Zobrazeno 1 - 10
of 20
pro vyhledávání: '"pathology [Epilepsy]"'
Autor:
Lukas Henning, Henrike Antony, Annika Breuer, Julia Müller, Gerald Seifert, Etienne Audinat, Parmveer Singh, Frederic Brosseron, Michael T. Heneka, Christian Steinhäuser, Peter Bedner
Publikováno v:
Glia 71(2), 168-186 (2023). doi:10.1002/glia.24265
Extensive microglia reactivity has been well described in human and experimental temporal lobe epilepsy (TLE). To date, however, it is not clear whether and based on which molecular mechanisms microglia contribute to the development and progression o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7febe93f8d8c48e53108d8572a2f2a1d
Autor:
James D. Mills, Eleonora Aronica, Wim Van Hecke, Till S. Zimmer, Stefanie Dedeurwaerdere, Johannes C. Baayen, Sander Idema, Nicole N. van der Wel, Anatoly Korotkov, Jonathan van Eyll, Peter C. van Rijen, Rainer Surges, Erwin A. van Vliet, Helmut W. Kessels, Jan A. Gorter, Diede W. M. Broekaart, Angelika Mühlebner, Martin Schidlowski, Theodor Rüber, Bastian David, Gabriele Ruffolo, Liesbeth François
Publikováno v:
Acta Neuropathologica, 142(4), 729-759. Springer Verlag
Acta neuropathologica 142(4), 729-759 (2021). doi:10.1007/s00401-021-02348-6
Acta neuropathologica, 142(4), 729-759. Springer Verlag
Acta Neuropathologica
Acta neuropathologica 142(4), 729-759 (2021). doi:10.1007/s00401-021-02348-6
Acta neuropathologica, 142(4), 729-759. Springer Verlag
Acta Neuropathologica
Neuronal dysfunction due to iron accumulation in conjunction with reactive oxygen species (ROS) could represent an important, yet underappreciated, component of the epileptogenic process. However, to date, alterations in iron metabolism in the epilep
Autor:
Christian Lavigne, Christoph Kessler, Matthias R. Baumgartner, Patricie Burda, François Feillet, Martina Huemer, Viktor Kožich, Mirian C. H. Janssen, Fanny Mochel, Rebecca Schüle, Pavel Ješina, Karolina M. Stepien, Adeline Regnier, Isabelle Redonnet-Vernhet, Jean-François Benoist, Cecilia Marelli
Publikováno v:
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, Springer Verlag, 2021, 44 (3), pp.777-786. ⟨10.1002/jimd.12323⟩
Journal of Inherited Metabolic Disease, 44, 777-786
Journal of Inherited Metabolic Disease 44(3), 777-786 (2021). doi:10.1002/jimd.12323
Journal of Inherited Metabolic Disease, 44, 3, pp. 777-786
Journal of Inherited Metabolic Disease, Springer Verlag, 2021, 44 (3), pp.777-786. ⟨10.1002/jimd.12323⟩
Journal of Inherited Metabolic Disease, 44, 777-786
Journal of Inherited Metabolic Disease 44(3), 777-786 (2021). doi:10.1002/jimd.12323
Journal of Inherited Metabolic Disease, 44, 3, pp. 777-786
Item does not contain fulltext 5,10-Methylenetetrahydrofolate reductase (MTHFR) deficiency usually presents as a severe neonatal disease. This study aimed to characterize natural history, biological and molecular data, and response to treatment of pa
Autor:
Elodie Chabrol, Roger Prades, Anatoly Korotkov, Oleg Senkov, Shaobo Jia, Johannes C. Baayen, Jan A. Gorter, Diede W. M. Broekaart, Alexander Dityatev, Wytse J. Wadman, Sander Idema, Jasper J. Anink, Alexandra Bertran, Erwin A. van Vliet, Eleonora Aronica, Albert J. Becker, James D. Mills, Jesús Seco, Anika Bongaarts, Teresa Tarragó
Publikováno v:
Journal of Clinical Investigation, 131(1):e138332. The American Society for Clinical Investigation
Broekaart, D W M, Bertran, A, Jia, S, Korotkov, A, Senkov, O, Bongaarts, A, Mills, J D, Anink, J J, Seco, J, Baayen, J C, Idema, S, Chabrol, E, Becker, A J, Wadman, W J, Tarragó, T, Gorter, J A, Aronica, E, Prades, R, Dityatev, A & van Vliet, E A 2021, ' The matrix metalloproteinase inhibitor IPR-179 has antiseizure and antiepileptogenic effects ', Journal of Clinical Investigation, vol. 131, no. 1, e138332 . https://doi.org/10.1172/JCI138332
J Clin Invest
The journal of clinical investigation 131(1), e138332 (2021). doi:10.1172/JCI138332
Journal of clinical investigation, 131(1):e138332. The American Society for Clinical Investigation
The journal of clinical investigation, 131(1):e138332. The American Society for Clinical Investigation
Broekaart, D W M, Bertran, A, Jia, S, Korotkov, A, Senkov, O, Bongaarts, A, Mills, J D, Anink, J J, Seco, J, Baayen, J C, Idema, S, Chabrol, E, Becker, A J, Wadman, W J, Tarragó, T, Gorter, J A, Aronica, E, Prades, R, Dityatev, A & van Vliet, E A 2021, ' The matrix metalloproteinase inhibitor IPR-179 has antiseizure and antiepileptogenic effects ', Journal of Clinical Investigation, vol. 131, no. 1, e138332 . https://doi.org/10.1172/JCI138332
J Clin Invest
The journal of clinical investigation 131(1), e138332 (2021). doi:10.1172/JCI138332
Journal of clinical investigation, 131(1):e138332. The American Society for Clinical Investigation
The journal of clinical investigation, 131(1):e138332. The American Society for Clinical Investigation
Matrix metalloproteinases (MMPs) are synthesized by neurons and glia and released into the extracellular space, where they act as modulators of neuroplasticity and neuroinflammatory agents. Development of epilepsy (epileptogenesis) is associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba82be954946800f57c88d15af875b95
https://research.vumc.nl/en/publications/7ff5ba3a-afb5-4d69-ba8a-c911324843ff
https://research.vumc.nl/en/publications/7ff5ba3a-afb5-4d69-ba8a-c911324843ff
Autor:
Schänzer, Anne, Achleitner, Melanie T., Trümbach, Dietrich, Hubert, Laurence, Munnich, Arnold, Ahlemeyer, Barbara, AlAbdulrahim, Maha M., Greif, Philipp A., Vosberg, Sebastian, Hummer, Blake, Feichtinger, René G., Mayr, Johannes A., Wortmann, Saskia B., Aichner, Heidi, Rudnik-Schöneborn, Sabine, Ruiz, Anna, Gabau, Elisabeth, Sánchez, Jacobo Pérez, Ellard, Sian, Homfray, Tessa, Stals, Karen L., Wurst, Wolfgang, Neubauer, Bernd A., Acker, Till, Bohlander, Stefan K., Asensio, Cédric, Besmond, Claude, Alkuraya, Fowzan S., AlSayed, Moenaldeen D., Hahn, Andreas, Weber, Axel, Justus Liebig University Giessen
Publikováno v:
Annals of neurology 90(1), 143-158 (2021). doi:10.1002/ana.26127
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Ann. Neurol. 90, 143-158 (2021)
Annals of neurology
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Ann. Neurol. 90, 143-158 (2021)
Annals of neurology
Objective Precursors of peptide hormones undergo posttranslational modifications within the trans-Golgi network (TGN). Dysfunction of proteins involved at different steps of this process cause several complex syndromes affecting the central nervous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3330af47383d2432390544a36ec919b7
https://pub.dzne.de/record/155719
https://pub.dzne.de/record/155719
Autor:
Atsushi Nambu, Makoto Sanbo, Xiumin Chen, Yuko Fukata, Harald Prüss, Hans-Christian Kornau, Hiroki Inahashi, Masumi Hirabayashi, Teppei Goto, Roger A. Nicoll, Yoko Hirano, Atsushi Yamagata, Satomi Chiken, Masaki Fukata, Shuya Fukai, Hiromi Sano
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America 118(3), e2022580118-(2021). doi:10.1073/pnas.2022580118
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America
Significance This study addresses a fundamental question in neuroscience, namely how does the presynaptic component of the synapse precisely align with the postsynaptic component? This is essential for the proper transmission of signals across the sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68628950b12bc111c5ad4ecbb0ec6b28
Autor:
Marina Dusl, Thomas Klopstock, Silvia Belia, Manuela Wiessner, Peter Bauer, Jan Senderek, Claudia Stendel, Marta Cenciarini, Ehsan Nematian-Ardestani, Mauro Pessia, Maria Cristina D'Adamo
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 11
International journal of molecular sciences 21(11), 3810-(2020). doi:10.3390/ijms21113810
International Journal of Molecular Sciences, Vol 21, Iss 3810, p 3810 (2020)
Volume 21
Issue 11
International journal of molecular sciences 21(11), 3810-(2020). doi:10.3390/ijms21113810
International Journal of Molecular Sciences, Vol 21, Iss 3810, p 3810 (2020)
Episodic ataxia type 2 (EA2) is characterized by paroxysmal attacks of ataxia with typical onset in childhood or early adolescence. The disease is associated with mutations in the voltage-gated calcium channel alpha 1A subunit (Cav2.1) that is encode
Autor:
Gottfried Schlaug, Guido Lüchters, Bernd Weber, Elke Hattingen, Alon Friedman, Christian E. Elger, Robert D. Nass, Rainer Surges, Bastian David, Tony Stöcker, Theodor Rüber, Ralf Deichmann
Publikováno v:
Brain 141(10), 2952-2965 (2018). doi:10.1093/brain/awy242
Epilepsy has been associated with a dysfunction of the blood-brain barrier. While there is ample evidence that a dysfunction of the blood-brain barrier contributes to epileptogenesis, blood-brain barrier dysfunction as a consequence of single epilept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba31eddcb13958e778b00a300a21d964
https://pub.dzne.de/record/140260
https://pub.dzne.de/record/140260
Autor:
Anton Ivanov, Vu Thao Quyen Le-Schulte, Christophe Bernard, Fabio Morellini, Ronny Eichler, Axel Neu, Stephan Lawrence Marguet, Igor Jakovcevski, Ileana L. Hanganu-Opatz, Dirk Isbrandt, Andrea Merseburg
Publikováno v:
Nature medicine 21(12), 1436-1444 (2015). doi:10.1038/nm.3987
The nervous system is vulnerable to perturbations during specific developmental periods. Insults during such susceptible time windows can have long-term consequences, including the development of neurological diseases such as epilepsy. Here we report
Autor:
Christian Steinhäuser, Michel K. Herde, Martin K. Schwarz, Tingsong Li, Peter Bedner, Tushar Deshpande, Albert J. Becker, Hartmut Vatter, Christian Henneberger
Publikováno v:
Glia 65(11), 1809-1820 (2017). doi:10.1002/glia.23196
Dysfunctional astrocytes are increasingly recognized as key players in the development and progression of mesial temporal lobe epilepsy (MTLE). One of the dramatic changes astrocytes undergo in MTLE with hippocampal sclerosis (HS) is loss of gap junc