Cargando…

Cardiac arrhythmias in Dravet syndrome: an observational multicenter study

OBJECTIVES: We ascertained the prevalence of ictal arrhythmias to explain the high rate of sudden unexpected death in epilepsy (SUDEP) in Dravet syndrome (DS). METHODS: We selected cases with clinical DS, ≥6 years, SCN1A mutation, and ≥1 seizure/week. Home‐based ECG recordings were performed for 20 ...

Descripción completa

Detalles Bibliográficos
Autores principales:	Shmuely, Sharon, Surges, Rainer, Helling, Robert M., Gunning, W. Boudewijn, Brilstra, Eva H., Verhoeven, Judith S., Cross, J. Helen, Sisodiya, Sanjay M., Tan, Hanno L., Sander, Josemir W., Thijs, Roland D.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2020
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187713/ https://www.ncbi.nlm.nih.gov/pubmed/32207228 http://dx.doi.org/10.1002/acn3.51017

Ejemplares similares

Cardiac arrhythmias during or after epileptic seizures
por: van der Lende, Marije, et al.
Publicado: (2016)

Impaired intracortical inhibition demonstrated in vivo in people with Dravet syndrome
por: Stern, William M., et al.
Publicado: (2017)

Case report: Dravet syndrome, feeding difficulties and gastrostomy
por: Clayton, Lisa M., et al.
Publicado: (2022)

Audit of use of stiripentol in adults with Dravet syndrome
por: Balestrini, S., et al.
Publicado: (2016)

The impact of COVID‐19 in Dravet syndrome: A UK survey
por: Balestrini, Simona, et al.
Publicado: (2021)

The impact of SARS-CoV-2 vaccination in Dravet syndrome: A UK survey
por: Clayton, Lisa M., et al.
Publicado: (2021)

Time to onset of cannabidiol treatment effects in Dravet syndrome: Analysis from two randomized controlled trials
por: Madan Cohen, Jennifer, et al.
Publicado: (2021)

Late diagnoses of Dravet syndrome: How many individuals are we missing?
por: Silvennoinen, Katri, et al.
Publicado: (2021)

Tracking cortical excitability dynamics with transcranial magnetic stimulation in focal epilepsy
por: Helling, Robert M., et al.
Publicado: (2022)

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology
por: Catarino, Claudia B., et al.
Publicado: (2011)

Timing of syncope in ictal asystole as a guide when considering pacemaker implantation
por: van Westrhenen, Anouk, et al.
Publicado: (2021)

Dravet syndrome
por: Incorpora, Gemma
Publicado: (2009)

Dose-Ranging Effect of Adjunctive Oral Cannabidiol vs Placebo on Convulsive Seizure Frequency in Dravet Syndrome: A Randomized Clinical Trial
por: Miller, Ian, et al.
Publicado: (2020)

Transcranial magnetic stimulation‐evoked electroencephalography responses as biomarkers for epilepsy: A review of study design and outcomes
por: Gefferie, Silvano R., et al.
Publicado: (2023)

Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition
por: Martins Custodio, Helena, et al.
Publicado: (2023)

Vaccinations and Dravet Syndrome
por: Korff, Christian M.
Publicado: (2015)

Phenotypes of Dravet Syndrome
por: Garcia-Sosa, Rebecca, et al.
Publicado: (2016)

Dravet Syndrome: An Overview
por: Anwar, Arsalan, et al.
Publicado: (2019)

Stiripentol for Dravet syndrome
Publicado: (2020)

Recurrent schizophrenia-like psychosis as first manifestation of epilepsy: a diagnostic challenge in neuropsychiatry
por: Verhoeven, Willem MA, et al.
Publicado: (2010)

Crouch Gait in Dravet Syndrome
por: Black, Laura, et al.
Publicado: (2016)

Anesthetic considerations in Dravet syndrome
por: Macdonald‐Laurs, Emma, et al.
Publicado: (2022)

Open the Window for the Cure of Dravet
por: Gu, Bin
Publicado: (2022)

Two Perspectives on Dravet Syndrome: Viewpoints from the Clinician and the Caregiver
por: Bluvstein, Judith, et al.
Publicado: (2023)

Spontaneously Fluctuating Motor Cortex Excitability in Alternating Hemiplegia of Childhood: A Transcranial Magnetic Stimulation Study
por: Stern, William M., et al.
Publicado: (2016)

Do All Roads Lead to Rome? Genes Causing Dravet Syndrome and Dravet Syndrome-Like Phenotypes
por: Ding, Jiangwei, et al.
Publicado: (2022)

Fatal Status Epilepticus in Dravet Syndrome
por: De Liso, Paola, et al.
Publicado: (2020)

Prevalence of SCN1A-Related Dravet Syndrome among Children Reported with Seizures following Vaccination: A Population-Based Ten-Year Cohort Study
por: Verbeek, Nienke E., et al.
Publicado: (2013)

Recurrence risk of ictal asystole in epilepsy
por: Hampel, Kevin G., et al.
Publicado: (2017)

The Impact of Head-Up Tilt Sleeping on Orthostatic Tolerance: A Scoping Review
por: van der Stam, Amber H., et al.
Publicado: (2023)

Low‐dose fenfluramine significantly reduces seizure frequency in Dravet syndrome: a prospective study of a new cohort of patients
por: Schoonjans, A., et al.
Publicado: (2016)

Incidence of Dravet Syndrome in a US Population
por: Krueger, Jena, et al.
Publicado: (2015)

Dravet Syndrome: A Developmental and Epileptic Encephalopathy
por: Lopez-Santiago, Luis, et al.
Publicado: (2019)

Fenfluramine: New Treatment for Seizures in Dravet Syndrome
por: Pierce, Joanna Garcia, et al.
Publicado: (2020)

Dravet Syndrome—The Polish Family’s Perspective Study
por: Paprocka, Justyna, et al.
Publicado: (2021)

Patient with Dravet syndrome: A case report
por: Yadav, Rukesh, et al.
Publicado: (2022)

International consensus on diagnosis and management of Dravet syndrome
por: Wirrell, Elaine C., et al.
Publicado: (2022)

A registry for Dravet syndrome: The Italian experience
por: Balestrini, Simona, et al.
Publicado: (2023)

The psychosocial impact of caring for children with Dravet Syndrome
por: Salom, Rafael, et al.
Publicado: (2023)

Dravet Syndrome as an Example of Precision Medicine in Epilepsy
por: Sullivan, Joseph, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_qfmujcuc88ivdfo7903nge9els