Year |
Citation |
Score |
2024 |
Vossler DG, Porter BE, Kira R, Lee J, Aeby A, Patten A, Cheng JY, Ngo LY. Efficacy and safety of perampanel in patients with seizures associated with Lennox-Gastaut syndrome: A randomized trial. Epilepsia. PMID 39576191 DOI: 10.1111/epi.18193 |
0.32 |
|
2021 |
Pavitt S, Carley A, Porter B, Knowles JK. A Standardized Protocol to Improve Acute Seizure Management in Hospitalized Pediatric Patients. Hospital Pediatrics. PMID 33685859 DOI: 10.1542/hpeds.2020-000968 |
0.325 |
|
2020 |
Yang QZ, Spelbrink EM, Nye KL, Hsu ER, Porter BE. Epilepsy and EEG Phenotype of SLC13A5 Citrate Transporter Disorder. Child Neurology Open. 7: 2329048X20931361. PMID 32551328 DOI: 10.1177/2329048X20931361 |
0.378 |
|
2020 |
Madani N, O'Malley JA, Porter BE, Baumer FM. Lacosamide-Induced Dyskinesia in Children With Intractable Epilepsy. Journal of Child Neurology. 883073820926634. PMID 32524876 DOI: 10.1177/0883073820926634 |
0.31 |
|
2020 |
Grayson LE, Peters JM, McPherson T, Krueger DA, Sahin M, Wu JY, Northrup HA, Porter B, Cutter GR, O'Kelley SE, Krefting J, Stone SS, Madsen JR, Fallah A, Blount JP, et al. Pilot Study of Neurodevelopmental Impact of Early Epilepsy Surgery in Tuberous Sclerosis Complex. Pediatric Neurology. PMID 32418847 DOI: 10.1016/J.Pediatrneurol.2020.04.002 |
0.334 |
|
2018 |
Tomlinson SB, Khambhati AN, Bermudez C, Kamens RM, Heuer GG, Porter BE, Marsh ED. Alterations of network synchrony after epileptic seizures: An analysis of post-ictal intracranial recordings in pediatric epilepsy patients. Epilepsy Research. 143: 41-49. PMID 29655171 DOI: 10.1016/J.Eplepsyres.2018.04.003 |
0.363 |
|
2018 |
Baumer FM, Porter BE. Clinical and electrographic features of sunflower syndrome. Epilepsy Research. 142: 58-63. PMID 29555355 DOI: 10.1016/j.eplepsyres.2018.03.002 |
0.332 |
|
2018 |
Knowles JK, Santoro JD, Porter BE, Baumer FM. Refractory focal epilepsy in a paediatric patient with primary familial brain calcification. Seizure. 56: 50-52. PMID 29448117 DOI: 10.1016/j.seizure.2018.02.001 |
0.359 |
|
2017 |
Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, ... ... Porter B, et al. Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies. Brain : a Journal of Neurology. 140: 2337-2354. PMID 29050392 DOI: 10.1093/Brain/Awx184 |
0.327 |
|
2017 |
Bainbridge MN, Cooney E, Miller M, Kennedy AD, Wulff JE, Donti T, Jhangiani SN, Gibbs RA, Elsea SH, Porter BE, Graham BH. Analyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycle. Molecular Genetics and Metabolism. PMID 28673551 DOI: 10.1016/J.Ymgme.2017.06.009 |
0.34 |
|
2017 |
Lee S, Fisher P, Grant GA, Porter B, Dannenberg B, Wintermark M. R-SCAN: Imaging for Pediatric Simple Febrile Seizures. Journal of the American College of Radiology : Jacr. PMID 28551342 DOI: 10.1016/J.Jacr.2017.04.007 |
0.321 |
|
2017 |
Tomlinson SB, Porter BE, Marsh ED. Interictal network synchrony and local heterogeneity predict epilepsy surgery outcome among pediatric patients. Epilepsia. PMID 28166392 DOI: 10.1111/Epi.13657 |
0.302 |
|
2016 |
Tomlinson SB, Bermudez C, Conley C, Brown MW, Porter BE, Marsh ED. Spatiotemporal Mapping of Interictal Spike Propagation: A Novel Methodology Applied to Pediatric Intracranial EEG Recordings. Frontiers in Neurology. 7: 229. PMID 28066315 DOI: 10.3389/Fneur.2016.00229 |
0.338 |
|
2016 |
Klotz J, Porter BE, Colas C, Schlessinger A, Pajor AM. Mutations in the Na(+)/citrate cotransporter NaCT (SLC13A5) in pediatric patients with epilepsy and developmental delay. Molecular Medicine (Cambridge, Mass.). 22. PMID 27261973 DOI: 10.2119/Molmed.2016.00077 |
0.312 |
|
2015 |
Zhu X, Dubey D, Bermudez C, Porter BE. Suppressing cAMP response element-binding protein transcription shortens the duration of status epilepticus and decreases the number of spontaneous seizures in the pilocarpine model of epilepsy. Epilepsia. PMID 26419901 DOI: 10.1111/epi.13211 |
0.337 |
|
2015 |
Skjei KL, Church EW, Harding BN, Santi M, Holland-Bouley KD, Clancy RR, Porter BE, Heuer GG, Marsh ED. Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy. Journal of Neurosurgery. Pediatrics. 1-7. PMID 26339958 DOI: 10.3171/2015.5.Peds14551 |
0.37 |
|
2013 |
Porter BE, Jacobson C. Report of a parent survey of cannabidiol-enriched cannabis use in pediatric treatment-resistant epilepsy. Epilepsy & Behavior : E&B. 29: 574-7. PMID 24237632 DOI: 10.1016/j.yebeh.2013.08.037 |
0.341 |
|
2013 |
Paciorkowski AR, Traylor RN, Rosenfeld JA, Hoover JM, Harris CJ, Winter S, Lacassie Y, Bialer M, Lamb AN, Schultz RA, Berry-Kravis E, Porter BE, Falk M, Venkat A, Vanzo RJ, et al. MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways. Neurogenetics. 14: 99-111. PMID 23389741 DOI: 10.1007/S10048-013-0356-Y |
0.318 |
|
2012 |
Huang C, Marsh ED, Ziskind DM, Celix JM, Peltzer B, Brown MW, Storm PB, Litt B, Porter BE. Leaving tissue associated with infrequent intracranial EEG seizure onsets is compatible with post-operative seizure freedom. Journal of Pediatric Epilepsy. 1: 211-219. PMID 24563805 DOI: 10.3233/Pep-12033 |
0.358 |
|
2011 |
Gupta JR, Marsh ED, Nieh HA, Porter BE, Litt B. Discrete gamma oscillations identify the seizure onset zone in some pediatric epilepsy patients. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2011: 3095-8. PMID 22254994 DOI: 10.1109/IEMBS.2011.6090845 |
0.354 |
|
2010 |
Marsh ED, Peltzer B, Brown MW, Wusthoff C, Storm PB, Litt B, Porter BE. Interictal EEG spikes identify the region of electrographic seizure onset in some, but not all, pediatric epilepsy patients. Epilepsia. 51: 592-601. PMID 19780794 DOI: 10.1111/J.1528-1167.2009.02306.X |
0.361 |
|
2008 |
Porter BE. Neurogenesis and epilepsy in the developing brain. Epilepsia. 49: 50-4. PMID 18522600 DOI: 10.1111/j.1528-1167.2008.01637.x |
0.322 |
|
2003 |
Porter BE, Judkins AR, Clancy RR, Duhaime A, Dlugos DJ, Golden JA. Dysplasia: a common finding in intractable pediatric temporal lobe epilepsy. Neurology. 61: 365-8. PMID 12913199 DOI: 10.1212/01.Wnl.0000076487.28227.6E |
0.305 |
|
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