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Physiological Measurement
|
May 21, 2024
Multimodal wearable EEG, EMG and accelerometry measurements improve the accuracy of tonic-clonic seizure detection
Jingwei Zhang, Lauren Swinnen, Christos Chatzichristos, et al.
Annals of Clinical and Translational Neurology
|
May 21, 2021
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy
Stefan Wolking, Claudia Moreau, Mark McCormack, et al.
Epilepsia Open
|
March 15, 2019
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine
Bianca Berghuis, Caragh Stapleton, Anja C M Sonsma, et al.
Journal of Neurochemistry
|
September 14, 2017
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies
Maike F Dohrn, Nicola Glöckle, Lejla Mulahasanovic, et al.
Epilepsia Open
|
December 11, 2019
Genomic and clinical predictors of lacosamide response in refractory epilepsies
Sinéad B Heavin, Mark McCormack, Stefan Wolking, et al.
Epilepsia Open
|
August 24, 2019
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy
Katri Silvennoinen, Nikola de Lange, Sara Zagaglia, et al.
Epilepsia
|
March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medications
Stefan Wolking, Claudia Moreau, Anne T Nies, et al.
Pharmacogenomics
|
April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study
Stefan Wolking, Herbert Schulz, Anne T Nies, et al.
Epilepsia
|
October 17, 2025
Value of ultra-high-field MRI in patients with drug-resistant focal epilepsy and negative 3T MRI (EpiUltraStudy): Diagnostic gain of 7T structural analysis
Rick H G J van Lanen, Daniel Uher, Christianne M C Hoeberigs, et al.
Neurology
|
December 31, 2017
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
Mark McCormack, Hongsheng Gui, Andrés Ingason, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Physiological Measurement
|
May 21, 2024
Multimodal wearable EEG, EMG and accelerometry measurements improve the accuracy of tonic-clonic seizure detection
Jingwei Zhang, Lauren Swinnen, Christos Chatzichristos, et al.
Annals of Clinical and Translational Neurology
|
May 21, 2021
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy
Stefan Wolking, Claudia Moreau, Mark McCormack, et al.
Epilepsia Open
|
March 15, 2019
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine
Bianca Berghuis, Caragh Stapleton, Anja C M Sonsma, et al.
Journal of Neurochemistry
|
September 14, 2017
Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies
Maike F Dohrn, Nicola Glöckle, Lejla Mulahasanovic, et al.
Epilepsia Open
|
December 11, 2019
Genomic and clinical predictors of lacosamide response in refractory epilepsies
Sinéad B Heavin, Mark McCormack, Stefan Wolking, et al.
Epilepsia Open
|
August 24, 2019
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy
Katri Silvennoinen, Nikola de Lange, Sara Zagaglia, et al.
Epilepsia
|
March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medications
Stefan Wolking, Claudia Moreau, Anne T Nies, et al.
Pharmacogenomics
|
April 21, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study
Stefan Wolking, Herbert Schulz, Anne T Nies, et al.
Epilepsia
|
October 17, 2025
Value of ultra-high-field MRI in patients with drug-resistant focal epilepsy and negative 3T MRI (EpiUltraStudy): Diagnostic gain of 7T structural analysis
Rick H G J van Lanen, Daniel Uher, Christianne M C Hoeberigs, et al.
Neurology
|
December 31, 2017
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
Mark McCormack, Hongsheng Gui, Andrés Ingason, et al.
Page
of 6