Results 151 to 160 of about 24,501 (230)

Remote microphone systems in children and adolescents with autism spectrum disorders: a scoping review. [PDF]

Codas
Vital BSB, Santos KMGD, Araújo ADDSN, Brazorotto JS, Jacob RTS, Taveira KVM, Balen SA.   +6 more
europepmc   +1 more source

Autism spectrum disorder-associated Sema5A p.Arg676Cys drives Arf6/FE65 signaling and aberrant cell morphogenesis. [PDF]

Sci Rep
Takahashi M, Yako H, Miyamoto Y, Kukimoto-Niino M, Shirouzu M, Yamauchi J.   +5 more
europepmc   +1 more source

Reading Autism [PDF]

, 2007
Mcgrath, JP
core  

Severe Renal Phenotype Across A Multigenerational Tuberous Sclerosis Complex (TSC) Family. [PDF]

Mol Genet Genomic Med
Tuller E, Samuels JA, Northrup H, Richardson K.   +3 more
europepmc   +1 more source

Unveiling autism spectrum disorder for the pediatrician. [PDF]

J Pediatr (Rio J)
Vasconcelos MM, Vasconcelos LGA, Brito AR.   +2 more
europepmc   +1 more source

Fetal Growth Restriction, Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder-Connecting the Dots: A Narrative Review. [PDF]

Children (Basel)
Kozonis A, Papadoliopoulou M, Margaris I.   +2 more
europepmc   +1 more source

Mechanistic strategies for secondary prevention of developmental and epileptic encephalopathy in children with tuberous sclerosis complex. [PDF]

EBioMedicine
Specchio N, Di Micco V, Scheper M, Aronica E, Curatolo P.   +4 more
europepmc   +1 more source

Predicting parental caregiving burden based on sensory processing patterns and social skills in individuals with high-functioning autism spectrum disorder. [PDF]

Front Psychiatry
Zhang S, Zhang L, Li Y, Zhang Y, Su L.
europepmc   +1 more source

Genetic, Clinical and Neuroradiological Spectrum of MED-Related Disorders: An Updated Review. [PDF]

Genes (Basel)
Fazio A, Leonardi R, Aliotta L, Lo Bianco M, Anastasio G, Messina G, Spatola C, Foti PV, Palmucci S, Basile A, Ruggieri M, David E.   +11 more
europepmc   +1 more source

Incomplete penetrance and variable phenotypes of a novel NPRL2 frameshift variant: from familial focal epilepsy with variable foci 2 to neurodevelopmental disorders. [PDF]

BMC Neurol
Zhu H, Wang Q, Deng W, Zhu S, Zeng L, Chen A, Pang Y, Xiong F.   +7 more
europepmc   +1 more source