Developmental regression and mitochondrial dysfunction in a child with autism - Wikidata - awgldk - TriplyDB

Developmental regression and mitochondrial dysfunction in a child with autism

Developmental regression and mitochondrial dysfunction in a child with autism

http://www.wikidata.org/entity/Q34505872

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A broken trust: lessons from the vaccine--autism wars Biomarkers in autism B-lymphocytes from a population of children with autism spectrum disorder and their unaffected siblings exhibit hypersensitivity to thimerosal Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis Identification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes.Autistic spectrum disorders and mitochondrial encephalopathies Oxidative pathways as a drug target for the treatment of autism A comparison of temporal trends in United States autism prevalence to trends in suspected environmental factors Mitochondrial disease in autism spectrum disorder patients: a cohort analysis Toward a theory of childhood learning disorders, hyperactivity, and aggression Can psychiatric childhood disorders be due to inborn errors of metabolism?Cochlear Implantation in Children With Autism Spectrum Disorder Enteric short-chain fatty acids: microbial messengers of metabolism, mitochondria, and mind: implications in autism spectrum disorders.Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Plasma membrane coenzyme Q: evidence for a role in autism.Treatments for biomedical abnormalities associated with autism spectrum disorder.15q11.2-13 duplication, mitochondrial dysfunction, and developmental disorders Downregulation of the expression of mitochondrial electron transport complex genes in autism brains.Measuring the maturity of the fast-spiking interneuron transcriptional program in autism, schizophrenia, and bipolar disorder Mitochondrial dysfunction can connect the diverse medical symptoms associated with autism spectrum disorders.Energetics, epigenetics, mitochondrial genetics.Mitochondrial and ion channel gene alterations in autism.Evaluating mitochondrial DNA variation in autism spectrum disorders.Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010 Potency of pre-post treatment of coenzyme Q10 and melatonin supplement in ameliorating the impaired fatty acid profile in rodent model of autism Brain region-specific deficit in mitochondrial electron transport chain complexes in children with autism.Genetics and the myth of vaccine encephalopathy The neonatal levels of TSB, NSE and CK-BB in autism spectrum disorder from Southern China Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism.Annual report on adverse events related with vaccines use in Calabria (Italy): 2012.Assessing bioenergetic compromise in autism spectrum disorder with 31P magnetic resonance spectroscopy: preliminary report.Metabolic Dysfunction Underlying Autism Spectrum Disorder and Potential Treatment Approaches.Neurodevelopmental manifestations of mitochondrial disease.Human papilloma virus vaccine and primary ovarian failure: another facet of the autoimmune/inflammatory syndrome induced by adjuvants.The Ethics Writings of Roger A. Brumback, MD.Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population.Novel biomarkers of metabolic dysfunction is autism spectrum disorder: potential for biological diagnostic markers.Predictive value of selected biomarkers related to metabolism and oxidative stress in children with autism spectrum disorder.Comparative efficacy of alpha-linolenic acid and gamma-linolenic acid to attenuate valproic acid-induced autism-like features.

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P2860

Developmental regression and mitochondrial dysfunction in a child with autism

http://www.wikidata.org/entity/Q34505872

description

2006 nî lūn-bûn

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2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2006 թվականի փետրվարին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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type

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Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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Developmental regression and mitochondrial dysfunction in a child with autism

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Journal of Child Neurology

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Developmental regression and mitochondrial dysfunction in a child with autism

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P2093

Andrew W Zimmerman

http://www.w3.org/2001/XMLSchema#string

John Shoffner

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Jon S Poling

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Richard E Frye

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P2860

Developmental regression in autism spectrum disorders.

Should autistic children be evaluated for mitochondrial disorders?

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies.

Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome.

Mitochondrial dysfunction in autistic patients with 15q inverted duplication.

Neuropathology of Rett syndrome: case report with neuronal and mitochondrial abnormalities in the brain.

Infantile hypotonia as a presentation of Rett syndrome.

Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation.

Mitochondrial DNA abnormalities and autistic spectrum disorders.

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