ReviewItalian journal of pediatrics2018
Benign and severe early-life seizures: a round in the first year of life.
Review in Italian journal of pediatrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
16 citing papers in PubMed, 39 citations in OpenAlex.
- An interpretable machine learning model for predicting febrile seizures following enterovirus infection in children.Annals of medicine · 2026Article
- Study of Clinico-Etiological Profile of New-Onset Seizure in Infants.Journal of pharmacy & bioallied sciences · 2025Article
- Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature.Epileptic disorders : international epilepsy journal with videotape · 2025Review
- Trends in Prevalence and Incidence of Epilepsy and Drug-Resistant Epilepsy in Children: A Nationwide Population-Based Study in Korea.Neurology international · 2024Article
- Best practices for the management of febrile seizures in children.Italian journal of pediatrics · 2024Review
- Awareness of Nigerian Mothers on the Risk Factors, Prevention and Management of Seizures in Newborns.Iranian journal of child neurology · 2023Article
- Etiological and risk factors in recurrent febrile seizures: Insights through EEG analysis.Qatar medical journal · 2023Article
- Mouse models of Kcnq2 dysfunction.Epilepsia · 2022Review
- Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions.Frontiers in pediatrics · 2022Review
- The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy.Scientific reports · 2021Article
- Benign juvenile idiopathic epilepsy in captive Iberian lynx (Lynx pardinus) in the ex situ conservation program (2005-2019).BMC veterinary research · 2021Article
- Over 10-Year Outcomes of Infantile-Onset Epilepsies.Journal of clinical medicine · 2021Article
- Article
- PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?Italian journal of pediatrics · 2019Review
- Report on advances for pediatricians in 2018: allergy, cardiology, critical care, endocrinology, hereditary metabolic diseases, gastroenterology, infectious diseases, neonatology, nutrition, respiratory tract disorders and surgery.Italian journal of pediatrics · 2019Review
- A Child with a c.6923_6928dup (p.Arg2308_Met2309dup)International journal of molecular sciences · 2018Article
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAt the onset, differentiation between abnormal non-epileptic movements, and epileptic seizures presenting in early life is difficult as is clinical diagnosis and prognostic evaluation of the various seizure disorders presenting at this age. Seizures starting in the first year of life including the neonatal period might have a favorable course, such as in infants presenting with benign familial neonatal epilepsy, febrile seizures simplex or acute symptomatic seizures. However, in some cases, the onset of seizures at birth or in the first months of life have a dramatic evolution with severe cerebral impairment. Seizure disorders starting in early life include the "epileptic encephalopathies", a group of conditions characterized by drug resistant seizures, delayed developmental skills, and intellective disability. This group of disorders includes early infantile epileptic encephalopathy also known as Ohtahara syndrome, early myoclonic encephalopathy, epilepsy of infancy with migrating focal seizures, infantile spasms syndrome (also known as West syndrome), severe myoclonic epilepsy in infancy (also known as Dravet syndrome) and, myoclonic encephalopathies in non-progressive disorder. Here we report on seizures manifesting in the first year of life including the neonatal period. Conditions with a benign course, and those with severe evolution are presented. At this early age, clinical identification of seizures, distinction of each of these disorders, type of treatment and prognosis is particularly challenging. The aim of this report is to present the clinical manifestations of each of these disorders and provide an updated review of the conditions associated with seizures in the first year of life.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.