Search research articles
Contact Us
Filters
Showing results (21-30 of 25) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 25 results.
Journal of the Neurological Sciences
|
September 21, 2025
West Nile virus neuroinvasive disease: Clinical characteristics and prognostic factors
Tali Elkanovich, Gal Tsur, Keshet Pardo, et al.
Neurology. Genetics
|
March 25, 2021
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin
Adi Wilf-Yarkoni, Oded Shor, Avi Fellner, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 8, 2026
Paroxysmal Slow Waves Mark Ictal Networks
Florent J M Boyer-Aymé, Hamza Imtiaz, Ofer Prager, et al.
Epilepsia
|
June 20, 2026
Paroxysmal slow waves mark ictal networks
Florent J M Boyer-Aymé, Hamza Imtiaz, Ofer Prager, et al.
American Journal of Human Genetics
|
May 21, 2019
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
Ingo Helbig, Tania Lopez-Hernandez, Oded Shor, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Journal of the Neurological Sciences
|
September 21, 2025
West Nile virus neuroinvasive disease: Clinical characteristics and prognostic factors
Tali Elkanovich, Gal Tsur, Keshet Pardo, et al.
Neurology. Genetics
|
March 25, 2021
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin
Adi Wilf-Yarkoni, Oded Shor, Avi Fellner, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 8, 2026
Paroxysmal Slow Waves Mark Ictal Networks
Florent J M Boyer-Aymé, Hamza Imtiaz, Ofer Prager, et al.
Epilepsia
|
June 20, 2026
Paroxysmal slow waves mark ictal networks
Florent J M Boyer-Aymé, Hamza Imtiaz, Ofer Prager, et al.
American Journal of Human Genetics
|
May 21, 2019
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
Ingo Helbig, Tania Lopez-Hernandez, Oded Shor, et al.
Page
of 3