Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Lowenstein

Showing results (241-250 of 255) with videos related to

Pageof 26
Sort By:
Epilepsia|March 24, 2011
Common data elements in epilepsy research: development and implementation of the NINDS epilepsy CDE projectDavid W Loring, Daniel H Lowenstein, Nicholas M Barbaro, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
Further delineation of the clinical spectrum of de novo TRIM8 truncating mutationsMirna Assoum, Matthew A Lines, Orly Elpeleg, et al.
Journal of Neuroinflammation|May 9, 2026
Mechanistically informed circulating biomarkers are associated with acquired epilepsy after neonatal brain injuryAdam L Numis, Renée A Shellhaas, Janet S Soul, et al.
Epilepsy Currents|June 12, 2025
American Epilepsy Society/International League Against Epilepsy-North America Joint Task Force for Epilepsy Health Care Disparities in the United StatesJaideep Kapur, Dave Clarke, Mill Etienne, et al.
Neurology|May 25, 2021
Early Neurologic Recovery, Practice Pattern Variation, and the Risk of Endotracheal Intubation Following Established Status EpilepticusEric S Rosenthal, Jordan J Elm, James Ingles, et al.
Epilepsia|December 17, 2017
Commonalities in epileptogenic processes from different acute brain insults: Do they translate?Pavel Klein, Raymond Dingledine, Eleonora Aronica, et al.
Human Genetics|April 11, 2017
Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disabilityNuria C Bramswig, Hermann-Josef Lüdecke, Fadi F Hamdan, et al.
Epilepsia|March 16, 2024
Clinical and molecular characterization of patients with YWHAG-related epilepsyValentina Cetica, Tiziana Pisano, Gaetan Lesca, et al.
American Journal of Human Genetics|September 26, 2017
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with SeizuresCandace T Myers, Nicholas Stong, Emily I Mountier, et al.
Cell|July 28, 2018
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric DisordersA Jeremy Willsey, Montana T Morris, Sheng Wang, et al.
Pageof 26

Showing results (241-250 of 255) with videos related to

Sort By:
Pageof 26
Epilepsia|March 24, 2011
Common data elements in epilepsy research: development and implementation of the NINDS epilepsy CDE projectDavid W Loring, Daniel H Lowenstein, Nicholas M Barbaro, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
Further delineation of the clinical spectrum of de novo TRIM8 truncating mutationsMirna Assoum, Matthew A Lines, Orly Elpeleg, et al.
Journal of Neuroinflammation|May 9, 2026
Mechanistically informed circulating biomarkers are associated with acquired epilepsy after neonatal brain injuryAdam L Numis, Renée A Shellhaas, Janet S Soul, et al.
Epilepsy Currents|June 12, 2025
American Epilepsy Society/International League Against Epilepsy-North America Joint Task Force for Epilepsy Health Care Disparities in the United StatesJaideep Kapur, Dave Clarke, Mill Etienne, et al.
Neurology|May 25, 2021
Early Neurologic Recovery, Practice Pattern Variation, and the Risk of Endotracheal Intubation Following Established Status EpilepticusEric S Rosenthal, Jordan J Elm, James Ingles, et al.
Epilepsia|December 17, 2017
Commonalities in epileptogenic processes from different acute brain insults: Do they translate?Pavel Klein, Raymond Dingledine, Eleonora Aronica, et al.
Human Genetics|April 11, 2017
Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disabilityNuria C Bramswig, Hermann-Josef Lüdecke, Fadi F Hamdan, et al.
Epilepsia|March 16, 2024
Clinical and molecular characterization of patients with YWHAG-related epilepsyValentina Cetica, Tiziana Pisano, Gaetan Lesca, et al.
American Journal of Human Genetics|September 26, 2017
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with SeizuresCandace T Myers, Nicholas Stong, Emily I Mountier, et al.
Cell|July 28, 2018
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric DisordersA Jeremy Willsey, Montana T Morris, Sheng Wang, et al.
Pageof 26