Results 111 to 120 of about 353,788 (280)

Clinical and Electrical Evolution of “Pseudo” Spike–Wave Activation in Sleep EEG Patterns in Self-Limited Childhood Epilepsies

Annals of Indian Academy of Neurology
The purpose of this study was to identify the pseudo spike–wave activation in sleep (SWAS) patterns in the electroencephalogram (EEG) of self-limited focal epilepsies of childhood (SeLFE) and study their clinical and electrical evolution.
Neetha Balaram, Smita Balachandran, Abdul V Gafoor, SR Ratheesh   +3 more
doaj   +1 more source

Teratogenicity and Antiseizure Medications

Epilepsy Currents, 2020
openaire   +2 more sources

Methodological challenges in pregnancy pharmacoepidemiology : the case of antiseizure medication and offspring neurodevelopment [Elektronisk resurs]

This thesis is driven by the overarching aim of elucidating methodological challenges inherent in pharmacoepidemiology during pregnancy, with a particular focus on antiseizure medications.
Ahlqvist, VH,
core  

Antiseizure medications and their differing effects on cardiovascular risk

Epilepsy & Behavior Reports
This review discusses the differing effects of enzyme-inducing and non-inducing antiseizure medications on cardiovascular risk and their implications for the management strategies of epilepsy patients. Traditional risk markers, including low density lipoprotein, high density lipoprotein and triglycerides, can be altered by both enzyme induction and ...
Aleena Abbasi, Bassil Abbasi, Scott Mintzer, Carla LoPinto-Khoury   +3 more
openaire   +3 more sources

Sustained seizure freedom with fenfluramine for refractory epilepsy due to 7q32‐q34 deletion syndrome

Epileptic Disorders, EarlyView.
Divya Veerapaneni, Abdulrahman Bukhari, Irfan S. Sheikh   +2 more
wiley   +1 more source

Dietary patterns in children with epilepsy: The role of household environment and clinical comorbidities

Epileptic Disorders, EarlyView.
Abstract Objective To evaluate dietary patterns in children with epilepsy and compare them with age‐ and sex‐matched healthy siblings living in the same household environment. Associations between clinical characteristics and dietary adequacy were also examined.
Ana Claudia Cândido Oliveira, Maria Eduarda Pereira Santana, Giuliane V. M. Zanin, Jaqueline Lamas da Silva, Camila Borelli Zeller, Ana Carolina Coan   +5 more
wiley   +1 more source

Antiseizure medication use during pregnancy and children’s neurodevelopmental outcomes

Nature Communications
The teratogenic potential of valproate in pregnancy is well established; however, evidence regarding the long-term safety of other antiseizure medications (ASMs) during pregnancy remains limited.
Paul Madley-Dowd, Viktor H. Ahlqvist, Harriet Forbes, Jessica E. Rast, Florence Z. Martin, Caichen Zhong, Ciarrah-Jane S. Barry, Daniel Berglind, Michael Lundberg, Kristen Lyall, Craig J. Newschaffer, Torbjörn Tomson, Neil M. Davies, Cecilia Magnusson, Dheeraj Rai, Brian K. Lee   +15 more
doaj   +1 more source

Clinical burden and treatment patterns associated with Dravet or Lennox-Gastaut syndromes: A retrospective study using natural language processing of narrative unstructured electronic health records

Heliyon
Introduction: This study aimed to investigate the clinical and humanistic burden in two developmental and epileptic encephalopathies, Dravet syndrome and Lennox-Gastaut syndrome, and describe challenges related to treatment with antiseizure medications ...
Mei Lu, Dave Iwanyckyj, Sally W. Wade, Pablo Racana, Fernando Otalora, Satish Rao   +5 more
doaj   +1 more source

Functional/dissociative seizures as a manifestation of forced normalization in eyelid myoclonia with absence epilepsy

Epileptic Disorders, EarlyView.
Fernando Vasquez‐Lopez, Jimena Gonzalez‐Salido, Salvador Martínez‐Medina, Irving Fuentes‐Calvo, Diego A. Barrios‐González, Betsy C. Vázquez‐Cruz, Juan Carlos Vera‐López, Jimena Colado‐Martinez, Orelli Ruiz‐Rodríguez, Pilar Robles‐Lomelin, Maximiliano Salgado Deza, Diego A. Hernandez, Álvaro José Moreno Avellán, Mario A. Sebastián Díaz, Daniel Crail‐Meléndez, Ángel Ruiz‐Chow, Iris E. Martínez‐Juárez   +16 more
wiley   +1 more source

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

Epileptic 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, Evripidis Pityrigkas, Zoi Kallia, Georgia Pepe, Antonis Frontistis, Dimitrios Profer, Vasilios Kimiskidis   +6 more
wiley   +1 more source