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| 37950390 | Long-term treatment with ganaxolone for seizures associated with cyclin-dependent kinase-like 5 deficiency disorder: Two-year open-label extension follow-up. | Epilepsia | 2024 |
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| 37745363 | Timing and location of speech errors induced by direct cortical stimulation. | bioRxiv | 2024 |
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| 37882730 | Cannabinoid treatments in epilepsy and seizure disorders. | Physiol Rev | 2024 |
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| 37758268 | Association between changes in carbohydrate intake and long term weight changes: prospective cohort study. | BMJ | 2023 |
| 37521285 | Localized proteomic differences in the choroid plexus of Alzheimer's disease and epilepsy patients. | Front Neurol | 2023 |
| 37658852 | Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein. | Genet Med | 2023 |
| 37745380 | A Neural Speech Decoding Framework Leveraging Deep Learning and Speech Synthesis. | bioRxiv | 2023 |
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| 37425747 | A shared linguistic space for transmitting our thoughts from brain to brain in natural conversations. | bioRxiv | 2023 |
| 37316509 | The role of superficial and deep layers in the generation of high frequency oscillations and interictal epileptiform discharges in the human cortex. | Sci Rep | 2023 |
| 37150937 | Flexible, high-resolution cortical arrays with large coverage capture microscale high-frequency oscillations in patients with epilepsy. | Epilepsia | 2023 |
| 37343704 | Comparing measured dietary variation within and between tropical hunter-gatherer groups to the Paleo Diet. | Am J Clin Nutr | 2023 |
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| 37407557 | Closed-loop brain stimulation augments fear extinction in male rats. | Nat Commun | 2023 |
| 37308910 | Expanding genotype-phenotype correlations in FOXG1 syndrome: results from a patient registry. | Orphanet J Rare Dis | 2023 |
| 37075751 | POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies. | Am J Hum Genet | 2023 |
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| 36994379 | Ictal ECG-based assessment of sudden unexpected death in epilepsy. | Front Neurol | 2023 |
| 36855241 | Failure to use new breakthrough treatments for epilepsy. | Epilepsia | 2023 |
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| 36648376 | Risk of sudden unexpected death in epilepsy (SUDEP) with lamotrigine and other sodium channel-modulating antiseizure medications. | Epilepsia Open | 2023 |
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| 36686527 | Autonomic dysfunction in epilepsy mouse models with implications for SUDEP research. | Front Neurol | 2023 |
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| 36539302 | Mood and Anxiety Disorders and Suicidality in Patients With Newly Diagnosed Focal Epilepsy: An Analysis of a Complex Comorbidity. | Neurology | 2023 |
| 36775798 | Metabolomic, proteomic, and transcriptomic changes in adults with epilepsy on modified Atkins diet. | Epilepsia | 2023 |
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| 36865223 | Precise Spatial Tuning of Visually Driven Alpha Oscillations in Human Visual Cortex. | bioRxiv | 2023 |
| 36336987 | Brain molecular mechanisms in Rasmussen encephalitis. | Epilepsia | 2023 |
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| 35587487 | Pilot study evaluating everolimus molecular mechanisms in tuberous sclerosis complex and focal cortical dysplasia. | PLoS One | 2022 |
| 35478467 | Serotonin transporter in the temporal lobe, hippocampus and amygdala in SUDEP. | Brain Pathol | 2022 |
| 35370908 | Interictal EEG and ECG for SUDEP Risk Assessment: A Retrospective Multicenter Cohort Study. | Front Neurol | 2022 |
| 35833929 | Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein. | Genet Med | 2022 |
| 35463127 | Remote Memory in Epilepsy: Assessment, Impairment, and Implications Regarding Hippocampal Function. | Front Neurol | 2022 |
| 35395208 | Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome. | Am J Hum Genet | 2022 |
| 35663384 | Intraoperative microseizure detection using a high-density micro-electrocorticography electrode array. | Brain Commun | 2022 |
| 35528136 | Religious conversion in an older male with longstanding epilepsy. | Epilepsy Behav Rep | 2022 |
| 35691218 | Genomics in the presurgical epilepsy evaluation. | Epilepsy Res | 2022 |
| 35780567 | KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism. | EBioMedicine | 2022 |
| 37215328 | The Precentral Gyrus Contributions to the Early Time-Course of Grapheme-to-Phoneme Conversion. | Neurobiol Lang (Camb) | 2022 |
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