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Correlation between autistic traits and brain functional connectivity in preschoolers with autism spectrum disorder: a resting state MEG study.
- Published in:
- Neurological Sciences, 2024, v. 45, n. 9, p. 4549, doi. 10.1007/s10072-024-07528-2
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- Article
Antidepressant effect of vagal nerve stimulation in epilepsy patients: a systematic review.
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- 2020
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- Publication type:
- journal article
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results.
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- 2019
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- Publication type:
- journal article
Death in Unverricht-Lundborg disease.
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- 2009
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- Publication type:
- journal article
Death in Unverricht–Lundborg disease.
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- Neurological Sciences, 2009, v. 30, n. 4, p. 315, doi. 10.1007/s10072-009-0102-2
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- Publication type:
- Article
Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age.
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- Journal of Child Neurology, 2015, v. 30, n. 13, p. 1824, doi. 10.1177/0883073815583687
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- Article
Comparison of Resampling Techniques for Imbalanced Datasets in Machine Learning: Application to Epileptogenic Zone Localization From Interictal Intracranial EEG Recordings in Patients With Focal Epilepsy.
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- Frontiers in Neuroinformatics, 2021, v. 15, p. 1, doi. 10.3389/fninf.2021.715421
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- Publication type:
- Article
EEG-informed fMRI analysis during a hand grip task: estimating the relationship between EEG rhythms and the BOLD signal.
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- Frontiers in Human Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fnhum.2014.00186
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- Publication type:
- Article
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
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- 2022
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- Publication type:
- journal article
Early-onset phenotype of bi-allelic GRN mutations.
- Published in:
- 2021
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- Publication type:
- Letter
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 4, p. e40, doi. 10.1111/epi.12944
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- Article
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings.
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- Epilepsia (Series 4), 2014, v. 55, n. 12, p. e129, doi. 10.1111/epi.12806
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- Publication type:
- Article
Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation.
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- Epilepsia (Series 4), 2014, v. 55, n. 6, p. e56, doi. 10.1111/epi.12632
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- Publication type:
- Article
Theory of mind and epilepsy: What clinical implications?
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- Epilepsia (Series 4), 2013, v. 54, n. 9, p. 1639, doi. 10.1111/epi.12255
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- Publication type:
- Article
Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndrome.
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- Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1251, doi. 10.1111/epi.12213
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- Publication type:
- Article
Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.
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- Epilepsia (Series 4), 2013, v. 54, n. 5, p. 927, doi. 10.1111/epi.12123
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- Publication type:
- Article
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2120, doi. 10.1111/j.1528-1167.2012.03718.x
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- Publication type:
- Article
Focal epilepsies in adult patients attending two epilepsy centers: Classification of drug-resistance, assessment of risk factors, and usefulness of 'new' antiepileptic drugs.
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- Epilepsia (Series 4), 2012, v. 53, n. 4, p. 733, doi. 10.1111/j.1528-1167.2012.03416.x
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- Publication type:
- Article
Enhanced frontocentral EEG connectivity in photosensitive generalized epilepsies: A partial directed coherence study.
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- Epilepsia (Series 4), 2012, v. 53, n. 2, p. 359, doi. 10.1111/j.1528-1167.2011.03352.x
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- Publication type:
- Article
Pure haploinsufficiency for Dravet syndrome Na<sub>V</sub>1.1 ( SCN1A) sodium channel truncating mutations.
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- Epilepsia (Series 4), 2012, v. 53, n. 1, p. 87, doi. 10.1111/j.1528-1167.2011.03346.x
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- Publication type:
- Article
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.
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- Epilepsia (Series 4), 2011, v. 52, n. 12, p. 2356, doi. 10.1111/j.1528-1167.2011.03307.x
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- Publication type:
- Article
Theory of mind in frontal and temporal lobe epilepsy: Cognitive and neural aspects.
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- Epilepsia (Series 4), 2011, v. 52, n. 11, p. 1995, doi. 10.1111/j.1528-1167.2011.03215.x
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- Publication type:
- Article
ICTAL EEG Fast Activity in West Syndrome: From Onset to Outcome.
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- Epilepsia (Series 4), 2007, v. 48, n. 11, p. 2101, doi. 10.1111/j.1528-1167.2007.01264.x
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- Publication type:
- Article
Electroclinical Features of a Family with Simple Febrile Seizures and Temporal Lobe Epilepsy Associated with SCN1A Loss-of-Function Mutation.
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- Epilepsia (Series 4), 2007, v. 48, n. 9, p. 1691, doi. 10.1111/j.1528-1167.2007.01153.x
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- Publication type:
- Article
Epileptogenic Channelopathies: Experimental Models of Human Pathologies.
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- Epilepsia (Series 4), 2007, v. 48, p. 51, doi. 10.1111/j.1528-1167.2007.01067.x
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- Publication type:
- Article
Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease.
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- Epilepsia (Series 4), 2006, v. 47, n. 3, p. 640, doi. 10.1111/j.1528-1167.2006.00479.x
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- Publication type:
- Article
Periventricular Nodular Heterotopia: Classification, Epileptic History, and Genesis of Epileptic Discharges.
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- Epilepsia (Series 4), 2006, v. 47, n. 1, p. 86, doi. 10.1111/j.1528-1167.2006.00374.x
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- Publication type:
- Article
Functional MRI in Malformations of Cortical Development: Activation of Dysplastic Tissue and Functional Reorganization.
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- Journal of Neuroimaging, 2008, v. 18, n. 3, p. 296, doi. 10.1111/j.1552-6569.2007.00164.x
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- Publication type:
- Article
Predicting Functional Recovery in Chronic Stroke Rehabilitation Using Event-Related Desynchronization-Synchronization during Robot-Assisted Movement.
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- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/7051340
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- Publication type:
- Article
Early cortico-muscular coherence and cortical network changes in Parkinson's patients treated with MRgFUS.
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- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1362712
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- Publication type:
- Article
Anatomically compliant modes of variations: New tools for brain connectivity.
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- PLoS ONE, 2023, v. 18, n. 11, p. 1, doi. 10.1371/journal.pone.0292450
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- Publication type:
- Article
Seizures and EEG features in 74 patients with genetic-dysmorphic syndromes.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 12, p. 3154, doi. 10.1002/ajmg.a.36746
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- Publication type:
- Article
Analyzing the Loss and the Recovery of Consciousness: Functional Connectivity Patterns and Changes in Heart Rate Variability During Propofol-Induced Anesthesia.
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- Frontiers in Systems Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnsys.2021.652080
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- Publication type:
- Article
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability.
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- Frontiers in Molecular Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnmol.2018.00269
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- Publication type:
- Article
Simultaneous EEG-fMRI in Patients with Unverricht-Lundborg Disease: Event-Related Desynchronization/Synchronization and Hemodynamic Response Analysis.
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- Computational Intelligence & Neuroscience, 2010, p. 1, doi. 10.1155/2010/164278
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- Publication type:
- Article
Is Period3 Genotype Associated With Sleep and Recovery in Patients With Disorders of Consciousness?
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- Neurorehabilitation & Neural Repair, 2016, v. 30, n. 5, p. 461, doi. 10.1177/1545968315604398
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- Publication type:
- Article
Phenytoin Inhibits the Persistent Sodium Current in Neocortical Neurons by Modifying Its Inactivation Properties.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055329
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- Publication type:
- Article
Paroxysmal non-epileptic motor events in childhood: a clinical and video-EEG-polymyographic study.
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- Developmental Medicine & Child Neurology, 2012, v. 54, n. 4, p. 334, doi. 10.1111/j.1469-8749.2011.04217.x
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- Publication type:
- Article
Entropy Metrics Correlating with Higher Residual Functioning in Patients with Chronic Disorders of Consciousness.
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- Brain Sciences (2076-3425), 2022, v. 12, n. 3, p. 332, doi. 10.3390/brainsci12030332
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- Publication type:
- Article
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12671-y
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- Publication type:
- Article
Towards the Automatic Localization of the Irritative Zone Through Magnetic Source Imaging.
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- Brain Topography, 2020, v. 33, n. 5, p. 651, doi. 10.1007/s10548-020-00789-y
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- Publication type:
- Article
Cerebellar Involvement in Patients with Mild to Moderate Myoclonus Due to EPM1: Structural and Functional MRI Findings in Comparison with Healthy Controls and Ataxic Patients.
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- Brain Topography, 2017, v. 30, n. 3, p. 380, doi. 10.1007/s10548-016-0534-y
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- Publication type:
- Article
Neural Signatures of Economic Parameters During Decision-Making: A Functional MRI (fMRI), Electroencephalography (EEG) and Autonomic Monitoring Study.
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- Brain Topography, 2012, v. 25, n. 1, p. 73, doi. 10.1007/s10548-011-0210-1
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- Publication type:
- Article
Self-Limited Hyperexcitability: Functional Effect of a Familial Hemiplegic Migraine Mutation of the Na<sub>v</sub>1.1 (SCN1A) Na<sup>+</sup> Channel.
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- Journal of Neuroscience, 2008, v. 28, n. 29, p. 7273, doi. 10.1523/JNEUROSCI.4453-07.2008
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- Publication type:
- Article
Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Na<sub>v</sub>1.1<sup>+</sup> Na Channel Mutant.
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- Journal of Neuroscience, 2007, v. 27, n. 41, p. 11037, doi. 10.1523/JNEUROSCI.3515-07.2007
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- Publication type:
- Article
Effects in Neocortical Neurons of Mutations of the Nav1.2 Na<sup>+</sup> Channel causing Benign Familial Neonatal-Infantile Seizures.
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- Journal of Neuroscience, 2006, v. 26, n. 40, p. 10100, doi. 10.1523/JNEUROSCI.2476-06.2006
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- Publication type:
- Article
Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach.
- Published in:
- Epilepsia Open, 2024, v. 9, n. 5, p. 1922, doi. 10.1002/epi4.13039
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- Publication type:
- Article
Myoclonus: Differential diagnosis and current management.
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- Epilepsia Open, 2024, v. 9, n. 2, p. 486, doi. 10.1002/epi4.12917
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- Publication type:
- Article
Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes.
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- Epilepsia Open, 2023, v. 8, n. 2, p. 645, doi. 10.1002/epi4.12697
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- Publication type:
- Article
IRF2BPL: A new genotype for progressive myoclonus epilepsies.
- Published in:
- Epilepsia (Series 4), 2023, v. 64, n. 8, p. e164, doi. 10.1111/epi.17557
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- Publication type:
- Article