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Epilepsia|July 12, 2012
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrumKarl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Epilepsia|April 14, 2010
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3Sarah E Heron, Ingrid E Scheffer, Bronwyn E Grinton, et al.
Developmental Medicine and Child Neurology|June 16, 2020
Focal epilepsy in SCN1A-mutation carrying patients: is there a role for epilepsy surgery?Aikaterini Vezyroglou, Sophia Varadkar, Thomas Bast, et al.
Journal of Child Neurology|December 6, 2011
Thoracic myelopathy secondary to seizure following scoliosis surgeryKenneth A Myers, Eric T Payne, Michael J Esser, et al.
Scientific Reports|April 14, 2018
A cell surface display fluorescent biosensor for measuring MMP14 activity in real-timeAlexander Braun, Matthew J Farber, Zachary A Klase, et al.
Neurology. Clinical Practice|September 28, 2020
Clinical utility of therapeutic drug monitoring of antiepileptic drugs: Systematic reviewZanab Al-Roubaie, Elena Guadagno, Agnihotram V Ramanakumar, et al.
The Journal of Cell Biology|January 26, 2011
Distinct ECM mechanosensing pathways regulate microtubule dynamics to control endothelial cell branching morphogenesisKenneth A Myers, Kathryn T Applegate, Gaudenz Danuser, et al.
Journal of Child Neurology|March 24, 2022
Focal Epilepsy in Children With Tuberous Sclerosis Complex: Does Vigabatrin Control Focal Seizures?Sufang Lin, Jianxiang Liao, Xia Zhao, et al.
Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
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