Results 171 to 180 of about 280,776 (352)

Cochlear implant in patients with autistic spectrum disorder-a systematic review. [PDF]

Braz J Otorhinolaryngol, 2021
Tavares FDS, Azevedo YJ, Fernandes LDMM, Takeuti A, Pereira LV, Ledesma ALL, Bahmad F.   +6 more
europepmc   +1 more source

Heterogeneity of subclinical autistic traits among parents of children with autism spectrum disorder: Identifying the broader autism phenotype with a data‐driven method

Autism Research, 2017
E. Bora, Aydan Aydin, Tuğba Saraç, M. Kadak, S. Köse   +4 more
semanticscholar   +1 more source

Behavioral and epileptic phenotypes in a CHD2‐related developmental delay model

Epilepsia, EarlyView.
Abstract Objective Heterozygous loss‐of‐function mutations in the CHD2 gene, encoding chromodomain helicase DNA‐binding protein 2, are associated with severe childhood onset epilepsy, global developmental delay, and autistic features. Animal models that accurately recapitulate human phenotypes are crucial for understanding rare neurodevelopmental ...
Anat Mavashov, Shaked Turk, Yael Sarusi, Marina Brusel, Rotem Ben Tov Perry, Shir Quinn, Yael Almog, Karni Vilian, Mor Yam, Igor Ulitsky, Moran Rubinstein   +10 more
wiley   +1 more source

Music-Enhanced Emotion Identification of Facial Emotions in Autistic Spectrum Disorder Children: A Pilot EEG Study. [PDF]

Brain Sci, 2022
Ramirez-Melendez R, Matamoros E, Hernandez D, Mirabel J, Sanchez E, Escude N.   +5 more
europepmc   +1 more source

Spontaneous recovery in Autistic Spectrum Disorders - A myth?

, 2010
MN Helal, Imran Mushtaq, Srivarshini Sankar   +2 more
openalex   +1 more source

RE: “PRENATAL EXPOSURE TO ACETAMINOPHEN AND RISK FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER AND AUTISTIC SPECTRUM DISORDER: A SYSTEMATIC REVIEW, META-ANALYSIS, AND META-REGRESSION ANALYSIS OF COHORT STUDIES” [PDF]

, 2018
Per Damkier
openalex   +1 more source

From Brain Health to Brain Economy

Brain Health, EarlyView.
Yongjun Wang
wiley   +1 more source

Memantine treatment in individuals with GRIN gain‐of‐function variants is associated with improvements in behavior, development, and seizure frequency

Epilepsia, EarlyView.
Abstract Objective GRIN‐related disorders due to pathogenic variants in GRIN1, GRIN2A, GRIN2B, or GRIN2D genes are associated with altered N‐methyl‐D‐aspartate receptor (NMDAR) function. Functional changes include gain (GoF) and loss of receptor function (LoF). Clinical reports describing the use of the NMDAR blocker memantine in GRIN‐related disorders
Maike Karnstedt, Riley E. Perszyk, Scott J. Myers, Ellington McDaniels, Marta Somorai, Ingo Borggraefe, Danielle C. M. Veenma, An‐Sofie Schoonjans, Pasquale Striano, Tadeu A. Fantaneanu, Steffen Syrbe, Kristen Park, Wenjuan Chen, Hongjie Yuan, Stephen F. Traynelis, Timothy A. Benke, Johannes R. Lemke, Ilona Krey   +17 more
wiley   +1 more source

Amino Acid Patterns in Children with Autistic Spectrum Disorder: A Preliminary Biochemical Evaluation. [PDF]

Nutrients
Ferraro S, Saielli L, Biganzoli D, Tosi M, Guidi L, Longo R, Severino F, Carelli S, Rossi M, Pisciotta L, Ricci E, Brustia F, Verduci E, Zuccotti G, Mussap M, Cereda C.   +15 more
europepmc   +1 more source

Examining the relationship between autistic spectrum disorder characteristics and structural brain differences seen in anorexia nervosa. [PDF]

Eur Eat Disord Rev, 2022
Halls D, Leppanen J, Kerr-Gaffney J, Simic M, Nicholls D, Mandy W, Williams S, Tchanturia K.   +7 more
europepmc   +1 more source