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Journal of Autism and Developmental Disorders
|
June 24, 2018
Enhanced Sensitivity to Angry Voices in People with Features of the Broader Autism Phenotype
Valerie M Z Yap, Neil M McLachlan, Ingrid E Scheffer, et al.
Epilepsy Research
|
January 25, 2011
Electroclinical features of absence seizures in sleep
Lynette G Sadleir, Kevin Farrell, Sherry Smith, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 2, 2021
Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants
Abdulla Alawadhi, Angela T Morgan, Bettina E Mucha, et al.
The Lancet. Neurology
|
November 25, 2015
The genetic landscape of the epileptic encephalopathies of infancy and childhood
Amy McTague, Katherine B Howell, J Helen Cross, et al.
Epilepsia
|
May 25, 2007
Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?
Isabella Taylor, Bree Hodgson, Ingrid E Scheffer, et al.
Developmental Medicine and Child Neurology
|
February 24, 2018
Stiripentol efficacy and safety in Dravet syndrome: a 12-year observational study
Kenneth A Myers, Paul Lightfoot, Shekhar G Patil, et al.
Developmental Medicine and Child Neurology
|
January 26, 2019
Speech and language in bilateral perisylvian polymicrogyria: a systematic review
Ruth O Braden, Richard J Leventer, Anna Jansen, et al.
Epilepsia
|
February 8, 2023
Differential diagnosis of familial adult myoclonic epilepsy
Betul Baykan, Silvana Franceschetti, Laura Canafoglia, et al.
Epilepsia
|
December 5, 2012
Family studies of individuals with eyelid myoclonia with absences
Lynette G Sadleir, Danya Vears, Brigid Regan, et al.
Epilepsy Research
|
April 17, 2007
Association studies and functional validation or functional validation alone?
Sarah E Heron, Louisa Sanchez, Ingrid E Scheffer, et al.
Page
of 59
Search research articles
Search
Showing results (91-100 of 585) with videos related to
Sort By:
Page
of 59
Journal of Autism and Developmental Disorders
|
June 24, 2018
Enhanced Sensitivity to Angry Voices in People with Features of the Broader Autism Phenotype
Valerie M Z Yap, Neil M McLachlan, Ingrid E Scheffer, et al.
Epilepsy Research
|
January 25, 2011
Electroclinical features of absence seizures in sleep
Lynette G Sadleir, Kevin Farrell, Sherry Smith, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 2, 2021
Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants
Abdulla Alawadhi, Angela T Morgan, Bettina E Mucha, et al.
The Lancet. Neurology
|
November 25, 2015
The genetic landscape of the epileptic encephalopathies of infancy and childhood
Amy McTague, Katherine B Howell, J Helen Cross, et al.
Epilepsia
|
May 25, 2007
Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?
Isabella Taylor, Bree Hodgson, Ingrid E Scheffer, et al.
Developmental Medicine and Child Neurology
|
February 24, 2018
Stiripentol efficacy and safety in Dravet syndrome: a 12-year observational study
Kenneth A Myers, Paul Lightfoot, Shekhar G Patil, et al.
Developmental Medicine and Child Neurology
|
January 26, 2019
Speech and language in bilateral perisylvian polymicrogyria: a systematic review
Ruth O Braden, Richard J Leventer, Anna Jansen, et al.
Epilepsia
|
February 8, 2023
Differential diagnosis of familial adult myoclonic epilepsy
Betul Baykan, Silvana Franceschetti, Laura Canafoglia, et al.
Epilepsia
|
December 5, 2012
Family studies of individuals with eyelid myoclonia with absences
Lynette G Sadleir, Danya Vears, Brigid Regan, et al.
Epilepsy Research
|
April 17, 2007
Association studies and functional validation or functional validation alone?
Sarah E Heron, Louisa Sanchez, Ingrid E Scheffer, et al.
Page
of 59