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Jurnal

Epilepsy & Behavior Reports

Scopus

ISSN 2589-9864 · Elsevier · 526 artikel di indeks

  1. Artikel Jurnal

    Duolingo-induced seizures in GAD65 IgG associated autoimmune epilepsy

    Reece M. Hass; Divyanshu Dubey; Jamie J. Van Gompel dkk.

    Epilepsy & Behavior Reports, Vol. 33 · 2026 · Inggris · DOAJ Scopus

    Autoimmune etiologies of seizures have been increasingly recognized with the discovery of novel autoantibodies to cell surface and intracellular antigens. GAD65 neurologic autoimmunity has been associated with stiff person syndrome, cerebellar ataxia, and chronic focal epilepsy, usually of temporal…

  2. Artikel Jurnal

    Influence of cannabis use on length of stay in patients admitted to the epilepsy monitoring unit

    Oliver Hoerth; Ejerzain Aniles-Renova; Nan Zhang dkk.

    Epilepsy & Behavior Reports, Vol. 33 · 2026 · Inggris · DOAJ Scopus

    Purpose: Epilepsy affects approximately 50 million people worldwide, many of whom undergo evaluation in Epilepsy Monitoring Units (EMUs) for seizure classification, medication management, or presurgical assessment. With increasing numbers of states legalizing marijuana use, a growing number of EMU…

  3. Artikel Jurnal

    Interictal focal epileptic discharges in a pediatric patient with absence status epilepsy: a mimicker of focal epilepsy

    Kento Ohta; Go Yoshino; Masami Togawa dkk.

    Epilepsy & Behavior Reports, Vol. 33 · 2026 · Inggris · DOAJ Scopus

    Absence status epilepsy (ASE) is a rare generalized epilepsy that usually manifests in adolescence or adulthood, although pediatric-onset cases have also been described. It is characterized by recurrent episodes of absence status epilepticus, presenting as prolonged confusion or unresponsiveness…

  4. Artikel Jurnal

    “I’m lonely”: An underrecognized marker of silent suffering in PWE in underresourced settings?

    Amza Ali

    Epilepsy & Behavior Reports, Vol. 33 · 2026 · Inggris · DOAJ Scopus

    Loneliness is increasingly recognized as a significant psychosocial determinant of health, yet it remains comparatively underexplored in the context of epilepsy, and particularly in under-resourced environments. Unlike depression or anxiety, loneliness is less specifically sought, nor readily…

  5. Artikel Jurnal

    Bloodletting as a harmful and misguided first-aid response to seizures in sub-saharan Africa: a case-based review

    Gloire Chubaka Magala; Jamiilah Neve Nchare; Abel Christian Tanoh dkk.

    Epilepsy & Behavior Reports, Vol. 33 · 2026 · Inggris · DOAJ Scopus

    Epileptic seizures are common neurological events whose sociocultural interpretations have long been linked to supernatural causes or biomagico-symbolic beliefs. Depending on the region, blood may be regarded as the cause, seat, vector of evil, or even a therapeutic agent. These misconceptions…

  6. Artikel Jurnal

    Factors associated with epileptiform discharges in patients visiting a memory clinic: A retrospective study

    Katsunori Yokoi; Masashi Tsujimoto; Keisuke Suzuki dkk.

    Epilepsy & Behavior Reports, Vol. 33 · 2026 · Inggris · DOAJ Scopus

    Epilepsy is a common comorbidity in older adults, particularly those with neurodegenerative diseases such as Alzheimer’s disease. However, recognizing epilepsy in patients with dementia can be challenging, as its symptoms often mimic cognitive fluctuations. Reliable clinical indicators validated by…

  7. Artikel Jurnal

    Association of depression and epilepsy in rural northern Rwanda: a prospective longitudinal study with a patient-centered approach

    D.E. Teuwen; P. Dedeken; J. Kayirangwa dkk.

    Epilepsy & Behavior Reports, Vol. 36 · 2026 · Inggris · DOAJ Scopus

    Introduction: Depression is the most frequent co-morbidity in persons living with epilepsy (PwE). In Rwanda, the prevalence of epilepsy ranges between 2.9 and 7.6% and the prevalence of any depression in PwE is more than 22%. This prospective interventional patient-centered study determined…

  8. Artikel Jurnal

    Drug-resistant epilepsy in an autosomal recessive copper metabolism disorder from SLC33A1 mutation

    Raunak Singh; Cheng Yen Kuo; Shelja Sharma dkk.

    Epilepsy & Behavior Reports, Vol. 36 · 2026 · Inggris · DOAJ Scopus

    SLC33A1 mutation (Huppke-Brendel Syndrome) is a rare, autosomal recessive disorder associated with copper metabolism and characterized by global developmental delay, sensorineural hearing loss, congenital cataract and generalized hypotonia. We report two siblings under 6 years with novel SLC33A1…

  9. Artikel Jurnal

    Status epilepticus as a novel etiology of Lance–Adams syndrome: a case report

    Fuli Wang; Lei Xu; Ting Huang dkk.

    Epilepsy & Behavior Reports, Vol. 36 · 2026 · Inggris · DOAJ Scopus

    Lance–Adams syndrome (LAS) is a rare neurological disorder characterized by action myoclonus. The majority of reported cases have occurred following resuscitation from cardiopulmonary arrest, and to our knowledge, no previous case has been documented in the setting of status epilepticus. In this…

  10. Artikel Jurnal

    Financial and clinical impact of clinical pharmacist practitioner-led follow-up in a VA epilepsy clinic

    Dragana Vlaski; Barry Gidal; Katherine Rotzenberg dkk.

    Epilepsy & Behavior Reports, Vol. 36 · 2026 · Inggris · DOAJ Scopus

    Background: Epilepsy is a chronic neurologic condition that requires specialist follow-up and frequent medication adjustments. A multidisciplinary Veterans Affairs (VA) clinic model was implemented in which clinical pharmacist practitioners (CPPs) provide follow-up care under epileptologist…

  11. Artikel Jurnal

    Fenfluramine for seizures in Dravet syndrome and Lennox-Gastaut syndrome: Mechanisms, clinical evidence, safety, and practical integration

    József Janszky; József Janszky, Jr; Réka Horváth

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Developmental and epileptic encephalopathies such as Dravet syndrome and Lennox–Gastaut syndrome remain highly drug resistant and are associated with substantial neurodevelopmental, behavioral, and caregiver burdens. Fenfluramine, repurposed at low antiseizure doses, is approved as adjunctive…

  12. Artikel Jurnal

    Lived experiences of young people with epilepsy in a resource-constraint setting: Contemporary findings from Cape Coast, Ghana

    Akwasi Appiah; Kwasi Agyen-Mensah; Akua Afriyie Karikari dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Epilepsy is a chronic neurological condition that affects millions of young people globally, often leading to physical, cognitive, psychological, and social challenges. In resource-constraint settings, access to healthcare and medications, stigma, and psychosocial burdens can further exacerbate the…

  13. Artikel Jurnal

    Chorea–athetosis-like hyperkinetic seizures in temporal lobe epilepsy: insights from stereo-EEG in three patients

    Jun Zhuang; Lingxia Fei; Hua Li dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Purpose: To characterize the clinical and electrographic features of temporal lobe epilepsy (TLE) presenting with chorea–athetosis-like hyperkinetic seizures and to delineate the underlying seizure network using stereo-electroencephalography (SEEG). Methods: We retrospectively reviewed 102…

  14. Artikel Jurnal

    Seizure freedom after vagus nerve stimulation in a patient with

    Victoria Esmeralda Juárez-Rivera; Juan Carlos Vera-López; Diana Trinidad-Hernández dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Genetic-based epilepsies often present as distributed neural network disorders, challenging traditional focal versus generalized classifications. We report a 20-year-old male with drug-resistant epilepsy associated with a previously unreported SCN3A missense variant (c.5970C > G; p.Ser1990Arg)…

  15. Artikel Jurnal

    Comparative trends in idiopathic epilepsy burden in China and worldwide based on Global Burden of Disease Study 2021

    Xueshi Tian; Yu Geng; Xiang Chen dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Background: Idiopathic epilepsy, defined by the absence of identifiable structural or metabolic etiologies, remains a significant contributor to the global neurological disease burden. However, long-term comparisons between China and the global level are limited. This study analyzed and compared…

  16. Artikel Jurnal

    Comparison of selective amygdalohippocampectomy and anterior temporal lobectomy for mesial temporal lobe epilepsy: a systematic review and meta-analysis

    Vinícius Barone; Paulo Henrique Pires de Aguiar

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Background: Anterior temporal lobectomy (ATL) and selective amygdalohippocampectomy (SAH) are the two most widely adopted surgical approaches for drug-resistant mesial temporal lobe epilepsy (MTLE). Although both procedures target seizure control, they differ in extent of resection and potential…

  17. Artikel Jurnal

    Everolimus initiated in the neonatal period for refractory seizures associated with tuberous sclerosis complex: long-term clinical outcome

    Yoong-A Suh; Seong Wan Kim; Seohui Choi dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Objective: Everolimus is an established therapy for tumor manifestations and refractory focal seizures in tuberous sclerosis complex (TSC) in patients aged ≥2 years. Evidence regarding its use during the neonatal period, particularly for seizure control, remains extremely limited. Methods: We…

  18. Artikel Jurnal

    The electroclinical phenotype of epilepsy following autoimmune encephalitis

    Stephan Neidhart; Tena Dubcek; Debora Ledergerber dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Objective: To describe the temporal and spatial dynamics of electroencephalographic (EEG) recordings in epilepsy following autoimmune encephalitis (AE) compared to temporal lobe epilepsy (TLE) without signs of inflammatory etiology. Methods: We assessed electroencephalographic properties using…

  19. Artikel Jurnal

    Expanding the phenotypic Spectrum of ZNF711: Autism and epilepsy in two siblings

    Gloria Urciuoli; Nicola Simeone; Marica Rubino dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Zinc Finger Protein 711 (ZNF711) is a Krüppel-type zinc finger transcription factor highly expressed in the brain and whose mutations have been associated with neurodevelopmental disorders such as intellectual disability, autism spectrum disorder, and epilepsy. While most pathogenic variants…

  20. Artikel Jurnal

    Lived experiences that influence the quality of life among patients with epilepsy at Mulago National Referral Hospital

    Humphrey Atwijukiire; Juliana Namutundu; David Lubogo dkk.

    Epilepsy & Behavior Reports, Vol. 35 · 2026 · Inggris · DOAJ Scopus

    Background: In Uganda, the quality of life (QoL) of patients with epilepsy (PWE) remains poor due to clinical, psychological, and social challenges. While several quantitative studies have documented correlates of poor QoL in Ugandan PWE, the specific mechanisms, contextual meanings, and…