Found: 24
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Prognostic role of Mini-Mental State Pediatric Examination (MMSPE) on neuropsychological functioning.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Children With Convulsive Epileptic Seizures Presenting to Padua Pediatric Emergency Department: The First Retrospective Population-Based Descriptive Study in an Italian Health District.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 3, p. 289, doi. 10.1177/0883073814538670
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- Publication type:
- Article
Longitudinal Electroencephalographic (EEG) Findings in Pediatric Anti-N-Methyl-d-Aspartate (Anti-NMDA) Receptor Encephalitis: The Padua Experience.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 2, p. 238, doi. 10.1177/0883073813515947
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- Publication type:
- Article
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
- Published in:
- Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1288, doi. 10.1111/epi.12194
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- Publication type:
- Article
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy.
- Published in:
- Epilepsia (Series 4), 2011, v. 52, n. 4, p. 802, doi. 10.1111/j.1528-1167.2010.02976.x
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- Publication type:
- Article
Executive Functions and Attention in Childhood Epilepsies: A Neuropsychological Hallmark of Dysfunction?
- Published in:
- Journal of the International Neuropsychological Society, 2021, v. 27, n. 7, p. 673, doi. 10.1017/S1355617720001125
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- Publication type:
- Article
First-ever convulsive seizures in children presenting to the emergency department: risk factors for seizure recurrence and diagnosis of epilepsy.
- Published in:
- 2019
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- Publication type:
- journal article
Non-convulsive status epilepticus of frontal origin in mucopolysaccharidosis type II successfully treated with ethosuximide.
- Published in:
- Developmental Medicine & Child Neurology, 2012, v. 54, n. 10, p. 961, doi. 10.1111/j.1469-8749.2012.04228.x
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- Publication type:
- Article
Identification of Four Novel PCDH19 Mutations and Prediction of Their Functional Impact.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 6, p. 389, doi. 10.1111/ahg.12082
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- Publication type:
- Article
Gain of function SCN1A disease‐causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication.
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- Epilepsia (Series 4), 2023, v. 64, n. 5, p. 1331, doi. 10.1111/epi.17509
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- Publication type:
- Article
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 11, p. 1808, doi. 10.1111/epi.13574
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- Publication type:
- Article
Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?
- Published in:
- Journal of Headache & Pain, 2011, v. 12, n. 4, p. 435, doi. 10.1007/s10194-011-0359-8
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- Publication type:
- Article
Comorbidity between headache and epilepsy in a pediatric headache center.
- Published in:
- Journal of Headache & Pain, 2010, v. 11, n. 3, p. 235, doi. 10.1007/s10194-010-0191-6
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- Publication type:
- Article
Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy.
- Published in:
- 2018
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- Publication type:
- journal article
Identification of SETBP1 Mutations by Gene Panel Sequencing in Individuals With Intellectual Disability or With "Developmental and Epileptic Encephalopathy".
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.593446
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- Publication type:
- Article
Dexmedetomidine for EEG sedation in children with behavioral disorders.
- Published in:
- Acta Neurologica Scandinavica, 2020, v. 142, n. 5, p. 493, doi. 10.1111/ane.13293
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- Publication type:
- Article
Clues for Minimal Hepatic Encephalopathy in Children With Noncirrhotic Portal Hypertension.
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- Journal of Pediatric Gastroenterology & Nutrition, 2014, v. 59, n. 6, p. 689, doi. 10.1097/MPG.0000000000000537
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- Publication type:
- Article
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy.
- Published in:
- Epilepsy Research & Treatment, 2011, p. 1, doi. 10.1155/2011/258365
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- Publication type:
- Article
Pathogenic Role of the X-Linked Cyclin-Dependent Kinase-Like 5 and Aristaless-Related Homeobox Genes in Epileptic Encephalopathy of Unknown Etiology With Onset in the First Year of Life.
- Published in:
- Journal of Child Neurology, 2011, v. 26, n. 6, p. 683, doi. 10.1177/0883073810387827
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- Publication type:
- Article
Bilateral Perysilvian Polymicrogyria With Cerebellar Dysplasia and Ectopic Neurohypophysis.
- Published in:
- Journal of Child Neurology, 2011, v. 26, n. 3, p. 361, doi. 10.1177/0883073810381447
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- Publication type:
- Article
Pre- and Postprandial Electroencephalography in Glucose Transporter Type 1 Deficiency Syndrome: An Illustrative Case to Discuss the Concept of Carbohydrate Responsiveness.
- Published in:
- Journal of Child Neurology, 2011, v. 26, n. 1, p. 103, doi. 10.1177/0883073810376444
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- Publication type:
- Article
Efficacy and Safety of Topiramate in Refractory Epilepsy of Childhood: Long-Term Follow-Up Study.
- Published in:
- Journal of Child Neurology, 2005, v. 20, n. 11, p. 893, doi. 10.1177/08830738050200110601
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- Publication type:
- Article
A Novel WAC Loss of Function Mutation in an Individual Presenting with Encephalopathy Related to Status Epilepticus during Sleep (ESES).
- Published in:
- Genes, 2020, v. 11, n. 3, p. 344, doi. 10.3390/genes11030344
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- Publication type:
- Article
Benign nocturnal alternating hemiplegia of childhood: The first clinical report with paroxysmal events home-video recordings.
- Published in:
- Movement Disorders, 2008, v. 23, n. 11, p. 1605, doi. 10.1002/mds.22180
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- Publication type:
- Article