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Wendy G Mitchell

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Pediatric Neurology|September 16, 2023
An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and VisionLauren M Kerr, Morgan E Ryan, Ming Lim, et al.
The Journal of Infectious Diseases|June 11, 2010
Possible mitochondrial dysfunction and its association with antiretroviral therapy use in children perinatally infected with HIVMarilyn J Crain, Miriam C Chernoff, James M Oleske, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 9, 2022
Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International PerspectiveThomas Rossor, E Ann Yeh, Yasmin Khakoo, et al.
American Journal of Medical Genetics. Part A|January 3, 2024
Safety and tolerability of intravenous immunoglobulin infusion in Down syndrome regression disorderJonathan D Santoro, Saba Jafarpour, Mellad M Khoshnood, et al.
Journal of Child Neurology|January 19, 2022
Comparison of Cosyntropin, Vigabatrin, and Combination Therapy in New-Onset Infantile Spasms in a Prospective Randomized TrialKelly G Knupp, Jason Coryell, Rani K Singh, et al.
Neurology|July 16, 2021
Comparative Effectiveness of Initial Treatment for Infantile Spasms in a Contemporary US CohortZachary M Grinspan, Kelly G Knupp, Anup D Patel, et al.
Epilepsia|June 18, 2025
Comparative effectiveness of second-line treatments for epileptic spasmsKristen Barbour, Shaun A Hussain, Kelly G Knupp, et al.
Plos Genetics|April 28, 2016
A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic DefectsJinglan Zhang, Véronik Lachance, Adam Schaffner, et al.
Human Molecular Genetics|May 23, 2022
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidanceAmélie Cordovado, Martina Schaettin, Médéric Jeanne, et al.
Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Pediatric Neurology|September 16, 2023
An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and VisionLauren M Kerr, Morgan E Ryan, Ming Lim, et al.
The Journal of Infectious Diseases|June 11, 2010
Possible mitochondrial dysfunction and its association with antiretroviral therapy use in children perinatally infected with HIVMarilyn J Crain, Miriam C Chernoff, James M Oleske, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 9, 2022
Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia Syndrome in Children: An International PerspectiveThomas Rossor, E Ann Yeh, Yasmin Khakoo, et al.
American Journal of Medical Genetics. Part A|January 3, 2024
Safety and tolerability of intravenous immunoglobulin infusion in Down syndrome regression disorderJonathan D Santoro, Saba Jafarpour, Mellad M Khoshnood, et al.
Journal of Child Neurology|January 19, 2022
Comparison of Cosyntropin, Vigabatrin, and Combination Therapy in New-Onset Infantile Spasms in a Prospective Randomized TrialKelly G Knupp, Jason Coryell, Rani K Singh, et al.
Neurology|July 16, 2021
Comparative Effectiveness of Initial Treatment for Infantile Spasms in a Contemporary US CohortZachary M Grinspan, Kelly G Knupp, Anup D Patel, et al.
Epilepsia|June 18, 2025
Comparative effectiveness of second-line treatments for epileptic spasmsKristen Barbour, Shaun A Hussain, Kelly G Knupp, et al.
Plos Genetics|April 28, 2016
A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic DefectsJinglan Zhang, Véronik Lachance, Adam Schaffner, et al.
Human Molecular Genetics|May 23, 2022
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidanceAmélie Cordovado, Martina Schaettin, Médéric Jeanne, et al.
Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Pageof 5