Results 61 to 70 of about 4,695 (177)

Features of the Gestation Course, Delivery, and Postpartum Period in Women with Juvenile Myoclonic Epilepsy

open access: yesНеврология, нейропсихиатрия, психосоматика, 2014
We analyzed 42 pregnancy, delivery, and postpartum period records in women with juvenile myoclonic epilepsy (JME). In most cases, the course of JME was favorable during pregnancy; so administration of subtherapeutic dosages of AEDs in the first and ...
A. V. Yakunina
doaj   +1 more source

The causal relationship between systemic lupus erythematosus and juvenile myoclonic epilepsy: A Mendelian randomization study and mediation analysis

open access: yesIbrain, Volume 11, Issue 1, Page 98-105, Spring 2025.
Mendelian randomization (MR) studies were conducted using the inverse‐variance weighted (IVW) method, MR‐Egger and weighted median on juvenile myoclonic epilepsy (JME), and systemic lupus erythematosus (SLE) data from the Integrative Epidemiology Unit (IEU) Open genome‐wide association study (GWAS) database and the International League Against Epilepsy
Sirui Chen   +10 more
wiley   +1 more source

Acetazolamide Monotherapy for Myoclonic Epilepsy

open access: yesPediatric Neurology Briefs, 1990
Chronic acetazolamide monotherapy controlled generalized tonic-clonic seizures in 14 of 31 patients with juvenile myoclonic-86-epilepsy treated in the Department of Neurology, Columbia University College of Physicians and Surgeons, New York, NY, and the ...
J Gordon Millichap
doaj   +1 more source

Movement Disorders in Developmental and Epileptic Encephalopathies

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Monogenic developmental and epileptic encephalopathies (DEE) frequently feature co‐occurring movement disorders. Gene discovery has expanded epilepsy‐dyskinesia syndromes (EDS) from classic associations such as stereotypies in Rett syndrome to PRRT2‐related infantile seizures with paroxysmal dyskinesia and crouched gait in SCN1A ...
Shekeeb Mohammad   +2 more
wiley   +1 more source

The network neuropsychology of juvenile myoclonic epilepsy

open access: yesCortex
Unknown in the clinical neuropsychology of Juvenile Myoclonic Epilepsy (JME) is the impact of the disorder on the nature of the relationships of specific cognitive abilities among themselves including their patterns of integration, segregation, and topographical organization-that is, the network neuropsychology of JME remains to be addressed.
Camille Garcia-Ramos   +8 more
openaire   +2 more sources

Association Between a Body Shape Index and Epilepsy Among US Adults: Potential Indirect Pathway Through Depressive Symptoms

open access: yesBrain and Behavior, Volume 16, Issue 8, August 2026.
ABSTRACT Background Epilepsy is a common and disabling brain disorder. Whether a body shape index (ABSI) is associated with epilepsy, and whether depressive symptoms may partly account for this association, remain unclear. Methods We analyzed 13,066 participants from the National Health and Nutrition Examination Survey 2013–2018.
Qiaoduan Feng   +6 more
wiley   +1 more source

Clinical utility and genetic landscape of exome sequencing in a large pediatric epilepsy cohort: Insights from a Turkish tertiary care center

open access: yesEpileptic Disorders, Volume 28, Issue 4, Page 1252-1273, August 2026.
Abstract Objective To evaluate the diagnostic utility and genetic spectrum of next‐generation sequencing (NGS) in a large, well‐phenotyped cohort of Turkish pediatric patients with epilepsy of unknown etiology. Methods Between January 2021 and December 2024, 250 children (115 female, 135 male) with unexplained epilepsy underwent either whole‐exome ...
Derya Karaer   +4 more
wiley   +1 more source

Thalamocortical Structural and Functional Connectivity in Juvenile Myoclonic Epilepsy

open access: yesPediatric Neurology Briefs, 2013
Researchers at King’s College, Institute of Psychiatry, London and other centers in the UK, US, and Germany discovered changes in an anterior thalamo-cortical bundle during tests of structural connectivity, as measured by diffusion tensor imaging, in a ...
J Gordon Millichap
doaj   +1 more source

Astrocytes in Genetic Epilepsies: Supporting Actor or Key Player?

open access: yesJournal of Neuroscience Research, Volume 104, Issue 8, August 2026.
Astrocytes contribute to the pathophysiology of acquired epilepsy. However, less is known about their contribution to genetic epilepsy syndromes which often exhibit frequent comorbidity with neurodevelopmental and psychiatric disorders. Epileptic seizures are also frequently present in neurodevelopmental disorders.
Jenny Lange   +4 more
wiley   +1 more source

Epilepsy phenotype in patients with Xp22.31 microduplication

open access: yesEpilepsy and Behavior Case Reports, 2019
The clinical significance of Xp22.31 microduplication is still unclear. We describe a family in which a mother and two children have Xp22.31 microduplication associated with different forms of epilepsy and epileptiform EEG abnormalities.
Mario Brinciotti   +5 more
doaj   +1 more source

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