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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 Vision
Lauren 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 HIV
Marilyn 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 Perspective
Thomas 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 disorder
Jonathan 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 Trial
Kelly 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 Cohort
Zachary M Grinspan, Kelly G Knupp, Anup D Patel, et al.
Epilepsia
|
June 18, 2025
Comparative effectiveness of second-line treatments for epileptic spasms
Kristen 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 Defects
Jinglan 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 guidance
Amélie 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 encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
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Search research articles
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Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 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 Vision
Lauren 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 HIV
Marilyn 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 Perspective
Thomas 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 disorder
Jonathan 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 Trial
Kelly 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 Cohort
Zachary M Grinspan, Kelly G Knupp, Anup D Patel, et al.
Epilepsia
|
June 18, 2025
Comparative effectiveness of second-line treatments for epileptic spasms
Kristen 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 Defects
Jinglan 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 guidance
Amélie 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 encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Page
of 5