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M Walley

Showing results (151-160 of 157) with videos related to

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Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
European Journal of Human Genetics : EJHG|December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative geneEleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Brain : a Journal of Neurology|April 20, 2022
Somatic variants in diverse genes leads to a spectrum of focal cortical malformationsDulcie Lai, Meethila Gade, Edward Yang, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyErin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, et al.
The New England Journal of Medicine|October 11, 2018
Effect of Genetic Diagnosis on Patients with Previously Undiagnosed DiseaseKimberly Splinter, David R Adams, Carlos A Bacino, et al.
Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
European Journal of Human Genetics : EJHG|December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative geneEleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Brain : a Journal of Neurology|April 20, 2022
Somatic variants in diverse genes leads to a spectrum of focal cortical malformationsDulcie Lai, Meethila Gade, Edward Yang, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyErin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, et al.
The New England Journal of Medicine|October 11, 2018
Effect of Genetic Diagnosis on Patients with Previously Undiagnosed DiseaseKimberly Splinter, David R Adams, Carlos A Bacino, et al.
Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Pageof 16