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Peter Galer

Showing results (1-10 of 8) with videos related to

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Journal of Child and Adolescent Psychopharmacology|August 2, 2019
The Effect of Vitamin D Supplementation on Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis of Randomized Controlled TrialsJing Gan, Peter Galer, Dan Ma, et al.
Epilepsia|November 20, 2023
Artificial intelligence in epilepsy phenotypingAndrew Knight, Tilo Gschwind, Peter Galer, et al.
Medicine|August 9, 2019
Mapping the knowledge structure and trends of epilepsy genetics over the past decade: A co-word analysis based on medical subject headings termsJing Gan, Qianyun Cai, Peter Galer, et al.
Frontiers in Neurology|April 20, 2023
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticusDanielle deCampo, Julie Xian, Alexis Karlin, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individualsJan Magielski, Sarah M Ruggiero, Julie Xian, et al.
Communications Biology|September 18, 2023
Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneuronsChad R Camp, Anna Vlachos, Chiara Klöckner, 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 EncephalopathyIngo Helbig, Tania Lopez-Hernandez, Oded Shor, et al.
Brain : a Journal of Neurology|February 22, 2022
Assessing the landscape of STXBP1-related disorders in 534 individualsJulie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Child and Adolescent Psychopharmacology|August 2, 2019
The Effect of Vitamin D Supplementation on Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis of Randomized Controlled TrialsJing Gan, Peter Galer, Dan Ma, et al.
Epilepsia|November 20, 2023
Artificial intelligence in epilepsy phenotypingAndrew Knight, Tilo Gschwind, Peter Galer, et al.
Medicine|August 9, 2019
Mapping the knowledge structure and trends of epilepsy genetics over the past decade: A co-word analysis based on medical subject headings termsJing Gan, Qianyun Cai, Peter Galer, et al.
Frontiers in Neurology|April 20, 2023
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticusDanielle deCampo, Julie Xian, Alexis Karlin, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individualsJan Magielski, Sarah M Ruggiero, Julie Xian, et al.
Communications Biology|September 18, 2023
Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneuronsChad R Camp, Anna Vlachos, Chiara Klöckner, 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 EncephalopathyIngo Helbig, Tania Lopez-Hernandez, Oded Shor, et al.
Brain : a Journal of Neurology|February 22, 2022
Assessing the landscape of STXBP1-related disorders in 534 individualsJulie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, et al.
Pageof 1