Results 81 to 90 of about 713,420 (262)

Localizing value of ictal déjà vu, déjà vécu, dreamy state and reminiscence: A systematic review

Epileptic Disorders, EarlyView.
Abstract We performed a systematic review of the literature regarding the localization value of déjà vu (DV), déjà vécu, dreamy state and reminiscence in focal epilepsy, with the aim to summarize the state‐of‐the‐art anatomo‐electroclinical correlations in the field and help guide interpretation of ictal semiology within the framework of pre‐surgical ...
Amir Janah, Lilach Goldstein, Firas Fahoum   +2 more
wiley   +1 more source

Seizure-Induced Miosis

Pediatric Neurology Briefs, 2012
Researchers at University of Southampton, UK report an infant with focal seizures secondary to cortical dysplasia who presented at age 4 months with bilateral pinpoint pupils as first feature of right-sided clonic seizure.
J Gordon Millichap
doaj   +1 more source

Localizing value of ecstatic phenomenon in epilepsy surgery: A systematic review

Epileptic Disorders, EarlyView.
Abstract Objective A systematic review was conducted to synthesize current anatomo‐clinical correlations of ecstatic symptoms in focal epilepsy, aiming to provide evidence‐based guidance for interpreting this ictal semiology during presurgical evaluation.
Mihai Dragos Maliia, Fabrice Bartolomei, Fabienne Picard   +2 more
wiley   +1 more source

Focal Cortical Dysplasias

Journal of the International Child Neurology Association, 2017
Focal cortical dysplasias (FCDs) are common malformations of cerebral cortical development that are highly associated with medically intractable epilepsy. FCDs have been classified according to neuropathological subtypes (type Ia, Ib, IIA, IIb, and III) based on the severity of cytoarchitectural disruption, and the presence of unique cell types (e.g ...
Ali Mahta, Peter B. Crino
openaire   +2 more sources

Utility of Double Inversion Recovery Sequences in MRI

Pediatric Neurology Briefs, 2016
Investigators from the Mayo Clinic, Rochester Minnesota investigated the utility of three-dimensional (3D) double inversion recovery (DIR) sequences in magnetic resonance imaging (MRI) detection of focal cortical dysplasia (FCD) in children and young ...
Maura E. Ryan
doaj   +1 more source

Cortical neuronal loss and hippocampal sclerosis are not detected by voxel-based morphometry in individual epilepsy surgery patients [PDF]

, 2009
Voxel-based morphometry (VBM) has detected differences between brains of groups of patients with epilepsy and controls, but the sensitivity for detecting subtle pathological changes in single subjects has not been established.
Martinian, Lillian, Sisodiya, Sanjay M., John S. Duncan, Sisodiya, S.M., Mark R. Symms, Niels K. Focke, Eriksson, Sofia H., Sofia H. Eriksson, Lillian Martinian, Focke, N.K., Thom, M., Duncan, John S., Martinian, L., Duncan, J.S., Symms, Mark R., Thom, Maria, Symms, M.R., Maria Thom, Focke, Niels K., Eriksson, S.H., Sanjay M. Sisodiya   +20 more
core   +1 more source

Pediatric new‐onset seizure‐like events: Yield of diagnostic work‐up

Epileptic Disorders, EarlyView.
Abstract Objective To assess the diagnostic yield of ancillary investigations in children presenting with new‐onset seizure‐like events (SLEs) at a tertiary first seizure clinic (FSC). Methods We conducted a retrospective cohort study including 1213 children evaluated for new‐onset SLEs at a tertiary FSC.
Geertruida Slinger, Lotte Noorlag, Willem M. Otte, Maeike Zijlmans, Rosalie L. Neijzen, Sandra M. A. van der Salm, Floor E. Jansen, Kees P. J. Braun, Eric van Diessen   +8 more
wiley   +1 more source

Ulnar focal cortical indentation: a progressive, deforming variant of focal fibrocartilaginous dysplasia.

, 2019
BACKGROUND: Focal fibrocartilaginous dysplasia is a rare growth disturbance of bone resulting in deformity. In the ulna, focal fibrocartilaginous dysplasia is particularly rare, and the characteristic fibroligamentous tether can result in progressive ...
Rapp, Jordan, Ali, Sayed, Fenerty, Sarah, MD, Zlotolow, Dan A, Gershkovich, Grigory, Goldbach, Alyssa R   +5 more
core   +1 more source

PI3K/AKT Pathway and Brain Malformations

Pediatric Neurology Briefs, 2015
Investigators from Seattle Children's Research Institute, University of Washington, and collaborating institutions sought to evaluate 10 genes in the PI3K/AKT pathway as it relates epileptogenic brain malformations in patients with megalencephaly ...
Gavin B. Rice, Nitin R. Wadhwani
doaj   +1 more source

Pragmatic screening for autoimmune‐associated epilepsy in drug‐resistant epilepsy of unknown etiology in resource‐limited settings: A hypothesis‐generating study

Epileptic Disorders, EarlyView.
Abstract Objective To evaluate the feasibility of investigating autoimmune etiology in adults with drug‐resistant epilepsy (DRE) of unknown origin in resource‐limited settings and to develop a pragmatic, hypothesis‐generating screening approach to guide autoantibody testing. Methods A prospective observational study including adults with DRE of unknown
Tomásia O. de H. M. Frezatti, Ricardo L. Saute, Veriano Alexandre Júnior, Frederico N. Nakano, Marina T. R. P. Dalio, Tonicarlo R. Velasco, João P. Leite, Antônio Carlos dos Santos, Vanessa D. Marques, Américo C. Sakamoto   +9 more
wiley   +1 more source