Found: 36
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Mismatch Negativity Recording in Children With Duchenne Muscular Dystrophy.
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- Journal of Child Neurology, 2016, v. 31, n. 13, p. 1468, doi. 10.1177/0883073816656404
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- Publication type:
- Article
Guideline recommendations for diagnosis and clinical management of Ring14 syndrome-first report of an ad hoc task force.
- Published in:
- 2017
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- Publication type:
- journal article
Comparing cortical auditory processing in children with typical and atypical benign epilepsy with centrotemporal spikes: Electrophysiologic evidence of the role of non-rapid eye movement sleep abnormalities.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 5, p. 726, doi. 10.1111/epi.12959
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- Publication type:
- Article
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.
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- Epilepsia (Series 4), 2015, v. 56, n. 5, p. 692, doi. 10.1111/epi.12977
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- Publication type:
- Article
Epilepsy in ring 14 syndrome: A clinical and EEG study of 22 patients.
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- Epilepsia (Series 4), 2013, v. 54, n. 12, p. 2204, doi. 10.1111/epi.12393
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- Publication type:
- Article
Neuropsychological approaches to epileptic encephalopathies.
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- Epilepsia (Series 4), 2013, v. 54, p. 38, doi. 10.1111/epi.12422
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- Publication type:
- Article
Epilepsy and vaccinations: Italian guidelines.
- Published in:
- Epilepsia (Series 4), 2013, v. 54, p. 13, doi. 10.1111/epi.12306
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- Publication type:
- Article
Clinical dissection of early onset absence epilepsy in children and prognostic implications.
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- Epilepsia (Series 4), 2013, v. 54, n. 10, p. 1761, doi. 10.1111/epi.12341
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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
Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations.
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- Epilepsia (Series 4), 2007, v. 48, n. 6, p. 1092, doi. 10.1111/j.1528-1167.2007.01020.x
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- Publication type:
- Article
Diagnosis and Treatment of the First Epileptic Seizure: Guidelines of the Italian League Against Epilepsy.
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- Epilepsia (Series 4), 2006, v. 47, p. 2, doi. 10.1111/j.1528-1167.2006.00869.x
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- Publication type:
- Article
Neuropsychological Findings: Myoclonic Astatic Epilepsy (MAE) and Lennox-Gastaut Syndrome (LGS).
- Published in:
- Epilepsia (Series 4), 2006, v. 47, p. 56, doi. 10.1111/j.1528-1167.2006.00691.x
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- Publication type:
- Article
The Spectrum of Idiopathic Rolandic Epilepsy Syndromes and Idiopathic Occipital Epilepsies: From the Benign to the Disabling.
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- Epilepsia (Series 4), 2006, v. 47, p. 62, doi. 10.1111/j.1528-1167.2006.00693.x
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- Publication type:
- Article
Idiopathic Generalized Epilepsies of Adolescence.
- Published in:
- Epilepsia (Series 4), 2006, v. 47, p. 107, doi. 10.1111/j.1528-1167.2006.00706.x
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- Publication type:
- Article
Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations.
- Published in:
- Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1629, doi. 10.1111/j.1528-1167.2006.00641.x
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- Publication type:
- Article
Short-term Nonhormonal and Nonsteroid Treatment in West Syndrome.
- Published in:
- 2004
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- Correction Notice
Short-term Nonhormonal and Nonsteroid Treatment in West Syndrome.
- Published in:
- Epilepsia (Series 4), 2003, v. 44, n. 8, p. 1085, doi. 10.1046/j.1528-1157.2003.55402.x
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- Publication type:
- Article
Lack of SCN1A Mutations in Familial Febrile Seizures.
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- Epilepsia (Series 4), 2002, v. 43, n. 5, p. 559, doi. 10.1046/j.1528-1157.2002.29301.x
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- Publication type:
- Article
Learning Disability in Epilepsy: Definitions and Classification.
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- Epilepsia (Series 4), 2001, v. 42, p. 2, doi. 10.1046/j.1528-1157.2001.042004575.x
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- Publication type:
- Article
'Minimal' holoprosencephaly in a 14q deletion syndrome patient.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 12, p. 3216, doi. 10.1002/ajmg.a.38378
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- Publication type:
- Article
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
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- Nature Genetics, 2014, v. 46, n. 6, p. 640, doi. 10.1038/ng.2952
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- Publication type:
- Article
Oxidative Stress and Erythrocyte Membrane Alterations in Children with Autism: Correlation with Clinical Features.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066418
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- Publication type:
- Article
Psychogenic Non-Epileptic Seizures: A Diagnostic Problem Difficult to Solve in Clinical Practice.
- Published in:
- Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2012, v. 49, n. 4, p. 243, doi. 10.4274/npa.y6687
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- Publication type:
- Article
Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults.
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- Brain: A Journal of Neurology, 2010, v. 133, n. 12, p. 3598
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- Publication type:
- Article
Periodic spasms: an unclassified type of epileptic seizure in childhood.
- Published in:
- 1987
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- Publication type:
- journal article
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.
- Published in:
- Epilepsia (Series 4), 2024, v. 65, n. 3, p. 779, doi. 10.1111/epi.17859
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- Publication type:
- Article
Chromosome 14 deletions, rings, and epilepsy genes: A riddle wrapped in a mystery inside an enigma.
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- Epilepsia (Series 4), 2021, v. 62, n. 1, p. 25, doi. 10.1111/epi.16754
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- Publication type:
- Article
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generation.
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- Epilepsia (Series 4), 2016, v. 57, n. 6, p. 896, doi. 10.1111/epi.13385
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- Publication type:
- Article
Brivaracetam in treating epileptic encephalopathy and refractory focal epilepsies in patients under 14 years of age.
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- Iranian Journal of Child Neurology, 2021, v. 15, n. 4, p. 95, doi. 10.22037/ijcn.v15i4.29819
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- Publication type:
- Article
Corticosteroids versus clobazam in epileptic encephalopathy with ESES: a European multicentre randomised controlled clinical trial (RESCUE ESES*).
- Published in:
- 2020
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- Publication type:
- journal article
A reflection on the role of genetics in the concept of "epileptic encephalopathy", as emerged from the most recent ILEA classification of epilepsy.
- Published in:
- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. 1, doi. 10.1186/s13052-019-0765-0
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- Publication type:
- Article
Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal Spikes.
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- Frontiers in Neurology, 2019, v. 10, p. 1, doi. 10.3389/fneur.2019.01316
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- Publication type:
- Article
Lack of SLC2A1 (Glucose Transporter 1) Mutations in 30 Italian Patients With Alternating Hemiplegia of Childhood.
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- Journal of Child Neurology, 2013, v. 28, n. 7, p. 863, doi. 10.1177/0883073812452789
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- Publication type:
- Article
Seizure and EEG Patterns in Angelman's Syndrome.
- Published in:
- Journal of Child Neurology, 1995, v. 10, n. 6, p. 467, doi. 10.1177/088307389501000609
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- Publication type:
- Article
Self-Induced Stretch Syncope: An Unusual Non-Epileptic Paroxysmal Event. A Case Report and Literature Mini-Review.
- Published in:
- Clinical Medicine Insights: Pediatrics, 2024, p. 1, doi. 10.1177/11795565241249596
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- Publication type:
- Article
Clinical heterogeneity of adhalin deficiency.
- Published in:
- 1996
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- Publication type:
- journal article