Results 71 to 80 of about 5,863 (207)
A variant of idiopathic epilepsy: Clinical note
Неврология, нейропсихиатрия, психосоматика, 2015 The paper describes a clinical case of idiopathic generalized epilepsy with a variable phenotype, a similar type of epileptiform activity in the second stage of sleep, and a similar genotype in siblings.
V. A. Karlov +3 more
doaj +1 more source
Trends in antiseizure medication monotherapy for pediatric epilepsy in the United States
Epilepsia Open, Volume 11, Issue 3, Page 1028-1035, June 2026.Abstract Objective National prescribing trends for antiseizure medication (ASM) in children with epilepsy over the past decade are unclear. Despite the 2021 SANAD II trials supporting lamotrigine and valproate for focal and generalized epilepsies, respectively, it is unknown if their use increased.
Adam P. Ostendorf +6 more
wiley +1 more source
Clinical genetic study in juvenile myoclonic epilepsy
, 2014 PurposeTo evaluate clinical features of probands with juvenile myoclonic epilepsy (JME) and affected members of their families in order to study clinical genetics of JME.MethodThirteen unrelated families with at least two members with history of seizures
Kuzmanovski, Igor +2 more
core +1 more source
Carbamazepine-Induced Juvenile Myoclonic Seizures
Pediatric Neurology Briefs, 2000 The risk of aggravation of juvenile myoclonic epilepsy (JME) among 40 of 170 consecutive patients who had received carbamazepine (CBZ) or phenytoin (PHT) was determined at the Centre Saint Paul, Marseille, and the Clinique Neurologique, Hopital Pasteur ...
J Gordon Millichap
doaj +1 more source
Journal of Ardabil University of Medical Sciences, 2017 Background & objectives: Epilepsy is a chronic neurological disorder that disrupts normal brain activity due to abnormal electrical discharge of brain cells. Mood swings, depression and anxiety are the common complications in epilepsy.
Zarife Sohrabi +4 more
doaj
A case of juvenile myoclonic epilepsy in which a disease‐specific question led to the diagnosis
Journal of General and Family Medicine, 2022 A 17‐year‐old female patient presented to our hospital with repeated transient loss of consciousness lasting less than 10 min. After regaining consciousness, she experienced no disorientation, confusion, tongue‐biting, or incontinence. Physical findings,
Hiroki Maita +4 more
doaj +1 more source
Epilepsia, Volume 67, Issue 5, Page 2601-2612, May 2026.Abstract Objective This study was undertaken to evaluate whether synaptic vesicle protein 2A (SV2A) expression on peripheral immune cells predicts treatment response to levetiracetam in epilepsy. Methods High‐dimensional flow cytometry was used to prospectively assess SV2A expression on immune cells from levetiracetam responders, nonresponders, and ...
Johannes Lang +4 more
wiley +1 more source
Clinical Epidemiology, 2022 Magnus Spangsberg Boesen,1 Melita Cacic Hribljan,2 Søren Kirchhoff Christensen,1 Amalie Wandel Klein-Petersen,3 Sahla El Mahdaoui,4 Malini Vendela Sagar,5 Emilie Schou,5 Anna Korsgaard Eltvedt,6 Malene Landbo Børresen,3,7 Maria Jose Miranda,6 Alfred ...
Boesen MS +12 more
doaj
Неврология, 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
Pregnancy, Volume 2, Issue 3, May 2026.Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld +5 more
wiley +1 more source