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Damien Wright; Aisling Kenny; Lindsay A. M. Mizen; Andrew G. McKechanie; Andrew C. Stanfield – Journal of Autism and Developmental Disorders, 2025
SYNGAP1-related ID is a genetic condition characterised by global developmental delay and epilepsy. Individuals with SYNGAP1-related ID also commonly show differences in attention and social communication/interaction and frequently receive additional diagnoses of Autism Spectrum Disorder (ASD) or Attention Deficit Hyperactivity Disorder (ADHD). We…
Descriptors: Autism Spectrum Disorders, Attention Deficit Hyperactivity Disorder, Symptoms (Individual Disorders), Children
Michela Tinelli M; Aine Roddy; Martin Knapp; Celso Arango; Maria Andreina Mendez; James Cusack; Declan Murphy; Roberto Canitano; Bethany Oakley; Vinciane Quoidbach – Journal of Autism and Developmental Disorders, 2024
We examine the cost-effectiveness of treating epilepsy with anti-epileptic medicines in autistic children, looking at impacts on healthcare providers (in England, Ireland, Italy and Spain) and children's families (in Ireland). We find carbamazepine to be the most cost-effective drug to try first in children with newly diagnosed focal seizures. For…
Descriptors: Foreign Countries, Autism Spectrum Disorders, Epilepsy, Pharmacology
Freedman, Daniel A.; Terry, Debbie; Enciso, Laurie; Trott, Kristen; Burch, Mary; Albert, Dara V. F. – Journal of Autism and Developmental Disorders, 2023
This is a retrospective case series of pediatric patients referred to the psychogenic nonepileptic events clinic (PNEE) who had comorbid diagnoses of autism spectrum disorder (ASD) or intellectual disability (ID). We describe 15 patients, nine with ASD and six with ID who had a telephone visit follow-up at 12 months. There were higher rates of…
Descriptors: Children, Pediatrics, Patients, Autism Spectrum Disorders
Alabaf, Setareh; Gillberg, Christopher; Lundström, Sebastian; Lichtenstein, Paul; Kerekes, Nóra; Råstam, Maria; Anckarsäter, Henrik – Journal of Autism and Developmental Disorders, 2019
With increasing numbers of children being diagnosed with neurodevelopmental disorders (NDDs) attention has been drawn to these children's physical health. We aimed to identify the prevalence of defined physical problems (epilepsy, migraine, asthma, cancer, diabetes, psoriasis, lactose intolerance, celiac disease, diarrhea, constipation, daytime…
Descriptors: Physical Health, Neurological Impairments, Epilepsy, Diseases
Angell, Amber M.; Deavenport-Saman, Alexis; Yin, Larry; Zou, Baiming; Bai, Chen; Varma, Deepthi; Solomon, Olga – Journal of Autism and Developmental Disorders, 2021
Autistic children have a high prevalence of co-occurring mental health, developmental/behavioral, and medical conditions, but research on sex/gender differences has been mixed. We used Florida healthcare claims data to characterize sex differences (female/male) in co-occurring conditions among autistic children ages 1-21 (N = 83,500). After…
Descriptors: Gender Differences, Comorbidity, Mental Health, Incidence
Gadow, Kenneth D.; Perlman, Greg; Weber, Rebecca J. – Journal of Autism and Developmental Disorders, 2017
Examined the psychiatric and clinical correlates of loss of previously acquired skills (regression) as reported by parents of youth with autism spectrum disorder (ASD). Study sample comprised 6- to 18-year old (N = 213) children and adolescents with ASD. Parents reported regression in 77 (36%) youth. A more homogeneous subgroup with regression…
Descriptors: Autism, Pervasive Developmental Disorders, Epilepsy, Intelligence Quotient
Iannuzzi, Dorothea A.; Cheng, Erika R.; Broder-Fingert, Sarabeth; Bauman, Margaret L. – Journal of Autism and Developmental Disorders, 2015
To identify medical problems most commonly presenting to emergency departments among individuals with autism as compared to non-autistic persons across age groups. Data was obtained from the 2010 National Emergency Department database and was analyzed by age categories: 3-5, 6-11, 12-15, 16-18 and 19 years and older. Epilepsy emerged as the…
Descriptors: Autism, Pervasive Developmental Disorders, Children, Adolescents
Hirota, Tomoya; Veenstra-VanderWeele, Jeremy; Hollander, Eric; Kishi, Taro – Journal of Autism and Developmental Disorders, 2014
Electroencephalogram-recorded epileptiform activity is common in children with autism spectrum disorder (ASD), even without clinical seizures. A systematic literature search identified 7 randomized, placebo-controlled trials of antiepileptic drugs (AEDs) in ASD (total n = 171), including three of valproate, and one each of lamotrigine,…
Descriptors: Autism, Pervasive Developmental Disorders, Drug Therapy, Epilepsy
Atladóttir, H. Ó.; Schendel, D. E.; Parner, E. T.; Henriksen, T. B. – Journal of Autism and Developmental Disorders, 2015
The aim of this study was to describe the profile of specific neonatal morbidities in children later diagnosed with autism spectrum disorder (ASD), and to compare this profile with the profile of children with hyperkinetic disorder, cerebral palsy, epilepsy or intellectual disability. This is a Danish population based cohort study, including all…
Descriptors: Autism, Pervasive Developmental Disorders, Neonates, Child Health
Jokiranta, Elina; Sourander, Andre; Suominen, Auli; Timonen-Soivio, Laura; Brown, Alan S.; Sillanpää, Matti – Journal of Autism and Developmental Disorders, 2014
The present population-based study examines associations between epilepsy and autism spectrum disorders (ASD). The cohort includes register data of 4,705 children born between 1987 and 2005 and diagnosed as cases of childhood autism, Asperger's syndrome or pervasive developmental disorders--not otherwise specified. Each case was matched to four…
Descriptors: Correlation, Epilepsy, Autism, Pervasive Developmental Disorders
Mouridsen, Svend Erik; Rich, Bente; Isager, Torben – Journal of Autism and Developmental Disorders, 2012
We compared the prevalence and types of fractures in a clinical sample of 118 individuals diagnosed as children with infantile autism (IA) with 336 matched controls from the general population. All participants were screened through the nationwide Danish National Hospital Register. The average observation time was 30.3 years (range 27.3-30.4…
Descriptors: Autism, Hospitals, Incidence, Epilepsy
Baghdadli, Amaria; Assouline, Brigitte; Sonie, Sandrine; Pernon, Eric; Darrou, Celine; Michelon, Cecile; Picot, Marie-Christine; Aussilloux, Charles; Pry, Rene – Journal of Autism and Developmental Disorders, 2012
This study examines change in 152 children over an almost 10-year period (T1: 4.9 (plus or minus 1.3) years; T2: 8.1 (plus or minus 1.3) years; T3: 15(plus or minus 1.6) years) using a group-based, semi-parametric method in order to identify distinct developmental trajectories. Important deficits remain at adolescence in the adaptive abilities of…
Descriptors: Early Intervention, Autism, Multivariate Analysis, Language Skills
Giannotti, Flavia; Cortesi, Flavia; Cerquiglini, Antonella; Miraglia, Daniela; Vagnoni, Cristina; Sebastiani, Teresa; Bernabei, Paola – Journal of Autism and Developmental Disorders, 2008
This study investigated sleep of children with autism and developmental regression and the possible relationship with epilepsy and epileptiform abnormalities. Participants were 104 children with autism (70 non-regressed, 34 regressed) and 162 typically developing children (TD). Results suggested that the regressed group had higher incidence of…
Descriptors: Epilepsy, Autism, Sleep, Developmental Disabilities
Peer reviewedGillberg, Christopher – Journal of Autism and Developmental Disorders, 1991
Sixty-six patients under age 25 with autism and epileptic seizures were treated and followed for 2 years. The cases are analyzed in terms of type of epilepsy, drugs used, and other treatments given. Practical guidelines are offered for the management of epilepsy in autism. (Author/JDD)
Descriptors: Adolescents, Autism, Children, Drug Therapy
Peer reviewedKanner, Andres M. – Journal of Autism and Developmental Disorders, 2000
This commentary reviews studies of children with Landau-Kleffner Syndrome (LKS) and autistic regression (AR) and concludes that they are two distinct entities with different epileptic profiles and that the treatment modalities used in LKS cannot be expected to yield a therapeutic effect in AR. Multiple Subpial Transection is discussed. (Contains…
Descriptors: Autism, Children, Epilepsy, Individual Characteristics
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