Results 31 to 40 of about 59,438 (255)

Investigating autism etiology and heterogeneity by decision tree algorithm

Informatics in Medicine Unlocked, 2019
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that causes deficits in cognition, communication and social skills. ASD, however, is a highly heterogeneous disorder.
Mariam M. Hassan, Hoda M.O. Mokhtar
doaj   +1 more source

Disentangling Restrictive and Repetitive Behaviors and Social Impairments in Children and Adolescents with Gilles de la Tourette Syndrome and Autism Spectrum Disorder

Brain Sciences, 2020
Gilles de la Tourette syndrome (GTS) and autism spectrum disorder (ASD) are two neurodevelopmental disorders with male predominance, frequently comorbid, that share clinical and behavioral features.
Mariangela Gulisano, Rita Barone, Salvatore Alaimo, Alfredo Ferro, Alfredo Pulvirenti, Lara Cirnigliaro, Selena Di Silvestre, Serena Martellino, Nicoletta Maugeri, Maria Chiara Milana, Miriam Scerbo, Renata Rizzo   +11 more
doaj   +1 more source

Intravenous secretin for autism spectrum disorders (ASD) [PDF]

Cochrane Database of Systematic Reviews, 2012
In 1998 secretin, a gastrointestinal hormone, was suggested as an effective treatment for autism spectrum disorders (ASD) based on anecdotal evidence.To assess whether intravenous secretin improves the core features of ASD, other aspects of behaviour or function such as self-injurious behaviour, and the quality of life of affected individuals and their
Katrina, Williams, John A, Wray, Danielle M, Wheeler   +2 more
openaire   +2 more sources

Personality disorder in autism spectrum disorder : myth or reality?

European Psychiatry, 2023
Introduction Autism spectrum disorder is a neurodevelopmental disorder characterized by persistent deficit in communication and social interaction associated with repetitive, restricted interests, behaviors or activities.
N. Kouki, A. Maamri, S. Cherif, E. Cherif, H. Zalila   +4 more
doaj   +1 more source

The autism spectrum disorders (ASD) [PDF]

Italian Journal of Pediatrics, 2014
Screening within the 2nd year of life ( primarily between 12 and 18 months ) is a tool for early detection of the risk of a neurobehavioral developmental disorder and is a chance to change the term prognosis of ASD. The Analysis of the interactions of functional and dysfunctional interactive communicative signals from the very early ages of life, as
openaire   +1 more source

Modulation of Homer1 EVH1 domain internal dynamics by putative autism‐associated mutations

FEBS Letters, EarlyView.
The putative autism‐associated M65I and S97L variants of the EVH1 domain of the postsynaptic scaffold protein Homer1 do not exhibit substantial changes in their overall structure or partner binding. Both of them, but especially the M65I variant, show altered internal dynamics relative to the wild‐type domain on the μs‐ms timescale, indicated by the ...
Fanni Farkas, Brigitta Maruzs, Zsófia E. Kálmán, Tomas Klumpler, Gyula Batta, Bálint Péterfia, Zoltán Gáspári   +6 more
wiley   +1 more source

A Convolutional Deep Neural Network Approach to Predict Autism Spectrum Disorder Based on Eye-Tracking Scan Paths

Information
Autism spectrum disorder (ASD) is a developmental disorder that encompasses difficulties in communication (both verbal and non-verbal), social skills, and repetitive behaviors.
May Alsaidi, Nadim Obeid, Nailah Al-Madi, Hazem Hiary, Ibrahim Aljarah   +4 more
doaj   +1 more source

Evaluation of Children with Autism Spectrum Disorder by using Common Brief Core Sets of International Classification of Functioning, Disability, and Health for Children and Youth (ICF-CY)

Pakistan Armed Forces Medical Journal, 2023
Objective: To evaluate children with Autism Spectrum Disorder (ASD) by using Common Brief Core Sets of International Classification of Functioning, Disability, and Health for Children and Youth (ICF-CY) Study Design: Cross-sectional study Place ...
Sidra Tahir, Shazia Maqbool, Aisha Farid, Anam Ali, Ehsan Ullah, Hina Azhar   +5 more
doaj   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina, Anna Marcé‐Grau, Barbara Masotto, Marta Codina, Lamia BenJemaa, Yasmina Elaribi, Mónica Martinez‐Gallo, Roger Colobran, Angel Sanchez‐Montañez, Irene Valenzuela, Yoshiko Murakami, Alfons Macaya   +11 more
wiley   +1 more source

Electroencephalographic Normalization as a Biomarker of Clinical Recovery in Down Syndrome Regression Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Down syndrome regression disorder is a syndrome characterized by subacute loss of cognitive, behavioral, and functional abilities in individuals with Down syndrome. Electroencephalography abnormalities are frequently observed during evaluation, but it remains unclear whether these findings represent a dynamic marker of disease ...
Jonathan D. Santoro, Mackenzie Silverman, Maeve C. Lucas, Mariam M. Yousuf, Samuel T. Otey, Stella V. Gray, Brittany Jordan, Madeline D. Kahan, Latanya D. Agurs, Michelle Van Hirtum Das, Deborah Holder, Devin King, Eileen A. Quinn, Ryan Kammeyer, Michael S. Rafii   +14 more
wiley   +1 more source