Epilepsy
"Epilepsy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)
Descriptor ID |
D004827
|
MeSH Number(s) |
C10.228.140.490
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Concept/Terms |
Epilepsy- Epilepsy
- Epilepsies
- Seizure Disorder
- Seizure Disorders
- Seizures, Epileptic
- Epileptic Seizures
- Epileptic Seizure
- Seizure, Epileptic
Single Seizure- Single Seizure
- Seizure, Single
- Seizures, Single
- Single Seizures
Epilepsy, Cryptogenic- Epilepsy, Cryptogenic
- Cryptogenic Epilepsies
- Cryptogenic Epilepsy
- Epilepsies, Cryptogenic
|
Below are MeSH descriptors whose meaning is more general than "Epilepsy".
Below are MeSH descriptors whose meaning is more specific than "Epilepsy".
This graph shows the total number of publications written about "Epilepsy" by people in UAMS Profiles by year, and whether "Epilepsy" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2022 | 14 | 0 | 14 | 2021 | 14 | 0 | 14 | 2020 | 10 | 0 | 10 | 2019 | 12 | 0 | 12 | 2018 | 5 | 1 | 6 | 2017 | 7 | 0 | 7 | 2016 | 5 | 0 | 5 | 2015 | 5 | 0 | 5 | 2014 | 6 | 0 | 6 | 2013 | 2 | 2 | 4 | 2012 | 9 | 0 | 9 | 2011 | 3 | 0 | 3 | 2010 | 6 | 1 | 7 | 2009 | 2 | 1 | 3 | 2008 | 3 | 0 | 3 | 2007 | 4 | 2 | 6 | 2006 | 5 | 0 | 5 | 2005 | 4 | 0 | 4 | 2004 | 1 | 1 | 2 | 2003 | 3 | 1 | 4 | 2002 | 0 | 2 | 2 | 2001 | 1 | 0 | 1 | 2000 | 1 | 0 | 1 | 1998 | 4 | 0 | 4 | 1997 | 1 | 1 | 2 | 1995 | 1 | 0 | 1 | 1994 | 2 | 0 | 2 | 1992 | 1 | 0 | 1 | 1990 | 2 | 0 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Epilepsy" by people in Profiles over the past ten years.
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Samanta D. GRIN2A-related epilepsy and speech disorders: A comprehensive overview with a focus on the role of precision therapeutics. Epilepsy Res. 2023 Jan; 189:107065.
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Samanta D. Recent developments in stereo electroencephalography monitoring for epilepsy surgery. Epilepsy Behav. 2022 10; 135:108914.
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Miceli F, Millevert C, Soldovieri MV, Mosca I, Ambrosino P, Carotenuto L, Schrader D, Lee HK, Riviello J, Hong W, Risen S, Emrick L, Amin H, Ville D, Edery P, de Bellescize J, Michaud V, Van-Gils J, Goizet C, Willemsen MH, Kleefstra T, Møller RS, Bayat A, Devinsky O, Sands T, Korenke GC, Kluger G, Mefford HC, Brilstra E, Lesca G, Milh M, Cooper EC, Taglialatela M, Weckhuysen S. KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism. EBioMedicine. 2022 Jul; 81:104130.
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McLeod GA, Abbasian P, Toutant D, Ghassemi A, Duke T, Rycyk C, Serletis D, Moussavi Z, Ng MC. Sleep-wake states change the interictal localization of candidate epileptic source generators. Sleep. 2022 06 13; 45(6).
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Seo GY, Neal ES, Han F, Vidovic D, Nooru-Mohamed F, Dienel GA, Sullivan MA, Borges K. Brain glycogen content is increased in the acute and interictal chronic stages of the mouse pilocarpine model of epilepsy. Epilepsia Open. 2022 06; 7(2):361-367.
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Sonoda M, Rothermel R, Carlson A, Jeong JW, Lee MH, Hayashi T, Luat AF, Sood S, Asano E. Naming-related spectral responses predict neuropsychological outcome after epilepsy surgery. Brain. 2022 04 18; 145(2):517-530.
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Samanta D. DEPDC5-related epilepsy: A comprehensive review. Epilepsy Behav. 2022 05; 130:108678.
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Samanta D. The role of implementation science in improving epilepsy surgery utilization. Epilepsy Behav. 2022 05; 130:108669.
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Samanta D, Ostendorf AP, Singh R, Gedela S, Elumalai V, Hoyt ML, Perry MS, Bartolini L, Curran GM. Physicians' Perspectives on Presurgical Discussion and Shared Decision-Making in Pediatric Epilepsy Surgery. J Child Neurol. 2022 04; 37(5):416-425.
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Ahrens SM, Ostendorf AP, Lado FA, Arnold ST, Bai S, Bensalem-Owen MK, Chapman KE, Clarke DF, Eisner M, Fountain NB, Gray JM, Gunduz MT, Hopp JL, Riker E, Schuele SU, Small B, Herman ST. Impact of the COVID-19 Pandemic on Epilepsy Center Practice in the United States. Neurology. 2022 05 10; 98(19):e1893-e1901.
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Vanoye CG, Desai RR, Ji Z, Adusumilli S, Jairam N, Ghabra N, Joshi N, Fitch E, Helbig KL, McKnight D, Lindy AS, Zou F, Helbig I, Cooper EC, George AL. High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity. JCI Insight. 2022 03 08; 7(5).
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Boysen S, Elumalai V, ElSheikh RH, Aravindhan A, Veerapandiyan A. Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene. J Clin Neurosci. 2022 06; 100:212-213.
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Serletis D, MacDonald C, Xu Q, Kazina CJ, Dakshinamurti S, Marin S, Del Bigio MR. Hemispherectomy for hemimegalencephaly in a 6.5-week-old infant with tuberous sclerosis complex. Childs Nerv Syst. 2022 07; 38(7):1415-1419.
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Merten JE, Villarrubia SA, Holly KS, Kemp AS, Kumler AC, Larson-Prior LJ, Murray TA. The use of rodent models to better characterize the relationship among epilepsy, sleep, and memory. Epilepsia. 2022 03; 63(3):525-536.
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Samanta D, Elumalai V, Leigh Hoyt M, Modi AC, Sajatovic M. A qualitative study of epilepsy self-management barriers and facilitators in Black children and caregivers in Arkansas. Epilepsy Behav. 2022 01; 126:108491.
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Ostendorf AP, Ahrens SM, Lado FA, Arnold ST, Bai S, Bensalem Owen MK, Chapman KE, Clarke DF, Eisner M, Fountain NB, Gray JM, Hopp JL, Riker E, Schuele SU, Small BV, Herman ST. United States Epilepsy Center Characteristics: A Data Analysis From the National Association of Epilepsy Centers. Neurology. 2022 02 01; 98(5):e449-e458.
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Samanta D, Elumalai V, Desai VC, Hoyt ML. Conceptualization and implementation of an interdisciplinary clinic for children with drug-resistant epilepsy during the COVID-19 pandemic. Epilepsy Behav. 2021 12; 125:108403.
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Alexander H, Govindan RB, Anwar T, Chirumamilla VC, Fayed I, Keating RF, Gaillard WD, Oluigbo CO. Global and intertuberal epileptic networks in tuberous sclerosis based on stereoelectroencephalographic (sEEG) findings: a quantitative EEG analysis in pediatric subjects and surgical implications. Childs Nerv Syst. 2022 02; 38(2):407-419.
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Samanta D, Hoyt ML, Perry MS. Parental experience and decision-making for epilepsy surgery: A systematic review of qualitative and quantitative studies. Epilepsy Behav. 2021 10; 123:108263.
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Samanta D, Beal JC, Grinspan ZM. Automated Identification of Surgical Candidates and Estimation of Postoperative Seizure Freedom in Children - A Focused Review. Semin Pediatr Neurol. 2021 10; 39:100914.
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Mitsuhashi T, Sonoda M, Sakakura K, Jeong JW, Luat AF, Sood S, Asano E. Dynamic tractography-based localization of spike sources and animation of spike propagations. Epilepsia. 2021 10; 62(10):2372-2384.
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Samanta D, Leigh Hoyt M, Scott Perry M. Healthcare professionals' knowledge, attitude, and perception of epilepsy surgery: A systematic review. Epilepsy Behav. 2021 09; 122:108199.
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Wortmann SB, Zietkiewicz S, Guerrero-Castillo S, Feichtinger RG, Wagner M, Russell J, Ellaway C, Mróz D, Wyszkowski H, Weis D, Hannibal I, von Stülpnagel C, Cabrera-Orefice A, Lichter-Konecki U, Gaesser J, Windreich R, Myers KC, Lorsbach R, Dale RC, Gersting S, Prada CE, Christodoulou J, Wolf NI, Venselaar H, Mayr JA, Wevers RA. Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency. Genet Med. 2021 09; 23(9):1705-1714.
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Giménez DeGeorge E, Fullen C, Gess J, Kleiner J, Larson-Prior L. Effects of age of onset and medication on cognitive performance and quality of life in patients with epilepsy. Epilepsy Behav. 2021 08; 121(Pt A):108008.
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Voisin N, Schnur RE, Douzgou S, Hiatt SM, Rustad CF, Brown NJ, Earl DL, Keren B, Levchenko O, Geuer S, Verheyen S, Johnson D, Zarate YA, Hancárová M, Amor DJ, Bebin EM, Blatterer J, Brusco A, Cappuccio G, Charrow J, Chatron N, Cooper GM, Courtin T, Dadali E, Delafontaine J, Del Giudice E, Doco M, Douglas G, Eisenkölbl A, Funari T, Giannuzzi G, Gruber-Sedlmayr U, Guex N, Heron D, Holla ØL, Hurst ACE, Juusola J, Kronn D, Lavrov A, Lee C, Lorrain S, Merckoll E, Mikhaleva A, Norman J, Pradervand S, Prchalová D, Rhodes L, Sanders VR, Sedlácek Z, Seebacher HA, Sellars EA, Sirchia F, Takenouchi T, Tanaka AJ, Taska-Tench H, Tønne E, Tveten K, Vitiello G, Vlcková M, Uehara T, Nava C, Yalcin B, Kosaki K, Donnai D, Mundlos S, Brunetti-Pierri N, Chung WK, Reymond A. Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy. Am J Hum Genet. 2021 05 06; 108(5):857-873.
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Samanta D, Singh R, Gedela S, Scott Perry M, Arya R. Underutilization of epilepsy surgery: Part II: Strategies to overcome barriers. Epilepsy Behav. 2021 04; 117:107853.
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Samanta D, Ostendorf AP, Willis E, Singh R, Gedela S, Arya R, Scott Perry M. Underutilization of epilepsy surgery: Part I: A scoping review of barriers. Epilepsy Behav. 2021 04; 117:107837.
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Kopel J, Grooms A, Ganapathy V, Clothier J. Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: a case of pharmaco-synergistic heterozygosity. Psychiatr Genet. 2021 02 01; 31(1):32-35.
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Klöckner C, Sticht H, Zacher P, Popp B, Babcock HE, Bakker DP, Barwick K, Bonfert MV, Bönnemann CG, Brilstra EH, Chung WK, Clarke AJ, Devine P, Donkervoort S, Fraser JL, Friedman J, Gates A, Ghoumid J, Hobson E, Horvath G, Keller-Ramey J, Keren B, Kurian MA, Lee V, Leppig KA, Lundgren J, McDonald MT, McLaughlin HM, McTague A, Mefford HC, Mignot C, Mikati MA, Nava C, Raymond FL, Sampson JR, Sanchis-Juan A, Shashi V, Shieh JTC, Shinawi M, Slavotinek A, Stödberg T, Stong N, Sullivan JA, Taylor AC, Toler TL, van den Boogaard MJ, van der Crabben SN, van Gassen KLI, van Jaarsveld RH, Van Ziffle J, Wadley AF, Wagner M, Wigby K, Wortmann SB, Zarate YA, Møller RS, Lemke JR, Platzer K. De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy. Genet Med. 2021 04; 23(4):653-660.
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Samanta D. Recent Advances in the Diagnosis and Treatment of Neonatal Seizures. Neuropediatrics. 2021 04; 52(2):73-83.
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Stamberger H, Hammer TB, Gardella E, Vlaskamp DRM, Bertelsen B, Mandelstam S, de Lange I, Zhang J, Myers CT, Fenger C, Afawi Z, Almanza Fuerte EP, Andrade DM, Balcik Y, Ben Zeev B, Bennett MF, Berkovic SF, Isidor B, Bouman A, Brilstra E, Busk ØL, Cairns A, Caumes R, Chatron N, Dale RC, de Geus C, Edery P, Gill D, Granild-Jensen JB, Gunderson L, Gunning B, Heimer G, Helle JR, Hildebrand MS, Hollingsworth G, Kharytonov V, Klee EW, Koeleman BPC, Koolen DA, Korff C, Küry S, Lesca G, Lev D, Leventer RJ, Mackay MT, Macke EL, McEntagart M, Mohammad SS, Monin P, Montomoli M, Morava E, Moutton S, Muir AM, Parrini E, Procopis P, Ranza E, Reed L, Reif PS, Rosenow F, Rossi M, Sadleir LG, Sadoway T, Schelhaas HJ, Schneider AL, Shah K, Shalev R, Sisodiya SM, Smol T, Stumpel CTRM, Stuurman K, Symonds JD, Mau-Them FT, Verbeek N, Verhoeven JS, Wallace G, Yosovich K, Zarate YA, Zerem A, Zuberi SM, Guerrini R, Mefford HC, Patel C, Zhang YH, Møller RS, Scheffer IE. NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns. Genet Med. 2021 02; 23(2):363-373.
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Samanta D. Epilepsy in Angelman syndrome: A scoping review. Brain Dev. 2021 Jan; 43(1):32-44.
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Kuruva M, Moncayo VM, Peterson RB. PET and SPECT Imaging of Epilepsy: Technical Considerations, Pathologies, and Pitfalls. Semin Ultrasound CT MR. 2020 Dec; 41(6):551-561.
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McKenzie MB, Jones ML, O'Carroll A, Serletis D, Shafer LA, Ng MC. Breakthrough spikes in rapid eye movement sleep from the epilepsy monitoring unit are associated with peak seizure frequency. Sleep. 2020 05 12; 43(5).
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French JA, Brodie MJ, Caraballo R, Devinsky O, Ding D, Jehi L, Jette N, Kanner A, Modi AC, Newton CR, Patel AA, Pennell PB, Perucca E, Sander JW, Scheffer IE, Singh G, Williams E, Wilmshurst J, Cross JH. Keeping people with epilepsy safe during the COVID-19 pandemic. Neurology. 2020 06 09; 94(23):1032-1037.
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Lewis H, Samanta D, Örsell JL, Bosanko KA, Rowell A, Jones M, Dale RC, Taravath S, Hahn CD, Krishnakumar D, Chagnon S, Keller S, Hagebeuk E, Pathak S, Bebin EM, Arndt DH, Alexander JJ, Mainali G, Coppola G, Maclean J, Sparagana S, McNamara N, Smith DM, Raggio V, Cruz M, Fernández-Jaén A, Kava MP, Emrick L, Fish JL, Vanderver A, Helman G, Pierson TM, Zarate YA. Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome. Pediatr Neurol. 2020 11; 112:94-100.
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Birnbaum AK, Meador KJ, Karanam A, Brown C, May RC, Gerard EE, Gedzelman ER, Penovich PE, Kalayjian LA, Cavitt J, Pack AM, Miller JW, Stowe ZN, Pennell PB. Antiepileptic Drug Exposure in Infants of Breastfeeding Mothers With Epilepsy. JAMA Neurol. 2020 04 01; 77(4):441-450.
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Samanta D. Levetiracetam is Still Not a First-line Treatment in Neonatal Seizures. Indian Pediatr. 2020 01 15; 57(1):80.
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Samanta D. Ketamine in Refractory Neonatal Seizures. Pediatr Neurol. 2020 05; 106:76.
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Motoi H, Jeong JW, Juhász C, Miyakoshi M, Nakai Y, Sugiura A, Luat AF, Sood S, Asano E. Quantitative analysis of intracranial electrocorticography signals using the concept of statistical parametric mapping. Sci Rep. 2019 11 22; 9(1):17385.
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Symonds JD, Zuberi SM, Stewart K, McLellan A, O'Regan M, MacLeod S, Jollands A, Joss S, Kirkpatrick M, Brunklaus A, Pilz DT, Shetty J, Dorris L, Abu-Arafeh I, Andrew J, Brink P, Callaghan M, Cruden J, Diver LA, Findlay C, Gardiner S, Grattan R, Lang B, MacDonnell J, McKnight J, Morrison CA, Nairn L, Slean MM, Stephen E, Webb A, Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort. Brain. 2019 08 01; 142(8):2303-2318.
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Desai R, Singh S, Patel U, Fong HK, Kaur VP, Varma Y, Madan D, Patel S, Mahuwala Z, Sachdeva R, Kumar G. Frequency of takotsubo cardiomyopathy in epilepsy-related hospitalizations among adults and its impact on in-hospital outcomes: A national standpoint. Int J Cardiol. 2020 01 15; 299:67-70.
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Luat AF, Juhász C, Loeb JA, Chugani HT, Falchek SJ, Jain B, Greene-Roethke C, Amlie-Lefond C, Ball KL, Davis A, Pinto A. Neurological Complications of Sturge-Weber Syndrome: Current Status and Unmet Needs. Pediatr Neurol. 2019 09; 98:31-38.
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Vargason T, Frye RE, McGuinness DL, Hahn J. Clustering of co-occurring conditions in autism spectrum disorder during early childhood: A retrospective analysis of medical claims data. Autism Res. 2019 08; 12(8):1272-1285.
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Tse K, Hammond D, Simpson D, Beynon RJ, Beamer E, Tymianski M, Salter MW, Sills GJ, Thippeswamy T. The impact of postsynaptic density 95 blocking peptide (Tat-NR2B9c) and an iNOS inhibitor (1400W) on proteomic profile of the hippocampus in C57BL/6J mouse model of kainate-induced epileptogenesis. J Neurosci Res. 2019 11; 97(11):1378-1392.
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Samanta D, Ramakrishnaiah R, Schaefer B. The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy. Acta Neurol Belg. 2020 Apr; 120(2):447-450.
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Dizon MLV, Rao R, Hamrick SE, Zaniletti I, DiGeronimo R, Natarajan G, Kaiser JR, Flibotte J, Lee KS, Smith D, Yanowitz T, Mathur AM, Massaro AN. Practice variation in anti-epileptic drug use for neonatal hypoxic-ischemic encephalopathy among regional NICUs. BMC Pediatr. 2019 02 27; 19(1):67.
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Wong VSS, Stevenson M, Mott J, Sahaya K. Seizure and epilepsy publication in nonneurology journals. Epilepsy Behav. 2019 04; 93:7-11.
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Nakai Y, Sugiura A, Brown EC, Sonoda M, Jeong JW, Rothermel R, Luat AF, Sood S, Asano E. Four-dimensional functional cortical maps of visual and auditory language: Intracranial recording. Epilepsia. 2019 02; 60(2):255-267.
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Avery E, MacDonald C, Ng M, Serletis D. Survey of epilepsy and seizure awareness in Manitoba: An evaluation. Epilepsy Behav. 2019 03; 92:195-199.
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Kumar A, Juhász C, Luat A, Govil-Dalela T, Behen ME, Hicks MA, Chugani HT. Evolution of Brain Glucose Metabolic Abnormalities in Children With Epilepsy and SCN1A Gene Variants. J Child Neurol. 2018 11; 33(13):832-836.
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Voinescu PE, Park S, Chen LQ, Stowe ZN, Newport DJ, Ritchie JC, Pennell PB. Antiepileptic drug clearances during pregnancy and clinical implications for women with epilepsy. Neurology. 2018 09 25; 91(13):e1228-e1236.
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Motoi H, Miyakoshi M, Abel TJ, Jeong JW, Nakai Y, Sugiura A, Luat AF, Agarwal R, Sood S, Asano E. Phase-amplitude coupling between interictal high-frequency activity and slow waves in epilepsy surgery. Epilepsia. 2018 10; 59(10):1954-1965.
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Chen S, Joodi G, Devinsky O, Sadaf MI, Pursell IW, Simpson RJ. Under-reporting of sudden unexpected death in epilepsy. Epileptic Disord. 2018 Aug 01; 20(4):270-278.
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Song J, Swallow E, Said Q, Peeples M, Meiselbach M, Signorovitch J, Kohrman M, Korf B, Krueger D, Wong M, Sparagana S. Epilepsy treatment patterns among patients with tuberous sclerosis complex. J Neurol Sci. 2018 08 15; 391:104-108.
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Luat AF, Behen ME, Chugani HT, Juhász C. Cognitive and motor outcomes in children with unilateral Sturge-Weber syndrome: Effect of age at seizure onset and side of brain involvement. Epilepsy Behav. 2018 03; 80:202-207.
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Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G, FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, Andrade DM, Rossignol E, Minassian BA, Michaud JL. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. Am J Hum Genet. 2017 Nov 02; 101(5):664-685.
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Kambara T, Sood S, Alqatan Z, Klingert C, Ratnam D, Hayakawa A, Nakai Y, Luat AF, Agarwal R, Rothermel R, Asano E. Presurgical language mapping using event-related high-gamma activity: The Detroit procedure. Clin Neurophysiol. 2018 01; 129(1):145-154.
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Schartz ND, Wyatt-Johnson SK, Price LR, Colin SA, Brewster AL. Status epilepticus triggers long-lasting activation of complement C1q-C3 signaling in the hippocampus that correlates with seizure frequency in experimental epilepsy. Neurobiol Dis. 2018 Jan; 109(Pt A):163-173.
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Thygesen SK, Olsen M, Pedersen L, Henderson VW, Østergaard JR, Sørensen HT. Respiratory distress syndrome in preterm infants and risk of epilepsy in a Danish cohort. Eur J Epidemiol. 2018 03; 33(3):313-321.
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Bank AM, Stowe ZN, Newport DJ, Ritchie JC, Pennell PB. Placental passage of antiepileptic drugs at delivery and neonatal outcomes. Epilepsia. 2017 05; 58(5):e82-e86.
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Fitzgerald RT, Santoro J, Hinduja A, Samant RS, Kumar M, Angtuaco EJ. PRES and Epilepsy: A Potential Long-Term Consequence of a "Reversible" Syndrome. Neurologist. 2017 Mar; 22(2):41-43.
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Zheng F. TRPC Channels and Epilepsy. Adv Exp Med Biol. 2017; 976:123-135.
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Luat AF, Coyle L, Kamat D. The Ketogenic Diet: A Practical Guide for Pediatricians. Pediatr Ann. 2016 Dec 01; 45(12):e446-e450.
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Couch CG, Menendez ME, Barnes CL. Perioperative Risk in Patients With Epilepsy Undergoing Total Joint Arthroplasty. J Arthroplasty. 2017 02; 32(2):537-540.
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Wilson TA, Rodgers S, Tanweer O, Agarwal P, Lieber BA, Agarwal N, McDowell M, Devinsky O, Weiner H, Harter DH. Tuberous Sclerosis Health Care Utilization Based on the National Inpatient Sample Database: A Review of 5655 Hospitalizations. World Neurosurg. 2016 Jul; 91:97-105.
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Samanta D. A 15-year-old with seizures: late diagnosis of pyridoxine-dependent epilepsy. Acta Neurol Belg. 2016 Dec; 116(4):667-669.
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Samanta D. Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy. Neurol India. 2016 Mar-Apr; 64(2):327-8.
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Olsen M, Thygesen SK, Østergaard JR, Nielsen H, Henderson VW, Ehrenstein V, Nørgaard M, Sørensen HT. Hospital-Diagnosed Pertussis Infection in Children and Long-term Risk of Epilepsy. JAMA. 2015 Nov 03; 314(17):1844-9.
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Gupta HV, Vengoechea J, Sahaya K, Virmani T. A splice site mutation in ATP6AP2 causes X-linked intellectual disability, epilepsy, and parkinsonism. Parkinsonism Relat Disord. 2015 Dec; 21(12):1473-5.
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Soltesz I, Alger BE, Kano M, Lee SH, Lovinger DM, Ohno-Shosaku T, Watanabe M. Weeding out bad waves: towards selective cannabinoid circuit control in epilepsy. Nat Rev Neurosci. 2015 May; 16(5):264-77.
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Sharp GB, Samanta D, Willis E. Options for pharmacoresistant epilepsy in children: when medications don't work. Pediatr Ann. 2015 Feb; 44(2):e43-8.
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Haddad N, Grant I, Eswaran H. Telemedicine for patients with epilepsy: a pilot experience. Epilepsy Behav. 2015 Mar; 44:1-4.
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Frye RE. Metabolic and mitochondrial disorders associated with epilepsy in children with autism spectrum disorder. Epilepsy Behav. 2015 Jun; 47:147-57.
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Albert GW, Ibrahim GM, Otsubo H, Ochi A, Go CY, Snead OC, Drake JM, Rutka JT. Magnetoencephalography-guided resection of epileptogenic foci in children. J Neurosurg Pediatr. 2014 Nov; 14(5):532-7.
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Serletis D, Bulacio J, Bingaman W, Najm I, González-Martínez J. The stereotactic approach for mapping epileptic networks: a prospective study of 200 patients. J Neurosurg. 2014 Nov; 121(5):1239-46.
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Vattoth S, Manzil FF, Singhal A, Riley KO, Bag AK. State of the art epilepsy imaging: an update. Clin Nucl Med. 2014 Jun; 39(6):511-23; quiz 524-6.
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Kehrl JM, Sahaya K, Dalton HM, Charbeneau RA, Kohut KT, Gilbert K, Pelz MC, Parent J, Neubig RR. Gain-of-function mutation in Gnao1: a murine model of epileptiform encephalopathy (EIEE17)? Mamm Genome. 2014 Jun; 25(5-6):202-10.
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Johnson EL, Stowe ZN, Ritchie JC, Newport DJ, Newman ML, Knight B, Pennell PB. Carbamazepine clearance and seizure stability during pregnancy. Epilepsy Behav. 2014 Apr; 33:49-53.
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Mundt JC, Greist JH, Jefferson JW, Federico M, Mann JJ, Posner K. Prediction of suicidal behavior in clinical research by lifetime suicidal ideation and behavior ascertained by the electronic Columbia-Suicide Severity Rating Scale. J Clin Psychiatry. 2013 Sep; 74(9):887-93.
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Aboud O, Mrak RE, Boop FA, Griffin WS. Epilepsy: neuroinflammation, neurodegeneration, and APOE genotype. Acta Neuropathol Commun. 2013 Jul 29; 1:41.
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