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Epilepsia
|
March 21, 2002
Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters
Rita Singh, R J McKinlay Gardner, Kathryn M Crossland, et al.
Epilepsia
|
February 27, 2025
Operational definition of developmental and epileptic encephalopathies to underpin the design of therapeutic trials
Ingrid E Scheffer, Jacqueline French, Kette D Valente, et al.
Neurology. Genetics
|
April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery
Karen L Oliver, Vesna Lukic, Saskia Freytag, et al.
Pharmacological Reviews
|
December 22, 2017
Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, et al.
Epilepsia
|
January 9, 2013
Siblings with refractory occipital epilepsy showing localized network activity on EEG-fMRI
Patrick W Carney, A Simon Harvey, Samuel F Berkovic, et al.
Human Molecular Genetics
|
October 26, 2005
Susceptibility genes for complex epilepsy
John C Mulley, Ingrid E Scheffer, Louise A Harkin, et al.
Epilepsia
|
February 27, 2009
EEG features of absence seizures in idiopathic generalized epilepsy: impact of syndrome, age, and state
Lynette Grant Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Epilepsy & Behavior : E&B
|
August 29, 2020
Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome
Amy Brown, Marta Arpone, Amy L Schneider, et al.
Epilepsia Open
|
July 4, 2024
Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox-Gastaut syndrome in clinical practice
Elaine C Wirrell, Lieven Lagae, Ingrid E Scheffer, et al.
Annals of Clinical and Translational Neurology
|
April 7, 2017
Is a microRNA-328 binding site in <i>PAX6</i> associated with Rolandic epilepsy?
Amelia McGlade, Kenneth A Myers, Samuel F Berkovic, et al.
Page
of 59
Search research articles
Search
Showing results (111-120 of 586) with videos related to
Sort By:
Page
of 59
Epilepsia
|
March 21, 2002
Chromosomal abnormalities and epilepsy: a review for clinicians and gene hunters
Rita Singh, R J McKinlay Gardner, Kathryn M Crossland, et al.
Epilepsia
|
February 27, 2025
Operational definition of developmental and epileptic encephalopathies to underpin the design of therapeutic trials
Ingrid E Scheffer, Jacqueline French, Kette D Valente, et al.
Neurology. Genetics
|
April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery
Karen L Oliver, Vesna Lukic, Saskia Freytag, et al.
Pharmacological Reviews
|
December 22, 2017
Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, et al.
Epilepsia
|
January 9, 2013
Siblings with refractory occipital epilepsy showing localized network activity on EEG-fMRI
Patrick W Carney, A Simon Harvey, Samuel F Berkovic, et al.
Human Molecular Genetics
|
October 26, 2005
Susceptibility genes for complex epilepsy
John C Mulley, Ingrid E Scheffer, Louise A Harkin, et al.
Epilepsia
|
February 27, 2009
EEG features of absence seizures in idiopathic generalized epilepsy: impact of syndrome, age, and state
Lynette Grant Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Epilepsy & Behavior : E&B
|
August 29, 2020
Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome
Amy Brown, Marta Arpone, Amy L Schneider, et al.
Epilepsia Open
|
July 4, 2024
Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox-Gastaut syndrome in clinical practice
Elaine C Wirrell, Lieven Lagae, Ingrid E Scheffer, et al.
Annals of Clinical and Translational Neurology
|
April 7, 2017
Is a microRNA-328 binding site in <i>PAX6</i> associated with Rolandic epilepsy?
Amelia McGlade, Kenneth A Myers, Samuel F Berkovic, et al.
Page
of 59