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Brenda Porter - Publications

Affiliations: 
Stanford University, Palo Alto, CA 
Area:
Neurology
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22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.326
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  0.379
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  0.309
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  0.331
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  0.365
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  0.334
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  0.342
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  0.32
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  0.301
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  0.339
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  0.313
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  0.339
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  0.372
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  0.342
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  0.359
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  0.355
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  0.362
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  0.323
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  0.306
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