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The International Journal of Biochemistry & Cell Biology|December 18, 2018
The paroxysmal depolarization shift in epilepsy researchMatej Hotka, Helmut Kubista
International Journal of Molecular Sciences|February 1, 2019
The Paroxysmal Depolarization Shift: Reconsidering Its Role in Epilepsy, Epileptogenesis and BeyondHelmut Kubista, Stefan Boehm, Matej Hotka
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2022
Glycerol-3-Phosphate Shuttle Is a Backup System Securing Metabolic Flexibility in NeuronsAnkit Dhoundiyal, Vanessa Goeschl, Stefan Boehm, et al.
Neuropharmacology|August 8, 2025
IP<sub>3</sub>-mediated Ca<sup>2+</sup> transfer from ER to mitochondria stimulates ATP synthesis in primary hippocampal neuronsAnkit Dhoundiyal, Vanessa Goeschl, Stefan Boehm, et al.
Epilepsia|March 16, 2017
Ca<sub>v</sub> 1.3 channels play a crucial role in the formation of paroxysmal depolarization shifts in cultured hippocampal neuronsVictoria Stiglbauer, Matej Hotka, Manuel Ruiß, et al.
Science Signaling|February 13, 2020
L-type Ca<sup>2+</sup> channel-mediated Ca<sup>2+</sup> influx adjusts neuronal mitochondrial function to physiological and pathophysiological conditionsMatej Hotka, Michal Cagalinec, Karlheinz Hilber, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 14, 2025
Mitochondrial Glutamine Metabolism Drives Epileptogenesis in Primary Hippocampal NeuronsHelmut Kubista, Francesco Gentile, Klaus Schicker, et al.
Journal of Cell Science|March 16, 2026
αKGDHC activity modulates glutamate excitotoxicity via metabotropic regulation of NMDA receptors in primary culturesVanessa Goeschl, Matej Hotka, Bernhard Hochreiter, et al.
Neuroscience|May 20, 2021
On the Origin of Paroxysmal Depolarization Shifts: The Contribution of Ca<sub>v</sub>1.x Channels as the Common Denominator of a Polymorphous Neuronal Discharge PatternChristiane Meyer, Annika Kettner, Ulla Hochenegg, et al.
Neuropharmacology|March 20, 2019
Rescue by 4-phenylbutyrate of several misfolded creatine transporter-1 variants linked to the creatine transporter deficiency syndromeAli El-Kasaby, Ameya Kasture, Florian Koban, et al.
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