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Page 1
Expert opinion: Proposed diagnostic and treatment algorithms for Lennox-Gastaut syndrome in adult patients.
Montouris G, Aboumatar S, Burdette D, Kothare S, Kuzniecky R, Rosenfeld W, Chung S. Montouris G, et al. Epilepsy Behav. 2020 Sep;110:107146. doi: 10.1016/j.yebeh.2020.107146. Epub 2020 Jun 18. Epilepsy Behav. 2020. PMID: 32563898 Free article. Review.
While the characteristics of LGS in pediatric patients are well defined, including "drop attacks", interictal slow spike and wave electroencephalogram (EEG) activity, and intellectual disability, these features can evolve over time, and different EEG activiti …
While the characteristics of LGS in pediatric patients are well defined, including "drop attacks", interictal slow spike and wave ele …
Poststroke seizure: optimising its management.
Xu MY. Xu MY. Stroke Vasc Neurol. 2018 Dec 9;4(1):48-56. doi: 10.1136/svn-2018-000175. eCollection 2019 Mar. Stroke Vasc Neurol. 2018. PMID: 31105979 Free PMC article. Review.
The use of continuous electroencephalogram has demonstrated significant benefits in capturing interictal or ictal abnormalities, especially in cases of non-convulsive seizures and non-convulsive status epilepticus. ...
The use of continuous electroencephalogram has demonstrated significant benefits in capturing interictal or ictal abnormalities …
Treatment of Seizures and Postanoxic Status Epilepticus.
Reynolds AS, Claassen J. Reynolds AS, et al. Semin Neurol. 2017 Feb;37(1):33-39. doi: 10.1055/s-0036-1593862. Epub 2017 Feb 1. Semin Neurol. 2017. PMID: 28147416 Review.
Postanoxic seizures may be nonconvulsive and very difficult to diagnose without electroencephalography (EEG) or associated with prominent myoclonus. Importantly, to date no randomized controlled trials are available to guide the management of seizures in patients wi …
Postanoxic seizures may be nonconvulsive and very difficult to diagnose without electroencephalography (EEG) or associated wit …
Clinical management of epileptic encephalopathies of childhood and infancy.
Covanis A. Covanis A. Expert Rev Neurother. 2014 Jun;14(6):687-701. doi: 10.1586/14737175.2014.919854. Expert Rev Neurother. 2014. PMID: 24852231 Review.
Epileptic encephalopathies represent a group of devastating epileptic disorders that appear early in life and are characterized by pharmacoresistant generalized or focal seizures, persistent severe EEG abnormalities, and cognitive dysfunction or decline. The ictal a …
Epileptic encephalopathies represent a group of devastating epileptic disorders that appear early in life and are characterized by pharmacor …
Treatment of Epileptic Encephalopathies: Current State of the Art.
Nariai H, Duberstein S, Shinnar S. Nariai H, et al. J Child Neurol. 2018 Jan;33(1):41-54. doi: 10.1177/0883073817690290. Epub 2017 Jan 30. J Child Neurol. 2018. PMID: 28134012 Free PMC article. Review.
Childhood epileptic encephalopathies are age-dependent disorders of the brain whose hallmarks include loss of neurologic function over time, abnormal electroencephalographic findings, and seizures. Ictal and interictal electrographic activity are conjointly thought …
Childhood epileptic encephalopathies are age-dependent disorders of the brain whose hallmarks include loss of neurologic function over time, …
The utility of ambulatory electroencephalography in routine clinical practice: a critical review.
Seneviratne U, Mohamed A, Cook M, D'Souza W. Seneviratne U, et al. Epilepsy Res. 2013 Jul;105(1-2):1-12. doi: 10.1016/j.eplepsyres.2013.02.004. Epub 2013 Mar 13. Epilepsy Res. 2013. PMID: 23490658 Review.
Over the last four decades, ambulatory electroencephalography (EEG) has evolved to be a useful tool in the diagnosis of epilepsy and certain nonepileptic paroxysmal disorders. ...It appears superior to routine EEG in capturing interictal abnormaliti …
Over the last four decades, ambulatory electroencephalography (EEG) has evolved to be a useful tool in the diagnosis of epilep …
Stereo-EEG Evaluation and Surgical Treatment in Patients With Drug-Resistant Focal Epilepsy Associated With Nodular Heterotopia.
Durica SR, Caruso JP, Podkorytova I, Ding K, Hays R, Lega B, Perven G. Durica SR, et al. J Clin Neurophysiol. 2023 Jan 1;40(1):17-26. doi: 10.1097/WNP.0000000000000850. Epub 2021 Apr 7. J Clin Neurophysiol. 2023. PMID: 34009845
RESULTS: Of the six patients who underwent nine laser interstitial thermal therapy procedures either in isolation or in combination with other surgical therapies, four patients were Engel Ia, one was Engel IIb, and one was Engel IIIa, with an average follow-up of 22 …
RESULTS: Of the six patients who underwent nine laser interstitial thermal therapy procedures either in isolation or in combination w …
Management of seizures in Lennox-Gastaut syndrome.
Crumrine PK. Crumrine PK. Paediatr Drugs. 2011 Apr 1;13(2):107-18. doi: 10.2165/11536940-000000000-00000. Paediatr Drugs. 2011. PMID: 21351810 Review.
Examples of causes of Lennox-Gastaut syndrome include migrational abnormalities of the brain, late effects of CNS infections, certain genetic disorders such as tuberous sclerosis, and inherited metabolic disorders. The difficulty early in the course of Lennox-Gastaut syndr …
Examples of causes of Lennox-Gastaut syndrome include migrational abnormalities of the brain, late effects of CNS infections, certain …
Mesial temporal sclerosis: pathogenesis, diagnosis, and management.
Gates JR, Cruz-Rodriguez R. Gates JR, et al. Epilepsia. 1990;31 Suppl 3:S55-66. doi: 10.1111/j.1528-1157.1990.tb05860.x. Epilepsia. 1990. PMID: 2226372 Review.
The majority of patients (78%) with postresection MTS who are seizure-free have tightly localized interictal abnormalities restricted to F7/F8, Sp1/Sp2, T3/T4, and T5/T6 more than 96% of the time. MRI abnormalities may be seen in 55% of patients with MTS if b …
The majority of patients (78%) with postresection MTS who are seizure-free have tightly localized interictal abnormalities res …
Emerging neuroimaging contribution to the diagnosis and management of the ring chromosome 20 syndrome.
Vaudano AE, Ruggieri A, Vignoli A, Canevini MP, Meletti S. Vaudano AE, et al. Epilepsy Behav. 2015 Apr;45:155-63. doi: 10.1016/j.yebeh.2015.02.002. Epub 2015 Apr 3. Epilepsy Behav. 2015. PMID: 25843339 Review.
Based on the available lines of evidences, [r(20)] syndrome is characterized by interictal and ictal dysfunctions within basal ganglia-prefrontal lobe networks and by long-lasting effects of the peculiar theta-delta rhythm, which represents an EEG marker of the synd …
Based on the available lines of evidences, [r(20)] syndrome is characterized by interictal and ictal dysfunctions within basal gangli …
34 results