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Brain : a Journal of Neurology
|
September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Dalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Cell Chemical Biology
|
August 9, 2023
Discovery of a highly potent, selective, orally bioavailable inhibitor of KAT6A/B histone acetyltransferases with efficacy against KAT6A-high ER+ breast cancer
Shikhar Sharma, Chi-Yeh Chung, Sean Uryu, et al.
Brain : a Journal of Neurology
|
August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study
Sean 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 Epilepsy
Judy 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 epilepsy
Bo-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 LIFESPAN
Judy 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 study
Christopher 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 epilepsies
Andre 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 subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Science (New York, N.Y.)
|
March 21, 2020
The genetic architecture of the human cerebral cortex
Katrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.
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Showing results (411-420 of 420) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 420 results.
Brain : a Journal of Neurology
|
September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Dalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Cell Chemical Biology
|
August 9, 2023
Discovery of a highly potent, selective, orally bioavailable inhibitor of KAT6A/B histone acetyltransferases with efficacy against KAT6A-high ER+ breast cancer
Shikhar Sharma, Chi-Yeh Chung, Sean Uryu, et al.
Brain : a Journal of Neurology
|
August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study
Sean 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 Epilepsy
Judy 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 epilepsy
Bo-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 LIFESPAN
Judy 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 study
Christopher 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 epilepsies
Andre 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 subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Science (New York, N.Y.)
|
March 21, 2020
The genetic architecture of the human cerebral cortex
Katrina L Grasby, Neda Jahanshad, Jodie N Painter, et al.
Page
of 42