Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
Science Advances|November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA studySara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, et al.
Nature Communications|July 27, 2022
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expressionSara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Brain : a Journal of Neurology|September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Brain : a Journal of Neurology|August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy studySean N Hatton, Khoa H Huynh, Leonardo Bonilha, et al.
Neurology|August 22, 2025
Changes in Gray Matter Morphology and White Matter Microstructure Across the Adult Lifespan in People With Temporal Lobe EpilepsyJudy Chen, Alexander Ngo, Raul Rodriguez-Cruces, et al.
Brain : a Journal of Neurology|March 25, 2022
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsyBo-Yong Park, Sara Larivière, Raul Rodríguez-Cruces, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
A WORLDWIDE ENIGMA STUDY ON EPILEPSY-RELATED GRAY AND WHITE MATTER COMPROMISE ACROSS THE ADULT LIFESPANJudy Chen, Alexander Ngo, Raúl Rodríguez-Cruces, et al.
Brain : a Journal of Neurology|January 25, 2018
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA studyChristopher D Whelan, Andre Altmann, Juan A Botía, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Pageof 12