Results 141 to 150 of about 171,584 (263)

Reflex seizures and epilepsy surgery: A network approach case‐based exploration

open access: yesEpileptic Disorders, EarlyView.
Abstract Context Reflex seizures (RS) are defined by their consistent provocation by specific stimuli, encompassing a broad range from elementary sensory inputs to complex cognitive tasks. While RS are often encountered in clinical practice, their surgical management remains sparsely reported and poorly systematized.
Olivier Aron   +6 more
wiley   +1 more source

Electroclinical phenotypes—genetic characterization of developmental and epileptic encephalopathies in a cohort study

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by refractory seizures and frequently recurring epileptic activity with neurodevelopmental delay or regression that usually begin in early life. We aimed to define the relationship between electroclinical features and etiology, as well as the genotype–phenotype ...
Burcu Yaman   +7 more
wiley   +1 more source

Localizing value of verbal automatisms, vocal automatisms, singing, and humming: A systematic review

open access: yesEpileptic Disorders, EarlyView.
Abstract Objective We performed a systematic review of the localizing and lateralizing value of verbal automatisms, vocal automatisms, ictal singing, and humming in focal epilepsy with the view to summarize the state‐of‐the‐art clinico‐anatomical correlations in the field and help guide interpretation of ictal semiology within the framework of ...
Vit Vsiansky, Martin Pail, Milan Brazdil
wiley   +1 more source

Unique EEG signature of atypical absence seizures in SYNGAP1‐related developmental and epileptic encephalopathy

open access: yes
Epileptic Disorders, EarlyView.
Rainier Mark Loidor L. Rapal   +2 more
wiley   +1 more source

KBG syndrome: A scoping review of electroclinical features of patients with epilepsy

open access: yesEpileptic Disorders, EarlyView.
Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini   +6 more
wiley   +1 more source

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

open access: yesEpileptic 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   +2 more
wiley   +1 more source

Synchronous Multifocal Intraductal Tubulopapillary Neoplasm of the Pancreas Treated with Total Pancreatectomy: A Case Report. [PDF]

open access: yesSurg Case Rep
Suto K   +11 more
europepmc   +1 more source

EEG findings in SERAC1‐related MEGD(H)EL syndrome

open access: yes
Epileptic Disorders, EarlyView.
Apurva Patel, Dalila Lewis, Thomas Koch
wiley   +1 more source

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