Results 221 to 230 of about 2,345,783 (392)

TUBA1A‐related tubulinopathy associated with the infantile epileptic spasms syndrome and atypical absence seizures

Epileptic Disorders, EarlyView.
Abstract Patients with TUBA1A pathogenic variants may present with complex brain malformation, intellectual disability, and epilepsy. The epilepsy phenotype is varied, ranging from mild to severe, with epileptic spasms and focal seizures being the most common seizure types.
Andy Cheuk‐Him Ng, Morris H. Scantlebury   +1 more
wiley   +1 more source

Infantile epileptic spasm syndrome: predictors of short- and long-term outcomes. [PDF]

Front Pediatr
Al-Omari MA, Chavez-Castillo M, Miller MR, Prasad AN, Nouri MN.   +4 more
europepmc   +1 more source

Creativity and its link to epilepsy

Epilepsia Open, EarlyView.
Abstract Creative thinking represents one of our highest‐order cognitive processes, involving multiple cortical structures and an intricate interplay between several cortical and subcortical networks. It results in novel ideas that translate to useful products or concepts. The evolutionary purpose of creativity is therefore apparent, as it advances our
Itay Tokatly Latzer, Phillip L. Pearl
wiley   +1 more source

Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?

, 2009
Eylert Brodtkorb, T. Torbergsen, Karl O. Nakken, Andersen Kv, R. Gimse, Ottar Sjaastad   +5 more
openalex   +1 more source

Acquired epileptic opercular syndrome related to a heterozygous deleterious substitution in GRIN2A [PDF]

, 2017
Claudine Sculier, Anne-Sophie Tilmant, Xavier De Tiège, Sanda Giurgea, Philippe Paquier, Gabrielle Rudolf, Gaëtan Lesca, Patrick Van Bogaert   +7 more
openalex   +1 more source

Inherited metabolic epilepsies–established diseases, new approaches

Epilepsia Open, EarlyView.
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley   +1 more source

Evaluation, Diagnosis, and Treatment of Concomitant Movement Disorders in Genetic Epilepsies. [PDF]

Epilepsy Curr
Garris J, Abbott M, Axeen E, Tochen L, Schreiber JM.   +4 more
europepmc   +1 more source

Immediate versus delayed detection of Takotsubo syndrome after epileptic seizures [PDF]

, 2018
Claudia Stöllberger, Markus Sauerberg, Josef Finsterer   +2 more
openalex   +1 more source

Takotsubo cardiomyopathy during armed conflict: A case series

ESC Heart Failure, Volume 12, Issue 2, Page 1494-1498, April 2025.
Sharon Bruoha, Artyom Star, Gili Givaty, Michael Shilo, Michael Friger, Vladimir Chitoroga, Hezzy Shmueli, Yigal Abramowitz, Elad Asher, Jamal Jafari, Vladimir Shlyakhover, Doron Zahger, Moti Haim, Chaim Yosefy   +13 more
wiley   +1 more source

Comparative assessment of artificial intelligence chatbots' performance in responding to healthcare professionals' and caregivers' questions about Dravet syndrome

Epilepsia Open, EarlyView.
Abstract Objective Artificial intelligence chatbots have been a game changer in healthcare, providing immediate, round‐the‐clock assistance. However, their accuracy across specific medical domains remains under‐evaluated. Dravet syndrome remains one of the most challenging epileptic encephalopathies, with new data continuously emerging in the ...
Joana Jesus‐Ribeiro, Eugenia Roza, Bárbara Oliveiros, Joana Barbosa Melo, Mar Carreño   +4 more
wiley   +1 more source