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Recent advances in the pathogenesis of syndromic autismsMitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysisA Short Review on the Current Understanding of Autism Spectrum DisordersThe molecular basis of cognitive deficits in pervasive developmental disordersCan psychiatric childhood disorders be due to inborn errors of metabolism?Evidence for treatable inborn errors of metabolism in a cohort of 187 Greek patients with autism spectrum disorder (ASD).Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?Cognitive development in patients with Mucopolysaccharidosis type III (Sanfilippo syndrome).Genetics and mitochondrial abnormalities in autism spectrum disorders: a review.The pathogenesis of autism.Mitochondrial dysfunction can connect the diverse medical symptoms associated with autism spectrum disorders.One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disordersGWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican AmericansAssessment and treatment in autism spectrum disorders: a focus on genetics and psychiatryGenetics and the myth of vaccine encephalopathyOlfactory stem cells reveal MOCOS as a new player in autism spectrum disorders.Neuropsychological Development in Patients with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency.Communication Impairments in Children with Inborn Errors of Metabolism: A Preliminary Study.Autism spectrum disorders--a genetics review.A review of candidate urinary biomarkers for autism spectrum disorder.Autism spectrum disorders: the quest for genetic syndromes.Neurodegenerative disorders and metabolic disease.A blueprint for research on Shankopathies: a view from research on autism spectrum disorder.Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder.A scoping review of what is known of the physical health of adults with autism spectrum disorder.ADHD, autism and neuroradiological complications among phenylketonuric children in Upper Egypt.Inherited metabolic disorders in Turkish patients with autism spectrum disorders.Identification of an age-dependent biomarker signature in children and adolescents with autism spectrum disorders.Autism spectrum disorder secondary to enterovirus encephalitis.Uptake and Diagnostic Yield of Chromosomal Microarray in an Australian Child Development Clinic.Integrated approach to yoga therapy and autism spectrum disordersAutism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects.Audit of Organic Acidurias from a Single Centre: Clinical and Metabolic Profile at Presentation with Long Term Outcome.Inborn error metabolic screening in individuals with nonsyndromic autism spectrum disorders.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Autism and Metabolic Diseases
@ast
Autism and Metabolic Diseases
@en
Autism and Metabolic Diseases
@nl
type
label
Autism and Metabolic Diseases
@ast
Autism and Metabolic Diseases
@en
Autism and Metabolic Diseases
@nl
altLabel
Autism and metabolic diseases
@en
prefLabel
Autism and Metabolic Diseases
@ast
Autism and Metabolic Diseases
@en
Autism and Metabolic Diseases
@nl
P2093
P2860
P3181
P356
P1476
Autism and Metabolic Diseases
@en
P2093
A. L. Loizzo
P. Curatolo
P2860
P304
P3181
P356
10.1177/0883073807308698
P407
P577
2008-01-11T00:00:00Z