Results 71 to 80 of about 69,249 (312)

VARIANTS OF THE GENERALIZATION OF EPILEPTIC SEIZURES IN MESIAL TEMPORAL EPILEPSY IN ADULTS

Эпилепсия и пароксизмальные состояния, 2016
The purpose of work was to study polymorphism of kinematic variants of secondary generalized convulsive seizures by research of lesional and non-lesional mesial temporal epilepsy. For this purpose the patients suffering by non-lesional variants of mesial
V. О. Generalov, Т. R. Sadykov, Yu. ВV. Kazakova, Е. V. Amcheslavskaya   +3 more
doaj  

Psychoses of epilepsy: A study comparing the clinical features of patients with focal versus generalized epilepsies

, 2011
In the literature, psychosis of epilepsy (POE) has been described as one of the most frequent psychiatric comorbidities of epilepsy, occurring particularly in association with temporal lobe epilepsy.
SILVA, Joyce Macedo da, Yacubian, Elza Márcia Targas [UNIFESP], YACUBIAN, Elza Marcia T., Silva, Joyce Macedo da [UNIFESP], MARCHETTI, Renato Luis, Gerardo Maria de Araújo Filho, Lenon Mazetto, MAZETTO, Lenon, Joyce Macedo da Silva, Renato Luis Marchetti, ARAUJO FILHO, Gerardo Maria de, Elza Márcia T. Yacubian, Araujo Filho, Gerardo Maria de [UNIFESP], Mazetto, Lenon [UNIFESP]   +13 more
core   +1 more source

Screening Routine Clinical Notes for Epilepsy Surgery Candidates Using Large Language Models

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epilepsy surgery is severely underutilized despite proven efficacy, with substantial under‐referral of eligible patients in routine clinical practice. This study evaluated the potential role of large language models (LLMs) as decision‐support tools for screening unstructured clinical notes to identify epilepsy surgery candidates and ...
Uriel Fennig, Nadav Amir, Maya Schiller, Roni Loebenstein, Johnatan Nissan, Marina Boxer, Shany Guly Gofrit, Gal Goshen, Sándor Beniczky, Nicola Maggio   +9 more
wiley   +1 more source

Early Recognition of Treatment‐Responsive Rapidly Progressive Dementia: The Modified STAM3mP Score

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Early identification of patients with treatment‐responsive rapidly progressive dementia (RPD) is important as early treatment improves outcomes. The STAM3P score identifies treatment‐responsive RPD using “high risk” presenting features. We optimized performance by adding a time component (i.e., dementia within 3 months) and validated the ...
R. W. van Steenhoven, N. Satyadev, A. E. M. Bastiaansen, Y. D. Piura, J. Kerstens, Y. S. Crijnen, J. Brenner, T. Brand, T. M. Bienfait, S. Veenbergen, J. M. de Vries, F. J. de Jong, E. G. P. Dopper, P. A. E. Sillevis Smitt, H. Seelaar, G. S. Day, M. J. Titulaer   +16 more
wiley   +1 more source

Epilepsy in Christianson syndrome: Two cases of Lennox–Gastaut syndrome and a review of literature

Epilepsy & Behavior Reports, 2020
Christianson syndrome (CS) is an X-linked intellectual disorder caused by mutations in the SLC9A6 gene. Clinical features of CS include an inability to speak, truncal ataxia, postnatal microcephaly, hyperkinesis, and epilepsy. Almost all patients with CS
Azusa Ikeda, Ayako Yamamoto, Kazushi Ichikawa, Yu Tsuyusaki, Megumi Tsuji, Mizue Iai, Yumi Enomoto, Hiroaki Murakami, Kenji Kurosawa, Satoko Miyatake, Naomichi Matsumoto, Tomohide Goto   +11 more
doaj   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source

Relationship Between Medication Adherence and Prospective Memory in Individuals with Epilepsy

Archives of Epilepsy
Objective: Epilepsy is a condition characterized by sudden, recurrent epileptic seizures that occur as a result of abnormal and excessive electrical discharge in cortical neurons and are not triggered by an identifiable event.
Ece Hilal, Yağmur Uluhan, Serkan Aksu, Semai Bek, Gülnihal Kutlu   +4 more
doaj   +1 more source

Role of genetics in the etiopathogenesis of genetic generalized epilepsy: A review of current literature

Sahel Medical Journal, 2016
Until recently, genetic generalized epilepsy (GGE) was believed to be of presumed genetic etiology with no identifiable genetic mutation or demonstrable epigenetic abnormality. A wide range of epileptic disorders has clue for an inherited susceptibility.
S A Balarabe, M M Watila
doaj   +1 more source

Impaired language function in generalized epilepsy : Inadequate suppression of the default mode network

, 2013
We aimed to study the effect of a potential default mode network (DMN) dysfunction on language performance in epilepsy. Language dysfunction in focal epilepsy has previously been connected to brain damage in language-associated cortical areas.
McAllister, Anita, Ulrici, Daniel,, McAllister, Anita,, Landtblom, Anne-Marie,, Karlsson, Thomas,, van Ettinger-Veenstra, Helene,, Landtblom, Anne-Marie, Gauffin, Helena, van Ettinger-Veenstra, Helene, Karlsson, Thomas, Ulrici, Daniel, Engström, Maria, Engström, Maria,, Gauffin, Helena,   +13 more
core   +1 more source

Prominent Movement Disorders in RNU2‐2‐Related Spliceosomopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Pediatric movement disorders often overlap with neurodevelopmental diseases, suggesting shared molecular mechanisms. Variants in small nuclear RNA (snRNA) genes encoding spliceosome components have recently been associated with neurodevelopmental disorders, termed “RNUopathies.” We analyzed genome sequencing data from 14 patients with ...
Magdalena Krygier, Ugo Sorrentino, Matias Wagner, Marta Zawadzka, Anna Lemska, Maria Mazurkiewicz‐Bełdzińska, Michael Zech   +6 more
wiley   +1 more source