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Plos One
|
January 9, 2025
Interrogating green social prescribing in South Wales; A multi-stakeholder qualitative exploration
Menna Brown, Katharine Sarah Aylett
Archives of Disease in Childhood
|
January 13, 2021
Work of a paediatric bioethics centre during the COVID-19 pandemic first phase
Joe Brierley, Sarah Aylett, Anne MacNiven, et al.
Clinical Ethics
|
May 23, 2023
North Thames multi-centre service evaluation: Ethical considerations during COVID-19
Namithaa Sunil Kumar, Pippa Sipanoun, Mariana Dittborn, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
July 22, 2021
Neurological presentations and cognitive outcome in Sturge-Weber syndrome
Sebastian Powell, Tangunu Fosi, Jenny Sloneem, et al.
Journal of Autism and Developmental Disorders
|
May 27, 2021
The prevalence and profile of autism in Sturge-Weber syndrome
Jenny Sloneem, Jo Moss, Sebastian Powell, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families
Andreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 15, 2026
Seizure and developmental outcomes following epilepsy surgery for children with Sturge-Weber syndrome
Jonathan Cookson, Hanna Richardson, Martin Tisdall, et al.
Epilepsia
|
September 3, 2020
Diagnostic algorithm for children presenting with epilepsia partialis continua
Snehal Surana, Thomas Rossor, Jane Hassell, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
September 16, 2005
Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reports
Matthew Walker, Helen Cross, Shelagh Smith, 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.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Plos One
|
January 9, 2025
Interrogating green social prescribing in South Wales; A multi-stakeholder qualitative exploration
Menna Brown, Katharine Sarah Aylett
Archives of Disease in Childhood
|
January 13, 2021
Work of a paediatric bioethics centre during the COVID-19 pandemic first phase
Joe Brierley, Sarah Aylett, Anne MacNiven, et al.
Clinical Ethics
|
May 23, 2023
North Thames multi-centre service evaluation: Ethical considerations during COVID-19
Namithaa Sunil Kumar, Pippa Sipanoun, Mariana Dittborn, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
July 22, 2021
Neurological presentations and cognitive outcome in Sturge-Weber syndrome
Sebastian Powell, Tangunu Fosi, Jenny Sloneem, et al.
Journal of Autism and Developmental Disorders
|
May 27, 2021
The prevalence and profile of autism in Sturge-Weber syndrome
Jenny Sloneem, Jo Moss, Sebastian Powell, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families
Andreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 15, 2026
Seizure and developmental outcomes following epilepsy surgery for children with Sturge-Weber syndrome
Jonathan Cookson, Hanna Richardson, Martin Tisdall, et al.
Epilepsia
|
September 3, 2020
Diagnostic algorithm for children presenting with epilepsia partialis continua
Snehal Surana, Thomas Rossor, Jane Hassell, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
September 16, 2005
Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reports
Matthew Walker, Helen Cross, Shelagh Smith, 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.
Page
of 1