Results 91 to 100 of about 643,938 (290)
The syndrome of limbic encephalitis is a severe clinical condition with heterogenous aetiopathogenesis. A common pathogen causing the infectious syndrome of limbic encephalitis is herpes simplex virus (HSV), but rare cases caused by Treponema pallidum ...
Eliška Marešová +4 more
doaj +1 more source
Pathologic tearfulness after limbic encephalitis
Objective We investigated the nature and neural foundations of pathologic tearfulness in a uniquely large cohort of patients who had presented with autoimmune limbic encephalitis (aLE). Methods We recruited 38 patients (26 men, 12 women; median age 63.06
Georgios P. D. Argyropoulos +8 more
semanticscholar +1 more source
Epilepsy syndromes classification
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell +4 more
wiley +1 more source
Abstract Objective Late‐onset unexplained epilepsy (LoUE), defined as epilepsy onset after age 55 without an obvious cause, is an important risk factor for dementia. Studies have shown that 10%–25% of individuals with LoUE develop dementia within 3–4 years following their first seizure.
Alice D. Lam +13 more
wiley +1 more source
Anti-Hu limbic encephalitis preceding the appearance of mediastinal germinoma by 9 years
Autoimmune limbic encephalitis is characterized by the subacute onset of seizures, short-term memory loss, and confusion and can have a paraneoplastic or nonparaneoplastic etiology.1 Anti-Hu limbic encephalitis is typically paraneoplastic, most ...
Matthew Silsby +3 more
semanticscholar +1 more source
Distinct medial temporal volumetric signatures in extra‐medial temporal lobe lesional epilepsy
Abstract Objective To quantify amygdala and hippocampal volumetric asymmetries in patients with drug‐resistant epilepsy (DRE) and extra‐medial temporal lesions (EMTLs) and to assess the prevalence of structural alterations relative to drug‐resistant temporal lobe epilepsy (TLE), extratemporal lobe epilepsy (ETLE), and healthy individuals.
Yonatan Serlin +7 more
wiley +1 more source
Non-herpetic Acute Limbic Encephalitis: a New Subgroup of Limbic Encephalitis?
Hiroshi Shoji1, Noriyuki Kimura2, Toshihide Kumamoto2, Takashi Ichiyama3 and Yukitoshi Takahashi4 1Division of Neurology, St. Mary Hospital, Fukuoka 830-8543, 2Department of Internal Medicine III, Faculty of Medicine, Oita University, Oita, 3Department of Pediatrics, Yamaguchi University Graduate School of Medicine, Yamaguchi, 4National Epilepsy Center,
Hiroshi, Shoji +4 more
openaire +3 more sources
Abstract Objective To define and articulate research priorities in epilepsy identified by the European Reference Network for Rare and Complex Epilepsies (ERN EpiCARE), addressing key unmet needs across the spectrum of rare and complex epilepsies. Methods This position paper was developed through a structured collaborative process involving patient ...
Sébile Tchaicha +27 more
wiley +1 more source
Limbic Encephalitis Driven by a Pleural Mesothelioma: A Paraneoplastic Complication
Paraneoplastic neurological syndromes have only been described with pleural mesothelioma in five cases. We have described a 72-year-old man who developed anterograde amnesia 27 months after diagnosis of epithelioid pleural mesothelioma. Investigations
Jacob O. Day, Adam J. Zeman
doaj
Objective Limbic encephalitis associated with antibodies to components of the voltage-gated potassium channel complex (VGKCC-Ab-LE) often leads to hippocampal atrophy and persistent memory impairment.
C. Loane +9 more
semanticscholar +1 more source

