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Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Molecular Neurodegeneration
|
August 12, 2021
Microglial inclusions and neurofilament light chain release follow neuronal α-synuclein lesions in long-term brain slice cultures
Melanie Barth, Mehtap Bacioglu, Niklas Schwarz, et al.
The Journal of Clinical Investigation
|
September 21, 2021
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
Eva Auffenberg, Ulrike Bs Hedrich, Raffaella Barbieri, et al.
Journal of Neurophysiology
|
February 27, 2025
Comprehensive analysis of human dendritic spine morphology and density
Kerstin D Schünemann, Roxanne M Hattingh, Matthijs B Verhoog, et al.
The Journal of Clinical Investigation
|
May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Brain : a Journal of Neurology
|
June 26, 2008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
Arvid Suls, Peter Dedeken, Karolien Goffin, et al.
Brain : a Journal of Neurology
|
June 5, 2025
The genetic and phenotypic spectrum of GABRB1-related disorders
Charissa Millevert, Anthony Sze Hon Kan, Moritz Hanke, et al.
Neurology
|
January 6, 2017
Mutations in GABRB3: From febrile seizures to epileptic encephalopathies
Rikke S Møller, Thomas V Wuttke, Ingo Helbig, et al.
Nature Neuroscience
|
August 26, 2020
A community-based transcriptomics classification and nomenclature of neocortical cell types
Rafael Yuste, Michael Hawrylycz, Nadia Aalling, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Molecular Neurodegeneration
|
August 12, 2021
Microglial inclusions and neurofilament light chain release follow neuronal α-synuclein lesions in long-term brain slice cultures
Melanie Barth, Mehtap Bacioglu, Niklas Schwarz, et al.
The Journal of Clinical Investigation
|
September 21, 2021
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
Eva Auffenberg, Ulrike Bs Hedrich, Raffaella Barbieri, et al.
Journal of Neurophysiology
|
February 27, 2025
Comprehensive analysis of human dendritic spine morphology and density
Kerstin D Schünemann, Roxanne M Hattingh, Matthijs B Verhoog, et al.
The Journal of Clinical Investigation
|
May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Brain : a Journal of Neurology
|
June 26, 2008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1
Arvid Suls, Peter Dedeken, Karolien Goffin, et al.
Brain : a Journal of Neurology
|
June 5, 2025
The genetic and phenotypic spectrum of GABRB1-related disorders
Charissa Millevert, Anthony Sze Hon Kan, Moritz Hanke, et al.
Neurology
|
January 6, 2017
Mutations in GABRB3: From febrile seizures to epileptic encephalopathies
Rikke S Møller, Thomas V Wuttke, Ingo Helbig, et al.
Nature Neuroscience
|
August 26, 2020
A community-based transcriptomics classification and nomenclature of neocortical cell types
Rafael Yuste, Michael Hawrylycz, Nadia Aalling, et al.
Page
of 4