Ann Neurol

1. ROUTLEDGE N, Lammens M, Maroofian R, Beland B, et al
   Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit beta3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia.
   Ann Neurol. 2025 Aug 23. doi: 10.1002/ana.78014.
   

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2. BROOKER SM, Novelli M, Coukos R, Prakash N, et al
   The Spectrum of Neurologic Phenotypes Associated With NUS1 Pathogenic Variants: A Comprehensive Case Series.
   Ann Neurol. 2025;98:561-572.
   

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3. ABDALLAH C, Thomas J, Aron O, Avigdor T, et al
   Visual Features in Stereo-Electroencephalography to Predict Surgical Outcome: A Multicenter Study.
   Ann Neurol. 2025;98:547-560.
   

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   BMC Neurol

4. NATARAJAN J, Joseph MA, Al-Asmi A, Seshan V, et al
   Quality of life, depression, daytime sleepiness and fatigue in Omani people with epilepsy: a cross-sectional study.
   BMC Neurol. 2025;25:366.
   

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   Brain Res

5. IVLEV AP, Filippova RA, Aleksandrova EP, Kulikov AA, et al
   Alterations of GABAergic transmission in the hippocampus of aging Krushinsky-Molodkina rats genetically prone to audiogenic seizures.
   Brain Res. 2025;1863:149847.
   

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   Epilepsia

6. BAYKAN B, Dunne J, Wiebe S, Maillard L, et al
   Presence of interictal epileptiform EEG discharges implies increased risk of recurrence after the first unprovoked seizure: Report of the International League Against Epilepsy and International Federation of Clinical Neurophysiology.
   Epilepsia. 2025 Aug 28. doi: 10.1111/epi.18591.
   

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7. SZAFLARSKI JP, Nenert R, Hong H, Mueller C, et al
   Exploratory study of peripheral immune changes associated with diffusion MRI multi-compartment model in temporal lobe epilepsy.
   Epilepsia. 2025 Aug 28. doi: 10.1111/epi.18612.
   

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   Epilepsy Res

8. VASILICA AM, Dhaliwal JK, Dasgupta D, Chari A, et al
   Outcomes of surgically and non-surgically managed temporal encephalocoeles in the context of drug-resistant temporal lobe epilepsy: A retrospective single-centre case series.
   Epilepsy Res. 2025;218:107643.
   

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9. RHODES C, Rees B, Dubbs H, Lesser M, et al
   Natural history of epilepsy in FOXG1 Syndrome.
   Epilepsy Res. 2025;218:107644.
   

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   J Child Neurol

10. BDAIR M, Hajjeh O, Takhman M, Abukhalil MM, et al
    Developmental Epileptic Encephalopathy in a Pediatric Patient: Insights from a Novel SULT4A1 Variant and Genetic Challenges.
    J Child Neurol. 2025 Aug 29:8830738251369139. doi: 10.1177/08830738251369139.
    

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    Neurology

11. TRIVISANO M, Specchio N
    The Role of Caregiver Surveys in Clinical Research of Developmental and Epileptic Encephalopathies.
    Neurology. 2025;105:e214056.
    

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12. GAO K, Riley LG, Raubenheimer J, Oliver KL, et al
    WWOX-Related Developmental and Epileptic Encephalopathy: Expanding the Clinical Spectrum and Deciphering the Genotype-Phenotype.
    Neurology. 2025;105:e213883.
    

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13. GOTLIEB E, Lally A, Blank LJ, Jette N, et al
    Geographic Heterogeneity in Epilepsy Specialist Distribution.
    Neurology. 2025;105:e214035.
    

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    PLoS Genet

14. EL GHALEB Y, Fernandez-Quintero ML, Campiglio M, Tuluc P, et al
    Two pairs of CACNA1I (CaV3.3) variants with opposite effects on channel function cause neurodevelopmental disorders of varying severity.
    PLoS Genet. 2025;21:e1011828.
    

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    Seizure

15. EZZI S, Salamatullah HK, Alzahrani D, Alshrif A, et al
    Effectiveness and safety of midazolam versus lorazepam for pediatric status epilepticus: A systematic review and meta-analysis.
    Seizure. 2025;132:4-12.
    

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16. RAMOS AJ, Lazarowski A, Vega-Garcia A, Buritica-Ramirez E, et al
    Modulation of neuroinflammation as a therapeutic strategy for the control of epilepsy.
    Seizure. 2025;131:458-470.
    

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17. KRENN M, Nenning KH, Aull-Watschinger S, Pataraia E, et al
    ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsy.
    Seizure. 2025;131:454-457.
    

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