Related references
Note: Only part of the references are listed.Folinic acid improves verbal communication in children with autism and language impairment: a randomized double-blind placebo-controlled trial
R. E. Frye et al.
MOLECULAR PSYCHIATRY (2018)
Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion
Noemi Agnes Varga et al.
BEHAVIORAL AND BRAIN FUNCTIONS (2018)
Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder
Halil Ibrahim Aydin
INDIAN PEDIATRICS (2018)
Coenzyme Q10 supplementation reduces oxidative stress and decreases antioxidant enzyme activity in children with autism spectrum disorders
Elham Mousavinejad et al.
PSYCHIATRY RESEARCH (2018)
Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder
Matthew A. Budd et al.
VIRUSES-BASEL (2018)
Butyrate enhances mitochondrial function during oxidative stress in cell lines from boys with autism
Shannon Rose et al.
TRANSLATIONAL PSYCHIATRY (2018)
Biomarkers for Detecting Mitochondrial Disorders
Josef Finsterer et al.
JOURNAL OF CLINICAL MEDICINE (2018)
Mitochondrial translation requires folate-dependent tRNA methylation
Raphael J. Morscher et al.
NATURE (2018)
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis
Yanqing Zhang et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2018)
Difference in mitochondrial DNA copy number in peripheral blood cells between probands with autism spectrum disorders and their unaffected siblings
Hee Jeong Yoo et al.
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY (2017)
Mitochondrial and redox abnormalities in autism lymphoblastoid cells: a sibling control study
Shannon Rose et al.
FASEB JOURNAL (2017)
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society
Sumit Parikh et al.
GENETICS IN MEDICINE (2017)
Bioenergetic variation is related to autism symptomatology
Leanna Delhey et al.
METABOLIC BRAIN DISEASE (2017)
Predictive value of selected biomarkers related to metabolism and oxidative stress in children with autism spectrum disorder
Afaf El-Ansary et al.
METABOLIC BRAIN DISEASE (2017)
Novel biomarkers of metabolic dysfunction is autism spectrum disorder: potential for biological diagnostic markers
Asma M. Khemakhem et al.
METABOLIC BRAIN DISEASE (2017)
Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders
Mad Rossi et al.
PEDIATRIC NEUROLOGY (2017)
Assessment of plasma amino acid profile in autism using cation-exchange chromatography with postcolumn derivatization by ninhydrin
Mona Mohamed Zaki et al.
TURKISH JOURNAL OF MEDICAL SCIENCES (2017)
Classification and adaptive behavior prediction of children with autism spectrum disorder based upon multivariate data analysis of markers of oxidative stress and DNA methylation
Daniel P. Howsmon et al.
PLOS COMPUTATIONAL BIOLOGY (2017)
Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders
Dimitra Chalkia et al.
JAMA PSYCHIATRY (2017)
Modulation of Immunological Pathways in Autistic and Neurotypical Lymphoblastoid Cell Lines by the Enteric Microbiome Metabolite Propionic Acid
Richard E. Frye et al.
FRONTIERS IN IMMUNOLOGY (2017)
Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction
Barrett J. Burger et al.
FRONTIERS IN PEDIATRICS (2017)
The Effect of Mitochondrial Supplements on Mitochondrial Activity in Children with Autism Spectrum Disorder
Leanna M. Delhey et al.
JOURNAL OF CLINICAL MEDICINE (2017)
Mitochondrial dysfunction in the gastrointestinal mucosa of children with autism: A blinded case-control study
Shannon Rose et al.
PLOS ONE (2017)
Oxidative Stress Challenge Uncovers Trichloroacetaldehyde Hydrate-Induced Mitoplasticity in Autistic and Control Lymphoblastoid Cell Lines
Richard Eugene Frye et al.
SCIENTIFIC REPORTS (2017)
Role of SIRT1/PGC-1α in mitochondrial oxidative stress in autistic spectrum disorder
Xiaosong Bu et al.
NEUROPSYCHIATRIC DISEASE AND TREATMENT (2017)
Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder
Ashok Patowary et al.
AUTISM RESEARCH (2017)
Mitochondrial Aspartate/Glutamate Carrier SLC25A12 and Autism Spectrum Disorder: a Meta-Analysis
Yuta Aoki et al.
MOLECULAR NEUROBIOLOGY (2016)
Respiratory and autonomic dysfunction in children with autism spectrum disorders
Xue Ming et al.
BRAIN & DEVELOPMENT (2016)
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder
Dora C. Tarlungeanu et al.
CELL (2016)
Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications
V. Oikonomakis et al.
CLINICAL GENETICS (2016)
Cytokines profile and peripheral blood mononuclear cells morphology in Rett and autistic patients
Alessandra Pecorelli et al.
CYTOKINE (2016)
Metabolomics of autism spectrum disorders: early insights regarding mammalian-microbial cometabolites
Michele Mussap et al.
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS (2016)
Autism in patients with propionic acidemia
Peter Witters et al.
MOLECULAR GENETICS AND METABOLISM (2016)
CSF concentrations of 5-methyltetrahydrofolate in a cohort of young children with autism
John Shoffner et al.
NEUROLOGY (2016)
Mitochondrial Copy Number as a Biomarker for Autism?
Christelle Golzio et al.
PEDIATRICS (2016)
Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study
Sarah Wong et al.
PEDIATRICS (2016)
Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder
Yiqin Wang et al.
PLOS GENETICS (2016)
The potential role of nitrous oxide in the etiology of autism spectrum disorder
R. E. Frye et al.
TRANSLATIONAL PSYCHIATRY (2016)
Modulation of mitochondrial function by the microbiome metabolite propionic acid in autism and control cell lines
R. E. Frye et al.
TRANSLATIONAL PSYCHIATRY (2016)
Mitochondrial Dysfunction may explain symptom variation in Phelan-McDermid Syndrome
Richard E. Frye et al.
SCIENTIFIC REPORTS (2016)
Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment
Dmitriy M. Niyazov et al.
MOLECULAR SYNDROMOLOGY (2016)
Identification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes
Richard E. Frye et al.
CLINICAL MEDICINE INSIGHTS-PEDIATRICS (2016)
THE NEONATAL LEVELS OF TSB, NSE AND CK-BB IN AUTISM SPECT RUM DISORDER FROM SOUTHERN CHINA
Meng-na Lv et al.
TRANSLATIONAL NEUROSCIENCE (2016)
Calpain-5 Expression in the Retina Localizes to Photoreceptor Synapses
Kellie A. Schaefer et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2016)
Improvement of Regressive Autism Symptoms in a Child with TMLHE Deficiency Following Carnitine Supplementation
Mark N. Ziats et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)
Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis
Jun Liu et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2015)
Meta-Analysis of Gene Expression in Autism Spectrum Disorder
Carolyn Ch'ng et al.
AUTISM RESEARCH (2015)
Mitochondrial enzyme dysfunction in autism spectrum disorders; a novel biomarker revealed from buccal swab analysis
Michael J. Goldenthal et al.
BIOMARKERS IN MEDICINE (2015)
The many roads to mitochondrial dysfunction in neuroimmune and neuropsychiatric disorders
Gerwyn Morris et al.
BMC MEDICINE (2015)
Elevated mitochondrial DNA copy number in peripheral blood cells is associated with childhood autism
Shan Chen et al.
BMC PSYCHIATRY (2015)
Immune mediated conditions in autism spectrum disorders
Ousseny Zerbo et al.
BRAIN BEHAVIOR AND IMMUNITY (2015)
Mitochondria in the Regulation of Innate and Adaptive Immunity
Samuel E. Weinberg et al.
IMMUNITY (2015)
Autism and Intellectual Disability Associated with Mitochondrial Disease and Hyperlactacidemia
Jose Guevara-Campos et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2015)
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
Kristiina Tammimies et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2015)
Shared Pathways Among Autism Candidate Genes Determined by Co-expression Network Analysis of the Developing Human Brain Transcriptome
Ahmed Mahfouz et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2015)
Homozygosity analysis in subjects with autistic spectrum disorder
Ahmad Adi et al.
MOLECULAR MEDICINE REPORTS (2015)
A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation
Chao Chen et al.
PROTEIN & CELL (2015)
Brain Lactate as a Potential Biomarker for Comorbid Anxiety Disorder in Autism Spectrum Disorder Reply
Bradley S. Peterson et al.
JAMA PSYCHIATRY (2015)
Brain Lactate as a Potential Biomarker for Comorbid Anxiety Disorder in Autism Spectrum Disorder
Stephen R. Dager et al.
JAMA PSYCHIATRY (2015)
Oxidative stress induces mitochondrial dysfunction in a subset of autistic lymphoblastoid cell lines (vol 4, e377, 2014)
S. Rose et al.
TRANSLATIONAL PSYCHIATRY (2015)
AMPD1 functional variants associated with autism in Han Chinese population
Lusi Zhang et al.
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE (2015)
Increased Susceptibility to Ethylmercury-Induced Mitochondrial Dysfunction in a Subset of Autism Lymphoblastoid Cell Lines
Shannon Rose et al.
JOURNAL OF TOXICOLOGY (2015)
Microbiome Disturbances and Autism Spectrum Disorders
Cheryl S. Rosenfeld
DRUG METABOLISM AND DISPOSITION (2015)
Prevalence of antimitochondrial antibodies in autism spectrum subjects
Muhammad Iqbal et al.
FUTURE NEUROLOGY (2015)
Bisphenol A induces oxidative stress and mitochondrial dysfunction in lymphoblasts from children with autism and unaffected siblings
Kulbir Kaur et al.
FREE RADICAL BIOLOGY AND MEDICINE (2014)
The Familial Risk of Autism
Sven Sandin et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2014)
Assessing Bioenergetic Compromise in Autism Spectrum Disorder With 31P Magnetic Resonance Spectroscopy: Preliminary Report
Beatrice A. Golomb et al.
JOURNAL OF CHILD NEUROLOGY (2014)
Inborn errors of metabolism underlying primary immunodeficiencies
Nima Parvaneh et al.
JOURNAL OF CLINICAL IMMUNOLOGY (2014)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis et al.
NATURE (2014)
Ubiquinol Improves Symptoms in Children with Autism (Publication with Expression of Concern. See vol. 2020, 2020)
Anna Gvozdjakova et al.
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY (2014)
Deficits in Bioenergetics and Impaired Immune Response in Granulocytes From Children With Autism
Eleonora Napoli et al.
PEDIATRICS (2014)
Oxidative Stress Induces Mitochondrial Dysfunction in a Subset of Autism Lymphoblastoid Cell Lines in a Well-Matched Case Control Cohort
Shannon Rose et al.
PLOS ONE (2014)
Enteric Bacterial Metabolites Propionic and Butyric Acid Modulate Gene Expression, Including CREB-Dependent Catecholaminergic Neurotransmission, in PC12 Cells - Possible Relevance to Autism Spectrum Disorders
Bistra B. Nankova et al.
PLOS ONE (2014)
Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders
Stefania Gimelli et al.
MOLECULAR CYTOGENETICS (2014)
Mitochondrial Dysfunction as a Neurobiological Subtype of Autism Spectrum Disorder Evidence From Brain Imaging
Suzanne Goh et al.
JAMA PSYCHIATRY (2014)
Protein signatures of oxidative stress response in a patient specific cell line model for autism
Andreas G. Chiocchetti et al.
MOLECULAR AUTISM (2014)
Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome
Jaroslava Durdiakova et al.
MOLECULAR AUTISM (2014)
Oxidative stress induces mitochondrial dysfunction in a subset of autistic lymphoblastoid cell lines
S. Rose et al.
TRANSLATIONAL PSYCHIATRY (2014)
Environmental toxicants and autism spectrum disorders: a systematic review
D. A. Rossignol et al.
TRANSLATIONAL PSYCHIATRY (2014)
Evidence linking oxidative stress, mitochondrial dysfunction, and inflammation in the brain of individuals with autism
Daniel A. Rossignol et al.
FRONTIERS IN PHYSIOLOGY (2014)
Treatments for biomedical abnormalities associated with autism spectrum disorder
Richard Eugene Frye et al.
FRONTIERS IN PEDIATRICS (2014)
The contribution of epigenetics to understanding genetic factors in autism
Layla Hall et al.
AUTISM (2014)
Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders
Athena Hadjixenofontos et al.
ANNALS OF HUMAN GENETICS (2013)
Downregulation of the Expression of Mitochondrial Electron Transport Complex Genes in Autism Brains
Ayyappan Anitha et al.
BRAIN PATHOLOGY (2013)
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions (vol 15, pg 399, 2013)
G. Bradley Schaefer et al.
GENETICS IN MEDICINE (2013)
Cerebral folate receptor autoantibodies in autism spectrum disorder
R. E. Frye et al.
MOLECULAR PSYCHIATRY (2013)
Mitochondrial abnormalities in temporal lobe of autistic brain
Guomei Tang et al.
NEUROBIOLOGY OF DISEASE (2013)
Peripheral blood gene expression signature differentiates children with autism from unaffected siblings
S. W. Kong et al.
NEUROGENETICS (2013)
Autism spectrum disorders associated to a deficiency of the enzymes of the mitochondrial respiratory chain
Jose Guevara-Campos et al.
METABOLIC BRAIN DISEASE (2013)
Altered Metabolites in the Plasma of Autism Spectrum Disorder: A Capillary Electrophoresis Time-of-Flight Mass Spectroscopy Study
Hitoshi Kuwabara et al.
PLOS ONE (2013)
Fecal Microbiota and Metabolome of Children with Autism and Pervasive Developmental Disorder Not Otherwise Specified
Maria De Angelis et al.
PLOS ONE (2013)
Metabolic changes and DNA hypomethylation in cerebellum are associated with behavioral alterations in mice exposed to trichloroethylene postnatally
Sarah J. Blossom et al.
TOXICOLOGY AND APPLIED PHARMACOLOGY (2013)
Mitochondrial Dysfunction in Autism
Agustin Legido et al.
SEMINARS IN PEDIATRIC NEUROLOGY (2013)
Decreased tryptophan metabolism in patients with autism spectrum disorders
Luigi Boccuto et al.
MOLECULAR AUTISM (2013)
Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism
Eleonora Napoli et al.
MOLECULAR AUTISM (2013)
Complex epigenetic regulation of Engrailed-2 (EN-2) homeobox gene in the autism cerebellum
S. J. James et al.
TRANSLATIONAL PSYCHIATRY (2013)
Redox metabolism abnormalities in autistic children associated with mitochondrial disease
R. E. Frye et al.
TRANSLATIONAL PSYCHIATRY (2013)
Unique acyl-carnitine profiles are potential biomarkers for acquired mitochondrial disease in autism spectrum disorder
R. E. Frye et al.
TRANSLATIONAL PSYCHIATRY (2013)
Alterations in mitochondrial DNA copy number and the activities of electron transport chain complexes and pyruvate dehydrogenase in the frontal cortex from subjects with autism
F. Gu et al.
TRANSLATIONAL PSYCHIATRY (2013)
The link between intraneuronal N-truncated amyloid-β peptide and oxidatively modified lipids in idiopathic autism and dup(15q11.2-q13)/autism
Janusz Frackowiak et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2013)
L-Carnitine supplementation improves the behavioral symptoms in autistic children
Sarah Farid Fahmy et al.
RESEARCH IN AUTISM SPECTRUM DISORDERS (2013)
B-Lymphocytes from a Population of Children with Autism Spectrum Disorder and Their Unaffected Siblings Exhibit Hypersensitivity to Thimerosal
Martyn A. Sharpe et al.
JOURNAL OF TOXICOLOGY (2013)
Toxin Models of Mitochondrial Dysfunction in Parkinson's Disease
Terina N. Martinez et al.
ANTIOXIDANTS & REDOX SIGNALING (2012)
MITOCHONDRIAL DNA MUTATIONS IN TWO BULGARIAN CHILDREN WITH AUTISTIC SPECTRUM DISORDERS
D. Avdjieva-Tzavella et al.
BALKAN JOURNAL OF MEDICAL GENETICS (2012)
Mitochondrial and ion channel gene alterations in autism
Moyra Smith et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2012)
Increased Markers of Oxidative Stress in Autistic Children of the Sultanate of Oman
Musthafa M. Essa et al.
BIOLOGICAL TRACE ELEMENT RESEARCH (2012)
Elevated Fecal Short Chain Fatty Acid and Ammonia Concentrations in Children with Autism Spectrum Disorder
Lv Wang et al.
DIGESTIVE DISEASES AND SCIENCES (2012)
Buccal Swab Analysis of Mitochondrial Enzyme Deficiency and DNA Defects in a Child With Suspected Myoclonic Epilepsy and Ragged Red Fibers (MERRF)
William R. Yorns et al.
JOURNAL OF CHILD NEUROLOGY (2012)
Mitochondrial Disease in 22q13 Duplication Syndrome
Richard E. Frye
JOURNAL OF CHILD NEUROLOGY (2012)
Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism
Ghada A. Abu Shmais et al.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2012)
The enteric bacterial metabolite propionic acid alters brain and plasma phospholipid molecular species: further development of a rodent model of autism spectrum disorders
Raymond H. Thomas et al.
JOURNAL OF NEUROINFLAMMATION (2012)
Non-invasive evaluation of buccal respiratory chain enzyme dysfunction in mitochondrial disease: Comparison with studies in muscle biopsy
Michaell J. Goldenthal et al.
MOLECULAR GENETICS AND METABOLISM (2012)
A review of research trends in physiological abnormalities in autism spectrum disorders: immune dysregulation, inflammation, oxidative stress, mitochondrial dysfunction and environmental toxicant exposures
D. A. Rossignol et al.
MOLECULAR PSYCHIATRY (2012)
Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis
D. A. Rossignol et al.
MOLECULAR PSYCHIATRY (2012)
Genome-wide expression studies in Autism spectrum disorder, Rett syndrome, and Down syndrome
Carla Lintas et al.
NEUROBIOLOGY OF DISEASE (2012)
Brain Region-Specific Glutathione Redox Imbalance in Autism
Abha Chauhan et al.
NEUROCHEMICAL RESEARCH (2012)
1H-MRS in autism spectrum disorders: a systematic meta-analysis
Jonathan C. Ipser et al.
METABOLIC BRAIN DISEASE (2012)
Mitochondrial Dysfunction in Pten Haplo-Insufficient Mice with Social Deficits and Repetitive Behavior: Interplay between Pten and p53
Eleonora Napoli et al.
PLOS ONE (2012)
Brain Transcriptional and Epigenetic Associations with Autism
Matthew R. Ginsberg et al.
PLOS ONE (2012)
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Patricia B. S. Celestino-Soper et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy
Gaia Novarino et al.
SCIENCE (2012)
Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects
Alexa K. Craig et al.
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2012)
Brain region-specific altered expression and association of mitochondria-related genes in autism
Ayyappan Anitha et al.
MOLECULAR AUTISM (2012)
Age-related change in brain metabolite abnormalities in autism: a meta-analysis of proton magnetic resonance spectroscopy studies
Y. Aoki et al.
TRANSLATIONAL PSYCHIATRY (2012)
Evidence of oxidative damage and inflammation associated with low glutathione redox status in the autism brain
S. Rose et al.
TRANSLATIONAL PSYCHIATRY (2012)
Substantial Problems with Measuring Brain Mitochondrial Dysfunction in Autism Spectrum Disorder Using Magnetic Resonance Spectroscopy
Daniel A. Rossignol et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2012)
Further Commentary on Mitochondrial Dysfunction in Autism Spectrum Disorder: Assessment and Treatment Considerations
Stephen R. Dager et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2012)
Metabolic Imbalance Associated with Methylation Dysregulation and Oxidative Damage in Children with Autism
Stepan Melnyk et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2012)
Proton Magnetic Resonance Spectroscopy and MRI Reveal No Evidence for Brain Mitochondrial Dysfunction in Children with Autism Spectrum Disorder
Neva M. Corrigan et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2012)
The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism
T. Marui et al.
ACTA PSYCHIATRICA SCANDINAVICA (2011)
Suggestive evidence on the genetic link between mitochondria dysfunction and autism
Sandra Villafuerte
ACTA PSYCHIATRICA SCANDINAVICA (2011)
Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism
Joachim Hallmayer et al.
ARCHIVES OF GENERAL PSYCHIATRY (2011)
Effects of the enteric bacterial metabolic product propionic acid on object-directed behavior, social behavior, cognition, and neuroinflammation in adolescent rats: Relevance to autism spectrum disorder
Derrick F. MacFabe et al.
BEHAVIOURAL BRAIN RESEARCH (2011)
Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder
Vanesa Alvarez-Iglesias et al.
BMC MEDICAL GENETICS (2011)
Bioenergetic function in cardiovascular cells: The importance of the reserve capacity and its biological regulation
Brian E. Sansbury et al.
CHEMICO-BIOLOGICAL INTERACTIONS (2011)
Assessing bioenergetic function in response to oxidative stress by metabolic profiling
Brian P. Dranka et al.
FREE RADICAL BIOLOGY AND MEDICINE (2011)
Brain region-specific deficit in mitochondrial electron transport chain complexes in children with autism
Abha Chauhan et al.
JOURNAL OF NEUROCHEMISTRY (2011)
Proinflammatory and proapoptotic markers in relation to mono and di-cations in plasma of autistic patients from Saudi Arabia
Afaf K. El-Ansary et al.
JOURNAL OF NEUROINFLAMMATION (2011)
Plasma fatty acids as diagnostic markers in autistic patients from Saudi Arabia
Afaf K. El-Ansary et al.
LIPIDS IN HEALTH AND DISEASE (2011)
A prospective double-blind, randomized clinical trial of levocarnitine to treat autism spectrum disorders
David A. Geier et al.
MEDICAL SCIENCE MONITOR (2011)
Impaired Carbohydrate Digestion and Transport and Mucosal Dysbiosis in the Intestines of Children with Autism and Gastrointestinal Disturbances
Brent L. Williams et al.
PLOS ONE (2011)
Mitochondrial Dysfunction Can Connect the Diverse Medical Symptoms Associated With Autism Spectrum Disorders
Richard E. Frye et al.
PEDIATRIC RESEARCH (2011)
Urinary oxidative stress markers in children with autism
Lakshmi Priya et al.
REDOX REPORT (2011)
MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation
Barbara S. Connolly et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)
Role of cellular bioenergetics in smooth muscle cell proliferation induced by platelet-derived growth factor
Jessica Perez et al.
BIOCHEMICAL JOURNAL (2010)
Regulation of vascular smooth muscle cell bioenergetic function by protein glutathiolation
Bradford G. Hill et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2010)
AUTISM AND MITOCHONDRIAL DISEASE
Richard H. Haas
DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2010)
Expression analyses of the mitochondrial complex I 75-kDa subunit in early onset schizophrenia and autism spectrum disorder: increased levels as a potential biomarker for early onset schizophrenia
Regina Taurines et al.
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY (2010)
Mitochondrial reserve capacity in endothelial cells: The impact of nitric oxide and reactive oxygen species
Brian P. Dranka et al.
FREE RADICAL BIOLOGY AND MEDICINE (2010)
Mitochondrial Dysfunction in Autism
Cecilia Giulivi et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)
Fever Plus Mitochondrial Disease Could Be Risk Factors for Autistic Regression
John Shoffner et al.
JOURNAL OF CHILD NEUROLOGY (2010)
5q14.3 Deletion Manifesting as Mitochondrial Disease and Autism: Case Report
Herbert Ezugha et al.
JOURNAL OF CHILD NEUROLOGY (2010)
Altered brain phospholipid and acylcarnitine profiles in propionic acid infused rodents: further development of a potential model of autism spectrum disorders
Raymond H. Thomas et al.
JOURNAL OF NEUROCHEMISTRY (2010)
Mitochondrial DNA and anti-mitochondrial antibodies in serum of autistic children
Bodi Zhang et al.
JOURNAL OF NEUROINFLAMMATION (2010)
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
L. Palmieri et al.
MOLECULAR PSYCHIATRY (2010)
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility
E. Maestrini et al.
MOLECULAR PSYCHIATRY (2010)
Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan
Wei-Hsien Chien et al.
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY (2010)
Nuclear and Mitochondrial Genome Defects in Autisms
Moyra Smith et al.
YEAR IN HUMAN AND MEDICAL GENETICS 2009 (2009)
Importance of the bioenergetic reserve capacity in response to cardiomyocyte stress induced by 4-hydroxynonenal
Bradford G. Hill et al.
BIOCHEMICAL JOURNAL (2009)
Spare respiratory capacity, oxidative stress and excitotoxicity
David G. Nicholls
BIOCHEMICAL SOCIETY TRANSACTIONS (2009)
Metabolic biomarkers related to energy metabolism in Saudi autistic children
O. A. Al-Mosalem et al.
CLINICAL BIOCHEMISTRY (2009)
Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism
S. Jill James et al.
FASEB JOURNAL (2009)
Utility of Lymphoblastoid Cell Lines
L. Sie et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2009)
Novel plasma phospholipid biomarkers of autism: Mitochondrial dysfunction as a putative causative mechanism
Elodie Pastural et al.
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS (2009)
Autistic spectrum disorders and mitochondrial encephalopathies
David Holtzman
ACTA PAEDIATRICA (2008)
An Analysis of Candidate Autism Loci on Chromosome 2q24-q33: Evidence for Association to the STK39 Gene
Nicolas Ramoz et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism
Jeremy M. Silverman et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene Is Associated With Autism
Joni A. Turunen et al.
AUTISM RESEARCH (2008)
Advances in measuring cellular bioenergetics using extracellular flux
David A. Ferrick et al.
DRUG DISCOVERY TODAY (2008)
Genetics evaluation for the etiologic diagnosis of autism spectrum disorders
G. Bradley Schaefer et al.
GENETICS IN MEDICINE (2008)
The in-depth evaluation of suspected mitochondrial disease
Richard H. Haas et al.
MOLECULAR GENETICS AND METABOLISM (2008)
SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects
A-M Lepagnol-Bestel et al.
MOLECULAR PSYCHIATRY (2008)
Advances in autism genetics: on the threshold of a new neurobiology
Brett S. Abrahams et al.
NATURE REVIEWS GENETICS (2008)
Mitochondrial Disease in Autism Spectrum Disorder Patients: A Cohort Analysis
Jacqueline R. Weissman et al.
PLOS ONE (2008)
An investigation of mitochondrial haplogroups in autism
Lindsey Kent et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Folate receptor autoimmunity and cerebral folate deficiency in low-functioning autism with neurological deficits
V. T. Ramaekers et al.
NEUROPEDIATRICS (2007)
Epidemiology of autism spectrum disorder in Portugal:: prevalence, clinical characterization, and medical conditions
Guiomar Oliveira et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2007)
Autistic disorder in 2 children with mitochondrial disorders
Chang-Yong Tsao et al.
JOURNAL OF CHILD NEUROLOGY (2007)
Spare respiratory capacity rather than oxidative stress regulates glutamate excitotoxicity after partial respiratory inhibition of mitochondrial complex I with rotenone
Nagendra Yadava et al.
JOURNAL OF NEUROSCIENCE (2007)
Aberrant amino acid transport in fibroblasts from children with autism
Elisabeth Fernell et al.
NEUROSCIENCE LETTERS (2007)
Neurobiological effects of intraventricular propionic acid in rats: Possible role of short chain fatty acids on the pathogenesis and characteristics of autism spectrum disorders
Derrick F. MacFabe et al.
BEHAVIOURAL BRAIN RESEARCH (2007)
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome
Erwin Petek et al.
MOLECULAR GENETICS AND GENOMICS (2007)
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism
S. Jill James et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2006)
Mitochondrial disease criteria - Diagnostic applications in children
E. Morava et al.
NEUROLOGY (2006)
Brief report:: High frequency of biochemical markers for mitochondrial dysfunction in autism:: No association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene
Catarina Correia et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2006)
The mitochondrial DNA A3243A>G mutation must be an infrequent cause of Asperger syndrome
Lindsey Kent et al.
JOURNAL OF PEDIATRICS (2006)
Exposure to a metabolite of the environmental toxicant, trichloroethylene, attenuates CD4+ T cell activation-induced cell death by metalloproteinase-dependent FasL shedding
Sarah J. Blossom et al.
TOXICOLOGICAL SCIENCES (2006)
Developmental regression and mitochondrial dysfunction in a child with autism
Jon S. Poling et al.
JOURNAL OF CHILD NEUROLOGY (2006)
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample
F Blasi et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31
R Segurado et al.
AMERICAN JOURNAL OF PSYCHIATRY (2005)
Comparative study of cerebral white matter in autism and attention-deficit/hyperactivity disorder by means of magnetic resonance spectroscopy
N Fayed et al.
ACADEMIC RADIOLOGY (2005)
Mitochondrial dysfunction in autism spectrum disorders:: a population-based study
G Oliveira et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2005)
Linkage and association of the mitochondrial aspartate/ glutamate carrier SLC25A12 gene with autism
N Ramoz et al.
AMERICAN JOURNAL OF PSYCHIATRY (2004)
Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism
SJ James et al.
AMERICAN JOURNAL OF CLINICAL NUTRITION (2004)
Relative carnitine deficiency in autism
PA Filipek et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2004)
Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase
T Clark-Taylor et al.
MEDICAL HYPOTHESES (2004)
Mitochondrial DNA abnormalities and autistic spectrum disorders
R Pons et al.
JOURNAL OF PEDIATRICS (2004)
Reduced folate transport to the CNS in female Rett patients
VT Ramaekers et al.
NEUROLOGY (2003)
Mitochondrial dysfunction in autistic patients with 15q inverted duplication
PA Filipek et al.
ANNALS OF NEUROLOGY (2003)
Asperger syndrome - A proton magnetic resonance spectroscopy study of brain
DGM Murphy et al.
ARCHIVES OF GENERAL PSYCHIATRY (2002)
Gastrointestinal microflora studies in late-onset autism
SM Finegold et al.
CLINICAL INFECTIOUS DISEASES (2002)
Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay:: HEADD syndrome
JJ Filiano et al.
JOURNAL OF CHILD NEUROLOGY (2002)
Clinical spectrum and diagnosis of mitochondrial disorders
A Munnich et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2001)
Autism associated with the mitochondrial DNA G8363A transfer RNALys mutation
WD Graf et al.
JOURNAL OF CHILD NEUROLOGY (2000)
Share Paper
