208 results on '"Archer, John S."'
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2. Cognition, adaptive skills and epilepsy disability/severity in patients with Lennox–Gastaut syndrome undergoing deep brain stimulation for epilepsy in the ESTEL trial
3. Frontoparietal 18F-FDG-PET hypo-metabolism in Lennox-Gastaut syndrome: Further evidence highlighting the key network
4. Targeted therapeutic mild hypercapnia after cardiac arrest: A phase II multi-centre randomised controlled trial (the CCC trial)
5. Pontine and cerebral atrophy in Lennox–Gastaut syndrome
6. The epileptic network of Lennox-Gastaut syndrome: Cortically driven and reproducible across age
7. Paroxysmal fast activity is a biomarker of treatment response in deep brain stimulation for Lennox–Gastaut syndrome
8. 2295 Changes in the burden of generalised fast epileptiform activity predict changes in clinical seizure frequency in patients with Lennox-Gastaut syndrome
9. 2296 Cognition, adaptive skills and epilepsy disability/severity in patients with Lennox-Gastaut syndrome undergoing deep brain stimulation for epilepsy
10. Thalamocortical functional connectivity in Lennox–Gastaut syndrome is abnormally enhanced in executive‐control and default‐mode networks
11. The Optimal Target and Connectivity for Deep Brain Stimulation in Lennox–Gastaut Syndrome
12. A neurodevelopmental basis for BECTS: Evidence from structural MRI
13. Abnormal neurovascular coupling during status epilepticus migrainosus in Sturge-Weber syndrome
14. Response: Can ECT cause “kindling” in the human brain ?
15. DBS of Thalamic Centromedian Nucleus for Lennox–Gastaut Syndrome (ESTEL Trial)
16. Abnormal cognitive network interactions in Lennox-Gastaut syndrome: A potential mechanism of epileptic encephalopathy
17. Epileptic encephalopathy: Use and misuse of a clinically and conceptually important concept
18. Brain regions with abnormal network properties in severe epilepsy of Lennox-Gastaut phenotype: Multivariate analysis of task-free fMRI
19. Focal epileptiform spikes do not show a canonical BOLD response in patients with benign rolandic epilepsy (BECTS)
20. Lennox-Gastaut syndrome and phenotype: Secondary network epilepsies
21. Tonic seizures of Lennox-Gastaut syndrome: Periictal single-photon emission computed tomography suggests a corticopontine network
22. DBS of Thalamic Centromedian Nucleus for Lennox–Gastaut Syndrome (ESTEL Trial).
23. Cortex leads the thalamic centromedian nucleus in generalized epileptic discharges in Lennox‐Gastaut syndrome
24. Combined Isoflurane-Remifentanil Anaesthesia Permits Resting-State fMRI in Children with Severe Epilepsy and Intellectual Disability
25. Automatic detection of generalized paroxysmal fast activity in Lennox-Gastaut syndrome using a bi-modal EEG time-frequency feature
26. Small temporal pole encephaloceles: A treatable cause of “lesion negative” temporal lobe epilepsy
27. Targeting the centromedian thalamic nucleus for deep brain stimulation
28. Neuropsychological and functional MRI studies provide converging evidence of anterior language dysfunction in BECTS
29. Supplemental Material for: The epileptic network of Lennox-Gastaut syndrome: cortically driven and reproducible across age
30. Event-related fMRI of Myoclonic Jerks Arising from Dysplastic Cortex
31. Stable ratio of ipsilateral to contralateral sensory motor cortex activity despite varying effort and peripheral nerve block
32. fMRI “deactivation” of the posterior cingulate during generalized spike and wave
33. Benign Epilepsy with Centro-temporal Spikes: Spike Triggered fMRI Shows Somato-sensory Cortex Activity
34. Intraoperative definition of bottom-of-sulcus dysplasia using intraoperative ultrasound and single depth electrode recording – A technical note
35. A Sheep Model for the Study of Focal Epilepsy with Concurrent Intracranial EEG and Functional MRI
36. Editorial: Functional Brain Mapping of Epilepsy Networks: Methods and Applications
37. Refractory focal motor seizures controlled with intramuscular botulinum toxin
38. Hemiconvulsion-hemiplegia-epilepsy evolving to contralateral hemi-Lennox-Gastaut-like phenotype
39. Cognitive network reorganization following surgical control of seizures in Lennox-Gastaut syndrome
40. Brief asymmetric tonic posturing with diffuse low-voltage fast activity in seizures arising from the mesial parietal region
41. Abnormal neurovascular coupling during status epilepticus migrainosus in Sturge-Weber syndrome
42. CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures
43. Constructing Carbon Fiber Motion-Detection Loops for Simultaneous EEG–fMRI
44. Conceptualizing Lennox–Gastaut Syndrome as a Secondary Network Epilepsy
45. Functional MRI interactions between dysplastic nodules and overlying cortex in periventricular nodular heterotopia
46. Tonic seizures ofLennox‐Gastaut syndrome: Periictal single‐photon emission computed tomography suggests a corticopontine network
47. Murray Valley encephalitis: a review of clinical features, diagnosis and treatment
48. Suboptimal anti-epilepsy drug use is common among Indigenous patients with seizures presenting to the emergency department
49. ACUTE HIPPOCAMPAL SCLEROSIS FOLLOWING ECSTASY INGESTION
50. Wernicke’s encephalopathy mimicking variant Creutzfeldt-Jakob disease
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