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Showing results (181-190 of 353) with videos related to

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JAMA Neurology|October 24, 2022
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy: A Systematic Review and Meta-analysisSiddharth Srivastava, Sara A Lewis, Julie S Cohen, et al.
Cold Spring Harbor Molecular Case Studies|February 3, 2019
Mutations in <i>NRXN1</i> and <i>NRXN2</i> in a patient with early-onset epileptic encephalopathy and respiratory depressionAnne M Rochtus, Sara Trowbridge, Richard D Goldstein, et al.
Epilepsy Currents|January 23, 2020
Epilepsy Benchmarks Area III: Improved Treatment Options for Controlling Seizures and Epilepsy-Related Conditions Without Side EffectsStephen F Traynelis, Dennis Dlugos, David Henshall, et al.
Annals of Neurology|March 27, 2012
Altered inhibition in tuberous sclerosis and type IIb cortical dysplasiaDelia M Talos, Hongyu Sun, Bela Kosaras, et al.
Journal of Child Neurology|January 7, 2017
A Model Program for Translational Medicine in Epilepsy GeneticsLacey A Smith, Jeremy F P Ullmann, Heather E Olson, et al.
Annals of Clinical and Translational Neurology|January 3, 2024
Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disordersAlexandra Santana Almansa, Dustin L Gable, Zoë Frazier, et al.
Acta Virologica|June 8, 2001
Predominance of antibodies to hepatitis C virus envelope proteins in various disease statuses of hepatitis CC D PodurI, A Khanna, S J Khundmiri, et al.
Epilepsia|December 11, 2021
Genetic testing for the epilepsies: A systematic reviewBeth R Sheidley, Jennifer Malinowski, Amanda L Bergner, et al.
Journal of Medicinal Chemistry|January 9, 2004
Discovery of a bulky 2-tert-butyl group containing primaquine analogue that exhibits potent blood-schizontocidal antimalarial activities and complete elimination of methemoglobin toxicityMeenakshi Jain, Suryanarayana Vangapandu, Sandeep Sachdeva, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
Pageof 36

Showing results (181-190 of 353) with videos related to

Sort By:
Pageof 36
JAMA Neurology|October 24, 2022
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy: A Systematic Review and Meta-analysisSiddharth Srivastava, Sara A Lewis, Julie S Cohen, et al.
Cold Spring Harbor Molecular Case Studies|February 3, 2019
Mutations in <i>NRXN1</i> and <i>NRXN2</i> in a patient with early-onset epileptic encephalopathy and respiratory depressionAnne M Rochtus, Sara Trowbridge, Richard D Goldstein, et al.
Epilepsy Currents|January 23, 2020
Epilepsy Benchmarks Area III: Improved Treatment Options for Controlling Seizures and Epilepsy-Related Conditions Without Side EffectsStephen F Traynelis, Dennis Dlugos, David Henshall, et al.
Annals of Neurology|March 27, 2012
Altered inhibition in tuberous sclerosis and type IIb cortical dysplasiaDelia M Talos, Hongyu Sun, Bela Kosaras, et al.
Journal of Child Neurology|January 7, 2017
A Model Program for Translational Medicine in Epilepsy GeneticsLacey A Smith, Jeremy F P Ullmann, Heather E Olson, et al.
Annals of Clinical and Translational Neurology|January 3, 2024
Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disordersAlexandra Santana Almansa, Dustin L Gable, Zoë Frazier, et al.
Acta Virologica|June 8, 2001
Predominance of antibodies to hepatitis C virus envelope proteins in various disease statuses of hepatitis CC D PodurI, A Khanna, S J Khundmiri, et al.
Epilepsia|December 11, 2021
Genetic testing for the epilepsies: A systematic reviewBeth R Sheidley, Jennifer Malinowski, Amanda L Bergner, et al.
Journal of Medicinal Chemistry|January 9, 2004
Discovery of a bulky 2-tert-butyl group containing primaquine analogue that exhibits potent blood-schizontocidal antimalarial activities and complete elimination of methemoglobin toxicityMeenakshi Jain, Suryanarayana Vangapandu, Sandeep Sachdeva, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
Pageof 36