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Epilepsia
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May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
Bronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.
Brain : a Journal of Neurology
|
March 10, 2007
The spectrum of SCN1A-related infantile epileptic encephalopathies
Louise A Harkin, Jacinta M McMahon, Xenia Iona, et al.
Brain : a Journal of Neurology
|
June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)
Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
Epilepsia
|
February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history study
Ingrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.
American Journal of Human Genetics
|
January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Epilepsia Open
|
September 11, 2020
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
Joerg Klepper, Cigdem Akman, Marisa Armeno, et al.
Neurology
|
July 22, 2020
Neuronal antibody prevalence in children with seizures under 3 years: A prospective national cohort
Joseph D Symonds, Teresa C Moloney, Bethan Lang, et al.
Brain : a Journal of Neurology
|
July 15, 2019
Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort
Joseph D Symonds, Sameer M Zuberi, Kirsty Stewart, et al.
Annals of Neurology
|
August 3, 2024
Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS)
Sindhu Viswanathan, Karen L Oliver, Brigid M Regan, et al.
Epilepsia
|
February 25, 2020
Biological concepts in human sodium channel epilepsies and their relevance in clinical practice
Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 123) with videos related to
Sort By:
Page
of 13
Epilepsia
|
May 19, 2015
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
Bronwyn E Grinton, Sarah E Heron, James T Pelekanos, et al.
Brain : a Journal of Neurology
|
March 10, 2007
The spectrum of SCN1A-related infantile epileptic encephalopathies
Louise A Harkin, Jacinta M McMahon, Xenia Iona, et al.
Brain : a Journal of Neurology
|
June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)
Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
Epilepsia
|
February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history study
Ingrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.
American Journal of Human Genetics
|
January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Epilepsia Open
|
September 11, 2020
Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group
Joerg Klepper, Cigdem Akman, Marisa Armeno, et al.
Neurology
|
July 22, 2020
Neuronal antibody prevalence in children with seizures under 3 years: A prospective national cohort
Joseph D Symonds, Teresa C Moloney, Bethan Lang, et al.
Brain : a Journal of Neurology
|
July 15, 2019
Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort
Joseph D Symonds, Sameer M Zuberi, Kirsty Stewart, et al.
Annals of Neurology
|
August 3, 2024
Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS)
Sindhu Viswanathan, Karen L Oliver, Brigid M Regan, et al.
Epilepsia
|
February 25, 2020
Biological concepts in human sodium channel epilepsies and their relevance in clinical practice
Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, et al.
Page
of 13