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Annals of Neurology
|
March 21, 2020
Drebrin Autoantibodies in Patients with Seizures and Suspected Encephalitis
Julika Pitsch, Delara Kamalizade, Anna Braun, et al.
Brain : a Journal of Neurology
|
April 8, 2010
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy
Yunxiang Liao, Liesbet Deprez, Snezana Maljevic, et al.
Neurology
|
May 2, 2025
Association of Cortical Atrophy Patterns With Clinical Phenotypes and Histopathological Findings in Patients With Rasmussen Syndrome
Tobias Bauer, Nina R Held, Lennart Walger, et al.
Annals of Neurology
|
December 28, 2020
CD8<sup>+</sup> T-Lymphocyte-Driven Limbic Encephalitis Results in Temporal Lobe Epilepsy
Julika Pitsch, Karen M J van Loo, Marco Gallus, et al.
Annals of Clinical and Translational Neurology
|
November 29, 2021
Impact of T cells on neurodegeneration in anti-GAD65 limbic encephalitis
Andre Dik, Guido Widman, Andreas Schulte-Mecklenbeck, et al.
Journal of Neuroinflammation
|
July 7, 2026
Forkhead box versus NF-κB hippocampal snRNA-seq profiles distinguish anti-Drebrin- and anti-GAD65-positive encephalitis
Karen M J van Loo, Daniel S Galvis-Montes, Annika Breuer, et al.
Science Translational Medicine
|
September 17, 2025
Hippocampal spreading depolarization as a driver of postictal ambulation
Bence Mitlasóczki, Adrián Gutiérrez Gómez, Midia Kamali, et al.
Brain : a Journal of Neurology
|
October 31, 2022
Temporal lobe epilepsy with GAD antibodies: neurons killed by T cells not by complement membrane attack complex
Anna R Tröscher, Katharina M Mair, Laia Verdú de Juan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 6, 2021
A CRISPR-Cas9-engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctions
Miguel Rodríguez de Los Santos, Marion Rivalan, Friederike S David, et al.
Acta Neuropathologica
|
May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
Katri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.
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of 6
Search research articles
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Showing results (41-50 of 52) with videos related to
Sort By:
Page
of 6
Annals of Neurology
|
March 21, 2020
Drebrin Autoantibodies in Patients with Seizures and Suspected Encephalitis
Julika Pitsch, Delara Kamalizade, Anna Braun, et al.
Brain : a Journal of Neurology
|
April 8, 2010
Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy
Yunxiang Liao, Liesbet Deprez, Snezana Maljevic, et al.
Neurology
|
May 2, 2025
Association of Cortical Atrophy Patterns With Clinical Phenotypes and Histopathological Findings in Patients With Rasmussen Syndrome
Tobias Bauer, Nina R Held, Lennart Walger, et al.
Annals of Neurology
|
December 28, 2020
CD8<sup>+</sup> T-Lymphocyte-Driven Limbic Encephalitis Results in Temporal Lobe Epilepsy
Julika Pitsch, Karen M J van Loo, Marco Gallus, et al.
Annals of Clinical and Translational Neurology
|
November 29, 2021
Impact of T cells on neurodegeneration in anti-GAD65 limbic encephalitis
Andre Dik, Guido Widman, Andreas Schulte-Mecklenbeck, et al.
Journal of Neuroinflammation
|
July 7, 2026
Forkhead box versus NF-κB hippocampal snRNA-seq profiles distinguish anti-Drebrin- and anti-GAD65-positive encephalitis
Karen M J van Loo, Daniel S Galvis-Montes, Annika Breuer, et al.
Science Translational Medicine
|
September 17, 2025
Hippocampal spreading depolarization as a driver of postictal ambulation
Bence Mitlasóczki, Adrián Gutiérrez Gómez, Midia Kamali, et al.
Brain : a Journal of Neurology
|
October 31, 2022
Temporal lobe epilepsy with GAD antibodies: neurons killed by T cells not by complement membrane attack complex
Anna R Tröscher, Katharina M Mair, Laia Verdú de Juan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 6, 2021
A CRISPR-Cas9-engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctions
Miguel Rodríguez de Los Santos, Marion Rivalan, Friederike S David, et al.
Acta Neuropathologica
|
May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
Katri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.
Page
of 6