Results 91 to 100 of about 1,118,223 (234)

Faces do not capture special attention in children with autism spectrum disorder: a change blindness study [PDF]

, 2009
Two experiments investigated attention of children with autism spectrum disorder (ASD) to faces and objects. In both experiments, children (7- to 15-year-olds) detected the difference between 2 visual scenes.
Hasegawa, T., Tojo, Y., Kikuchi, Y., Senju, Atsushi, Osanai, H.   +4 more
core   +1 more source

Disordered eating in autistic trans and gender diverse people: a lived experience-led scoping review

Journal of Eating Disorders
Background This lived experience-led scoping review explores the evidence base related to eating disorders/disordered eating behaviours in Autistic trans and gender diverse (TGD) people.
Luka C. J. White, Kai Schweizer, Kai S. Thomas   +2 more
doaj   +1 more source

Penerapan Latihan Sensorimotor Untuk Meningkatkan Kemampuan Menulis Pada Anak Autistic Spectrum Disorder

Jurnal Pendidikan dan Kebudayaan, 2011
The goal of this research is to prove that the application of sensorimotor training can improve writing skills and the writing in Autistic Spectrum Disorder (ASD) children, the research question posed is: Does the application of sensory motor training ...
Musjafak Assjari, Eva Siti Sopariah
doaj   +1 more source

ADNP‐Related Helsmoortel–Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman, Ana Kolevzon, Paige Siper, Tess Levy, Jeffrey M. Saland, Yitzchak Frank, Robert Rapaport, Kayla Kupietzky, William E. Bennett Jr, Bruce Gelb, Sandra Bedrosian Sermone, Alexander Kolevzon   +11 more
wiley   +1 more source

Altered gut microbiota and short chain fatty acids in Chinese children with autism spectrum disorder

Scientific Reports, 2019
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is characterized by impairments in social interactions and communication, restricted interests and repetitive behaviors. Several studies report a high prevalence of gastrointestinal (GI)
Simeng Liu, Enyao Li, Zhenyu Sun, Dongjun Fu, Guiqin Duan, Miaomiao Jiang, Yong Yu, Lu Mei, Pingchang Yang, Youcai Tang, Pengyuan Zheng   +10 more
doaj   +1 more source

Instruments for augmentative and alternative communication for children with autism spectrum disorder: a systematic review

Clinics, 2018
New technologies designed to improve the communication of autistic children can also help to promote interaction processes and cognitive and social development. The aim of this study was to analyze the instruments used to improve the communication skills
Jennifer Yohanna Ferreira de Lima Antão, Acary Souza Bulle Oliveira, Renata Thaís de Almeida Barbosa, Tânia Brusque Crocetta, Regiani Guarnieri, Claudia Arab, Thaís Massetti, Thaiany Pedrozo Campos Antunes, Alan Patrício da Silva, ĺtalla Maria Pinheiro Bezerra, Carlos Bandeira de Mello Monteiro, Luiz Carlos de Abreu   +11 more
doaj   +1 more source

Severe Headbanging Responsive to Levodopa in a Child With FOXP1 Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We report a 9‐year‐old female with FOXP1 syndrome due to a de novo in‐frame deletion in the FOXP1 gene. The child has a severe neurodevelopmental disorder including global developmental delay and autism spectrum disorder. At age 2, she developed severe headbanging, which was progressive and did not respond to multidisciplinary, behavioral ...
Pamela Veale, Christopher Tiessen, Vithya Gnanakumar   +2 more
wiley   +1 more source

First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa, Joana Rosa Marques Prota, Antonia Paula Marques‐de‐Faria, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source

Selective attention and perceptual load in autism spectrum disorder [PDF]

, 2010
This thesis examines selective attention in young adults with Autism Spectrum Disorder (ASD). Existing literature regarding this issue is mixed; some research suggesting an overly-focused attentional style (Rincover & Ducharme, 1987) while others ...
Remington, A.M.
core  

Strong genetic influences on the stability of autistic traits in childhood [PDF]

, 2014
Objective: Disorders on the autism spectrum, as well as autistic traits in the general population, have been found to be both highly stable across age and highly heritable at individual ages.
Ronald, Angelica, Plomin, Robert, Plomin, R., Ronald, A, Plomin, R, Hallett, V, Rijsdijk, FV, Holmboe, Karla, Happé, Francesca, Happ�, F, Holmboe, K, Ronald, A., Hallett, Victoria, Rijsdijk, F., Hallett, V., Rijsdijk, Fruhling V., Happé, F., Holmboe, K., Rijsdijk, F.V.   +18 more
core   +1 more source