Autism spectrum disorder and epilepsy: Disorders with a shared biology.
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Identification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes.Potassium Channels and Human Epileptic Phenotypes: An Updated OverviewWhole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathiesDrosophila Homolog of Human KIF22 at the Autism-Linked 16p11.2 Loci Influences Synaptic Connectivity at Larval Neuromuscular Junctions.Autism and epilepsy: A population-based nationwide cohort study.RNA activation of haploinsufficient Foxg1 gene in murine neocortex.Altered Intermittent Rhythmic Delta and Theta Activity in the Electroencephalographies of High Functioning Adult Patients with Autism Spectrum Disorder.Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.Neurobehavioral comorbidities of epilepsy: Role of inflammation.Cognitive and neurodevelopmental comorbidities in paediatric epilepsy.Dysfunction of sensory oscillations in Autism Spectrum DisorderInflammatory aspects of epileptogenesis: contribution of molecular inflammatory mechanisms.Autism, epilepsy, and synaptopathies: a not rare association.Epilepsy in patients with autism: links, risks and treatment challenges.Multidimensional Neuroanatomical Subtyping of Autism Spectrum Disorder.Phenotype Differentiation of FOXG1 and MECP2 Disorders: A New Method for Characterization of Developmental Encephalopathies.Relation of Psychiatric Symptoms with Epilepsy, Asthma, and Allergy in Youth with ASD vs. Psychiatry Referrals.Prevalence and risk factors for autism spectrum disorder in epilepsy: a systematic review and meta-analysis.The transcription factor NeuroD2 coordinates synaptic innervation and cell intrinsic properties to control excitability of cortical pyramidal neurons.Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.Enhancing Neuronogenesis and Counteracting Neuropathogenic Gene Haploinsufficiencies by RNA Gene Activation.PLXNA1 developmental encephalopathy with syndromic features: A case report and review of the literature.CNTNAP2 stabilizes interneuron dendritic arbors through CASK.Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.
P2860
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P2860
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@ast
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@en
type
label
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@ast
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@en
prefLabel
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@ast
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@en
P2093
P2860
P1433
P1476
Autism spectrum disorder and epilepsy: Disorders with a shared biology.
@en
P2093
Alex R Paciorkowski
Bo Hoon Lee
Tristram Smith
P2860
P304
P356
10.1016/J.YEBEH.2015.03.017
P577
2015-04-19T00:00:00Z