Results 251 to 260 of about 2,037,182 (380)

Attenuating midline thalamus bursting to mitigate absence epilepsy. [PDF]

Proc Natl Acad Sci U S A
Dong P, Bakhurin K, Li Y, Mikati MA, Cui J, Grill WM, Yin HH, Yang H.   +7 more
europepmc   +1 more source

Altered GABA_A Receptor Expression in the Primary Somatosensory Cortex of a Mouse Model of Genetic Absence Epilepsy. [PDF]

Int J Mol Sci, 2022
Hassan M, Adotevi NK, Leitch B.
europepmc   +1 more source

Thalamocortical neurons display suppressed burst-firing due to an enhanced Ih current in a genetic model of absence epilepsy [PDF]

, 2014
Stuart M. Cain, John R. Tyson, Karen L. Jones, Terrance P. Snutch   +3 more
openalex   +1 more source

Phenotypic Changes in a Monocyte Cluster with High Interleukin‐1 Beta Expression during Long‐Term Anti‐CD20 Therapy

Annals of Neurology, EarlyView.
Graphical abstract illustrating the study design, experimental workflow, and key findings from single‐cell profiling of peripheral mononuclear cells in multiple sclerosis patients undergoing anti‐CD20 therapy, revealing disease‐ and treatment‐associated immune signatures.
Mie Waede, Christina Kingo, Karina Damsbo, Maiken Uhrbrand Joergensen, Mhaned Oubounyt, Morten Gjerstorff, Mads Thomassen, Jan Baumbach, Jesper B. Moeller, Maria L. Elkjaer, Zsolt Illes   +10 more
wiley   +1 more source

Neuronal rhythmicity and cortical arousal in a mouse model of absence epilepsy. [PDF]

Exp Neurol
Khan W, Chopra S, Zheng X, Liu S, Paszkowski P, Valcarce-Aspegren M, Sieu LA, Mcgill S, Mccafferty C, Blumenfeld H.   +9 more
europepmc   +1 more source

EEG Oscillatory Networks in Peri-Ictal Period of Absence Epilepsy. [PDF]

Front Neurol, 2022
Li Z, Huang J, Wei W, Jiang S, Liu H, Luo H, Ruan J.   +6 more
europepmc   +1 more source

Long‐term seizure remission in childhood absence epilepsy: Might initial treatment matter? [PDF]

, 2014
Anne T. Berg, Susan R. Levy, Francine M. Testa, Hal Blumenfeld   +3 more
openalex   +1 more source

Experimental Treatment Options in Absence Epilepsy.

Current pharmaceutical design, 2017
G. Luijtelaar, M. Zobeiri, A. Lüttjohann, A. Depaulis   +3 more
semanticscholar   +1 more source

Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot–Marie–Tooth Disease

Annals of Neurology, EarlyView.
Objective Charcot–Marie–Tooth (CMT) disease is a heterogeneous group of genetic neuropathies, with >90 genes identified. Several aminoacyl‐tRNA synthetases have been linked to CMT. DARS2, encoding the mitochondrial aspartyl‐tRNA synthetase, has been typically associated with leukoencephalopathy with brainstem and spinal cord involvement and lactate ...
Berta Estévez‐Arias, Siiri Sarv, Nathalie Bonello‐Palot, Laura Carrera‐García, Carlos Ortez, Jesica Expósito‐Escudero, Delia Yubero, Jordi Muchart, Emilien Delmont, Eve Õiglane‐Shlik, Teele Meren, Sanna Puusepp, Ülle Murumets, Gajja S. Salomons, Bjarne Udd, Liis Väli, Lara Cantarero, Carsten G. Bönnemann, Andrés Nascimento, Santiago Ramón‐Maiques, Katrin Õunap, Janet Hoenicka, Daniel Natera‐de Benito, Francesc Palau   +23 more
wiley   +1 more source

Attentional Deficits and Absence Epilepsy: A Tale of 2 Interneuronopathies. [PDF]

Epilepsy Curr
Knowles J.
europepmc   +1 more source