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Louis T Dang

Showing results (11-20 of 34) with videos related to

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Journal of Visualized Experiments : Jove|October 14, 2024
A Multi-Electrode Array Platform for Modeling Epilepsy Using Human Pluripotent Stem Cell-Derived Brain AssembloidsTong Pan, Daniel C Jaklic, Shivanshi Vaid, et al.
Pediatric Neurology|April 19, 2020
Dramatic Improvement in Seizures With Phenytoin Treatment in an Individual With Refractory Epilepsy and a SCN1B VariantLouis T Dang, Shane C Quinonez, Bridget R Becka, et al.
The Journal of Pediatrics|November 24, 2020
Seizure Rescue Medications for Out-Of-Hospital Use in ChildrenErin M Fedak Romanowski, Nancy A McNamara, Erin E Neil, et al.
Neurology. Genetics|July 15, 2025
The Association Between Sleep Phenotypes and Epilepsy GenesJonathan Read Gaillard, Gita Gupta, Heather C Mefford, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
<i>RAI1</i> safeguards fidelity and tempo of human neurodevelopmental gene expressionBo Zhou, Satabdi Mohanty, Paris Riggle, et al.
Pediatrics|August 13, 2014
Subdural hemorrhages associated with antithrombotic therapy in infants with cerebral atrophyLouis T Dang, Jordan A Shavit, Rani K Singh, et al.
Stem Cell Reports|August 8, 2017
Rapid Generation of Human Genetic Loss-of-Function iPSC Lines by Simultaneous Reprogramming and Gene EditingAndrew M Tidball, Louis T Dang, Trevor W Glenn, et al.
BMC Bioinformatics|February 15, 2022
MonaGO: a novel gene ontology enrichment analysis visualisation systemZiyin Xin, Yujun Cai, Louis T Dang, et al.
Developmental Neurobiology|February 23, 2021
STRADA-mutant human cortical organoids model megalencephaly and exhibit delayed neuronal differentiationLouis T Dang, Shivanshi Vaid, Grace Lin, et al.
Children (Basel, Switzerland)|October 27, 2022
SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic EncephalopathyZahra Zhu, Elizabeth Bolt, Kyra Newmaster, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Journal of Visualized Experiments : Jove|October 14, 2024
A Multi-Electrode Array Platform for Modeling Epilepsy Using Human Pluripotent Stem Cell-Derived Brain AssembloidsTong Pan, Daniel C Jaklic, Shivanshi Vaid, et al.
Pediatric Neurology|April 19, 2020
Dramatic Improvement in Seizures With Phenytoin Treatment in an Individual With Refractory Epilepsy and a SCN1B VariantLouis T Dang, Shane C Quinonez, Bridget R Becka, et al.
The Journal of Pediatrics|November 24, 2020
Seizure Rescue Medications for Out-Of-Hospital Use in ChildrenErin M Fedak Romanowski, Nancy A McNamara, Erin E Neil, et al.
Neurology. Genetics|July 15, 2025
The Association Between Sleep Phenotypes and Epilepsy GenesJonathan Read Gaillard, Gita Gupta, Heather C Mefford, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
<i>RAI1</i> safeguards fidelity and tempo of human neurodevelopmental gene expressionBo Zhou, Satabdi Mohanty, Paris Riggle, et al.
Pediatrics|August 13, 2014
Subdural hemorrhages associated with antithrombotic therapy in infants with cerebral atrophyLouis T Dang, Jordan A Shavit, Rani K Singh, et al.
Stem Cell Reports|August 8, 2017
Rapid Generation of Human Genetic Loss-of-Function iPSC Lines by Simultaneous Reprogramming and Gene EditingAndrew M Tidball, Louis T Dang, Trevor W Glenn, et al.
BMC Bioinformatics|February 15, 2022
MonaGO: a novel gene ontology enrichment analysis visualisation systemZiyin Xin, Yujun Cai, Louis T Dang, et al.
Developmental Neurobiology|February 23, 2021
STRADA-mutant human cortical organoids model megalencephaly and exhibit delayed neuronal differentiationLouis T Dang, Shivanshi Vaid, Grace Lin, et al.
Children (Basel, Switzerland)|October 27, 2022
SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic EncephalopathyZahra Zhu, Elizabeth Bolt, Kyra Newmaster, et al.
Pageof 4