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Showing results (261-270 of 353) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 20, 2026
DNM1-related disorder is characterized by recurrent variants and phenotypic homogeneityAlicia G Harrison, Shiva Ganesan, Hongbo M Xie, et al.
Brain Communications|April 3, 2025
Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variantsAlissa M D'Gama, Harold Westley Phillips, Yilan Wang, et al.
Annals of Neurology|October 17, 2019
The Genetic Landscape of Epilepsy of Infancy with Migrating Focal SeizuresRosemary Burgess, Shuyu Wang, Amy McTague, et al.
Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variantsAlissa M D'Gama, H Westley Phillips, Yilan Wang, et al.
Molecular Genetics and Metabolism|March 24, 2026
A patient with a rare metabolic disease and myo-inositol administration leading to a new treatment for epilepsyGerard T Berry, E Naomi Vos, Didem Demirbas, et al.
Nature|July 6, 2018
Single-cell analysis of early progenitor cells that build coronary arteriesTianying Su, Geoff Stanley, Rahul Sinha, et al.
Neuron|April 17, 2012
Somatic activation of AKT3 causes hemispheric developmental brain malformationsAnnapurna Poduri, Gilad D Evrony, Xuyu Cai, et al.
NPJ Genomic Medicine|July 14, 2020
Children's rare disease cohorts: an integrative research and clinical genomics initiativeShira Rockowitz, Nicholas LeCompte, Mary Carmack, et al.
Annals of Neurology|January 31, 2017
Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppressionHeather E Olson, McKenna Kelly, Christopher M LaCoursiere, et al.
Human Mutation|August 30, 2008
Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle EastM Chiara Manzini, Danielle Gleason, Bernard S Chang, et al.
Pageof 36

Showing results (261-270 of 353) with videos related to

Sort By:
Pageof 36
Medrxiv : the Preprint Server for Health Sciences|April 20, 2026
DNM1-related disorder is characterized by recurrent variants and phenotypic homogeneityAlicia G Harrison, Shiva Ganesan, Hongbo M Xie, et al.
Brain Communications|April 3, 2025
Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variantsAlissa M D'Gama, Harold Westley Phillips, Yilan Wang, et al.
Annals of Neurology|October 17, 2019
The Genetic Landscape of Epilepsy of Infancy with Migrating Focal SeizuresRosemary Burgess, Shuyu Wang, Amy McTague, et al.
Medrxiv : the Preprint Server for Health Sciences|August 7, 2024
Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variantsAlissa M D'Gama, H Westley Phillips, Yilan Wang, et al.
Molecular Genetics and Metabolism|March 24, 2026
A patient with a rare metabolic disease and myo-inositol administration leading to a new treatment for epilepsyGerard T Berry, E Naomi Vos, Didem Demirbas, et al.
Nature|July 6, 2018
Single-cell analysis of early progenitor cells that build coronary arteriesTianying Su, Geoff Stanley, Rahul Sinha, et al.
Neuron|April 17, 2012
Somatic activation of AKT3 causes hemispheric developmental brain malformationsAnnapurna Poduri, Gilad D Evrony, Xuyu Cai, et al.
NPJ Genomic Medicine|July 14, 2020
Children's rare disease cohorts: an integrative research and clinical genomics initiativeShira Rockowitz, Nicholas LeCompte, Mary Carmack, et al.
Annals of Neurology|January 31, 2017
Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppressionHeather E Olson, McKenna Kelly, Christopher M LaCoursiere, et al.
Human Mutation|August 30, 2008
Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle EastM Chiara Manzini, Danielle Gleason, Bernard S Chang, et al.
Pageof 36