Pages that link to "Q48408503"
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The following pages link to Autism: a mitochondrial disorder? (Q48408503):
Displaying 50 items.
- The Screening and Diagnosis of Autistic Spectrum Disorders (Q22251344) (← links)
- Childhood autism and associated comorbidities (Q22252337) (← links)
- Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis (Q24630557) (← links)
- Autistic spectrum disorders and mitochondrial encephalopathies (Q28282764) (← links)
- Mitochondrial disease in autism spectrum disorder patients: a cohort analysis (Q28474112) (← links)
- The NADH‐ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism (Q34136776) (← links)
- The contribution of mitochondria to common disorders (Q34271106) (← links)
- A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism (Q34273431) (← links)
- Downregulation of the expression of mitochondrial electron transport complex genes in autism brains. (Q34307534) (← links)
- Embryo toxicity and teratogenicity of formaldehyde (Q34381463) (← links)
- Lipidomic analysis and electron transport chain activities in C57BL/6J mouse brain mitochondria (Q35013455) (← links)
- Genetics and Mitochondrial Abnormalities in Autism Spectrum Disorders:A Review (Q35132741) (← links)
- Mitochondrial Dysfunction Can Connect the Diverse Medical Symptoms Associated With Autism Spectrum Disorders (Q35232104) (← links)
- Energetics, epigenetics, mitochondrial genetics (Q35632855) (← links)
- Should autistic children be evaluated for mitochondrial disorders? (Q35821629) (← links)
- Dysautonomia in Autism Spectrum Disorder: Case Reports of a Family with Review of the Literature (Q36168998) (← links)
- Mitochondrial and ion channel gene alterations in autism. (Q36178457) (← links)
- Brain region-specific altered expression and association of mitochondria-related genes in autism (Q36483260) (← links)
- Evaluating mitochondrial DNA variation in autism spectrum disorders (Q36503894) (← links)
- A prospective double-blind, randomized clinical trial of levocarnitine to treat autism spectrum disorders (Q36516455) (← links)
- Nanotechnology inspired tools for mitochondrial dysfunction related diseases (Q36703351) (← links)
- Brain region-specific deficit in mitochondrial electron transport chain complexes in children with autism (Q36820898) (← links)
- Role of NAD( ), Oxidative Stress, and Tryptophan Metabolism in Autism Spectrum Disorders (Q37059666) (← links)
- Gestational exposure to a viral mimetic poly(i:C) results in long-lasting changes in mitochondrial function by leucocytes in the adult offspring (Q37221940) (← links)
- Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism (Q37280803) (← links)
- Neurometabolic disorders and dysfunction in autism spectrum disorders (Q37408409) (← links)
- Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction (Q37433527) (← links)
- Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure. (Q37607012) (← links)
- Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome (Q37680843) (← links)
- Epigenetic Treatment of Neuropsychiatric Disorders: Autism and Schizophrenia. (Q38743021) (← links)
- Mitochondrial Dysfunction in Autism Spectrum Disorders (Q39032450) (← links)
- Evidence of Mitochondrial Dysfunction in Autism: Biochemical Links, Genetic-Based Associations, and Non-Energy-Related Mechanisms. (Q39384617) (← links)
- Dietary DHA, bioaccessibility, and neurobehavioral development in children (Q39407110) (← links)
- Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis (Q39432351) (← links)
- An aetiological study of 25 mentally retarded adults with autism. (Q42705242) (← links)
- Pathophysiological role of nitric oxide and adrenomedullin in autism (Q44310380) (← links)
- Changes in nitric oxide levels and antioxidant enzyme activities may have a role in the pathophysiological mechanisms involved in autism (Q44401087) (← links)
- Altered heavy metals and transketolase found in autistic spectrum disorder (Q49051227) (← links)
- Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion (Q49843158) (← links)
- MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation (Q50301776) (← links)
- Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene (Q50302132) (← links)
- Proton magnetic resonance spectroscopy and MRI reveal no evidence for brain mitochondrial dysfunction in children with autism spectrum disorder (Q50312134) (← links)
- Neurologic presentations of mitochondrial disorders (Q52171605) (← links)
- Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: A possible role of fluoride and aluminum. (Q55079878) (← links)
- The Emerging Field of Nutritional Mental Health (Q56675883) (← links)
- Impaired neurite development associated with mitochondrial dysfunction in dopaminergic neurons differentiated from exfoliated deciduous tooth-derived pulp stem cells of children with autism spectrum disorder (Q58706246) (← links)
- Autism and carnitine: A possible link (Q60920089) (← links)
- Redox Mechanisms in Neurodegeneration: From Disease Outcomes to Therapeutic Opportunities (Q88316783) (← links)
- New Horizons for Molecular Genetics Diagnostic and Research in Autism Spectrum Disorder (Q89477342) (← links)
- Protein Nutrition in Autism (Q89477418) (← links)