term seizure outcome after epilepsy surgery of neuroglial tumors</title>
<link>https://hdl.handle.net/20.500.11811/13253</link>
<description>Long-term seizure outcome after epilepsy surgery of neuroglial tumors
Rácz, Attila; Müller, Philipp; Becker, Albert; Hoffmann, Nico; Rüber, Theodor; Borger, Valeri; Vatter, Hartmut; Surges, Rainer; Elger, Christian E.
&lt;strong&gt;Purpose:&lt;/strong&gt; Neuroglial tumors are frequently associated with pharmacorefractory epilepsies. However, comprehensive knowledge about long-term outcomes after epilepsy surgery and the main prognostic factors for outcome is still limited. We sought to evaluate long-term outcomes and potential influencing factors in a large cohort of patients who underwent surgery for neuroglial tumors in a single-center setting.&lt;br /&gt; &lt;strong&gt;Methods:&lt;/strong&gt; The study analyzed the outcomes of 107 patients who underwent epilepsy surgery for neuroglial tumors between 2001 and 2020 at the Department of Epileptology, University Hospital Bonn, in Germany. The outcomes were evaluated using Engel classification. Differences in outcome related to potential prognostic factors were examined using the Chi2-test, Fisher's exact test and sign test. Additionally, stepwise logistic regression analysis was employed to identify independent prognostic factors.&lt;br /&gt; &lt;strong&gt;Results:&lt;/strong&gt; Complete seizure freedom (Engel Class IA) was achieved in 75% of the operated patients at 12 months, and 56% at the last follow-up visit (70.4 ± 6.2 months, median: 40 months). Completeness of resection was a crucial factor for both 12-month follow-up outcomes and the longest available outcomes, whereas lobar tumor localization, histology (ganglioglioma vs. dysembryoplastic neuroepithelial tumor), history of bilateral tonic–clonic seizures prior to surgery, invasive diagnostics, side of surgery (dominant vs. non-dominant hemisphere), age at epilepsy onset, age at surgery, and epilepsy duration did not consistently impact postsurgical outcomes. Among temporal lobe surgeries, patients who underwent lesionectomy and lesionectomy, including hippocampal resection, demonstrated similar outcomes.&lt;br /&gt; &lt;strong&gt;Conclusion:&lt;/strong&gt; Neuroglial tumors present as excellent surgical substrates in treating structural epilepsy. To achieve an optimal postsurgical outcome, a complete lesion resection should be pursued whenever possible.
</description>
<dc:date>2024-05-23T00:00:00Z</dc:date>
</item>
<item rdf:about="https://hdl.handle.net/20.500.11811/12938">
<title>Ripple-locked coactivity of stimulus-specific neurons and human associative memory</title>
<link>https://hdl.handle.net/20.500.11811/12938</link>
<description>Ripple-locked coactivity of stimulus-specific neurons and human associative memory
Kunz, Lukas; Staresina, Bernhard P.; Reinacher, Peter C.; Brandt, Armin; Guth, Tim A.; Schulze-Bonhage, Andreas; Jacobs, Joshua
Associative memory enables the encoding and retrieval of relations between different stimuli. To better understand its neural basis, we investigated whether associative memory involves temporally correlated spiking of medial temporal lobe (MTL) neurons that exhibit stimulus-specific tuning. Using single-neuron recordings from patients with epilepsy performing an associative object–location memory task, we identified the object-specific and place-specific neurons that represented the separate elements of each memory. When patients encoded and retrieved particular memories, the relevant object-specific and place-specific neurons activated together during hippocampal ripples. This ripple-locked coactivity of stimulus-specific neurons emerged over time as the patients’ associative learning progressed. Between encoding and retrieval, the ripple-locked timing of coactivity shifted, suggesting flexibility in the interaction between MTL neurons and hippocampal ripples according to behavioral demands. Our results are consistent with a cellular account of associative memory, in which hippocampal ripples coordinate the activity of specialized cellular populations to facilitate links between stimuli.
</description>
<dc:date>2024-02-16T00:00:00Z</dc:date>
</item>
</rdf:RDF>
