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Brain Communications
|
January 17, 2024
Long-term predictors of developmental outcome and disease burden in <i>SCN1A</i>-positive Dravet syndrome
Tony Feng, Phoebe Makiello, Benjamin Dunwoody, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 16, 2025
Trauma, coping, and adjustment when parenting a child with Dravet syndrome
Anthony Mercier, Liam Dorris, Andreas Brunklaus, et al.
Epilepsia
|
June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk
Kenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 7, 2024
Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study
Erin Freeman-Jones, Galia Wilson, Claire Eldred, et al.
Brain : a Journal of Neurology
|
January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapy
Andreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Epilepsy & Behavior Reports
|
November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited setting
Priyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
Human Mutation
|
November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterization
Andreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.
Neurology. Genetics
|
April 27, 2026
Elicited Repetitive Daily Blindness Associated With Gain-of-Function <i>SCN1A</i> Variants and Responsiveness to Sodium Channel Blockers
Sandrine Cestèle, Alexander James Harper, Sebastian Marra, et al.
BMJ Open
|
September 16, 2022
Rates, causes and predictors of all-cause and avoidable mortality in 163 686 children and young people with and without intellectual disabilities: a record linkage national cohort study
Laura Anne Hughes-McCormack, Ewelina Rydzewska, Sally-Ann Cooper, et al.
Epilepsia
|
February 11, 2025
SCN1A pathogenic variants do not have a distinctive blood-derived DNA methylation signature
Christy W LaFlamme, Karim Karimi, Cassandra Rastin, et al.
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Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Brain Communications
|
January 17, 2024
Long-term predictors of developmental outcome and disease burden in <i>SCN1A</i>-positive Dravet syndrome
Tony Feng, Phoebe Makiello, Benjamin Dunwoody, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 16, 2025
Trauma, coping, and adjustment when parenting a child with Dravet syndrome
Anthony Mercier, Liam Dorris, Andreas Brunklaus, et al.
Epilepsia
|
June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk
Kenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 7, 2024
Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study
Erin Freeman-Jones, Galia Wilson, Claire Eldred, et al.
Brain : a Journal of Neurology
|
January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapy
Andreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Epilepsy & Behavior Reports
|
November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited setting
Priyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
Human Mutation
|
November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterization
Andreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.
Neurology. Genetics
|
April 27, 2026
Elicited Repetitive Daily Blindness Associated With Gain-of-Function <i>SCN1A</i> Variants and Responsiveness to Sodium Channel Blockers
Sandrine Cestèle, Alexander James Harper, Sebastian Marra, et al.
BMJ Open
|
September 16, 2022
Rates, causes and predictors of all-cause and avoidable mortality in 163 686 children and young people with and without intellectual disabilities: a record linkage national cohort study
Laura Anne Hughes-McCormack, Ewelina Rydzewska, Sally-Ann Cooper, et al.
Epilepsia
|
February 11, 2025
SCN1A pathogenic variants do not have a distinctive blood-derived DNA methylation signature
Christy W LaFlamme, Karim Karimi, Cassandra Rastin, et al.
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of 4