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scholarly article | Q13442814 |
P50 | author | Martha Herbert | Q15429647 |
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Incidence of minor physical anomaly in autism | Q40078709 | ||
When is the brain enlarged in autism? A meta-analysis of all brain size reports | Q40416498 | ||
Mercury inhibits nitric oxide production but activates proinflammatory cytokine expression in murine macrophage: differential modulation of NF-kappaB and p38 MAPK signaling pathways | Q40711057 | ||
Brain weight in autism: normal in the majority of cases, megalencephalic in rare cases | Q41618863 | ||
Microcephaly and macrocephaly in autism | Q41925681 | ||
What's going on? The question of time trends in autism | Q42338371 | ||
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Prenatal viral infection leads to pyramidal cell atrophy and macrocephaly in adulthood: implications for genesis of autism and schizophrenia | Q44027735 | ||
Hydrogen proton magnetic resonance spectroscopy in autism: preliminary evidence of elevated choline/creatine ratio | Q44043942 | ||
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Rotenone potentiates dopamine neuron loss in animals exposed to lipopolysaccharide prenatally | Q45142314 | ||
Manganese potentiates in vitro production of proinflammatory cytokines and nitric oxide by microglia through a nuclear factor kappa B-dependent mechanism | Q45188778 | ||
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Maternal infection: window on neuroimmune interactions in fetal brain development and mental illness | Q46646904 | ||
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Autism and megalencephaly | Q48285674 | ||
MRI-Based topographic parcellation of human cerebral white matter | Q48299523 | ||
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Neuropathology of infantile autism | Q48418627 | ||
A clinicopathological study of autism | Q48454065 | ||
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Autism and macrocephaly | Q50302422 | ||
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SPECT findings in mentally retarded autistic individuals | Q50312669 | ||
Abnormal ventral temporal cortical activity during face discrimination among individuals with autism and Asperger syndrome | Q50313035 | ||
An MRI study of the corpus callosum and cerebellum in mentally retarded autistic individuals | Q50313469 | ||
White matter structure in autism: preliminary evidence from diffusion tensor imaging | Q50342010 | ||
Brief report: cognitive correlates of enlarged head circumference in children with autism | Q50345108 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | autism | Q38404 |
P304 | page(s) | 417-440 | |
P577 | publication date | 2005-10-01 | |
P1433 | published in | The Neuroscientist | Q7753449 |
P1476 | title | Large brains in autism: the challenge of pervasive abnormality | |
P478 | volume | 11 |
Q34684489 | A model of functional brain connectivity and background noise as a biomarker for cognitive phenotypes: application to autism |
Q48531243 | A simple method for measuring brain asymmetry in children: application to autism. |
Q34316402 | A stable pattern of EEG spectral coherence distinguishes children with autism from neuro-typical controls - a large case control study |
Q37439568 | A voxel-based morphometry comparison of regional gray matter between fragile X syndrome and autism |
Q50310718 | Abnormal functional connectivity in autism spectrum disorders during face processing |
Q93049401 | Abnormal maturation of the resting-state peak alpha frequency in children with autism spectrum disorder |
Q34774073 | Absence of stimulus-driven synchronization effects on sensory perception in autism: Evidence for local underconnectivity? |
Q37201156 | Altered neural connectivity in excitatory and inhibitory cortical circuits in autism. |
Q52331711 | An Inflammation-Centric View of Neurological Disease: Beyond the Neuron. |
Q39240800 | Anthropometric assessment of a Middle Eastern group of autistic children |
Q38052887 | Are ASD and ADHD a Continuum? A Comparison of Pathophysiological Similarities Between the Disorders |
Q50307411 | Are urinary porphyrins a valid diagnostic biomarker of autism spectrum disorder? |
Q36901490 | Atypical functional lateralization of language in autism spectrum disorders |
Q37068738 | Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses |
Q34616361 | Autism, asthma, inflammation, and the hygiene hypothesis |
Q31113873 | Autism: the first firm finding = underconnectivity? |
Q36820898 | Brain region-specific deficit in mitochondrial electron transport chain complexes in children with autism |
Q36474455 | Brain stimulation over Broca's area differentially modulates naming skills in neurotypical adults and individuals with Asperger's syndrome |
Q33825738 | Brain volumetric correlates of autism spectrum disorder symptoms in attention deficit/hyperactivity disorder |
Q50311426 | Brief Report: alterations in cerebral blood flow as assessed by PET/CT in adults with autism spectrum disorder with normal IQ. |
Q57456677 | Cathepsin B inhibition ameliorates leukocyte-endothelial adhesion in the BTBR mouse model of autism |
Q38299791 | Convergence of circuit dysfunction in ASD: a common bridge between diverse genetic and environmental risk factors and common clinical electrophysiology |
Q37396097 | Cortical patterns of category-selective activation for faces, places and objects in adults with autism |
Q38122448 | Developing new pharmacotherapies for autism. |
Q42451941 | Differential effects on white-matter systems in high-functioning autism and Asperger's syndrome. |
Q48574129 | Elevated mean diffusivity in the left hemisphere superior longitudinal fasciculus in autism spectrum disorders increases with more profound language impairment |
Q48452547 | Emergence of layer IV barrel cytoarchitecture is delayed in somatosensory cortex of GAP-43 deficient mice following delayed development of dendritic asymmetry |
Q36470335 | Evidence of microglial activation in autism and its possible role in brain underconnectivity |
Q49090632 | Fronto-temporal disconnectivity and symptom severity in children with autism spectrum disorder |
Q22337413 | Genetic disorders associated with macrocephaly |
Q33740525 | Gestational Exposure to Air Pollution Alters Cortical Volume, Microglial Morphology, and Microglia-Neuron Interactions in a Sex-Specific Manner |
Q30488414 | Growth-related neural reorganization and the autism phenotype: a test of the hypothesis that altered brain growth leads to altered connectivity |
Q37067469 | Head circumferences in twins with and without Autism Spectrum Disorders |
Q89859472 | Increased hippocampal shape asymmetry and volumetric ventricular asymmetry in autism spectrum disorder |
Q34373491 | Inflectional morphology in high-functioning autism: Evidence for speeded grammatical processing |
Q42779521 | Information gain in the brain's resting state: A new perspective on autism |
Q64084484 | Interaction of glutathione S-transferase polymorphisms and tobacco smoking during pregnancy in susceptibility to autism spectrum disorders |
Q38434299 | Learning and consolidation of new spoken words in autism spectrum disorder |
Q35130700 | Left-hemispheric microstructural abnormalities in children with high-functioning autism spectrum disorder |
Q22251256 | Mapping Early Brain Development in Autism |
Q37464235 | Mapping brain abnormalities in boys with autism |
Q34533739 | Maternal inflammation contributes to brain overgrowth and autism-associated behaviors through altered redox signaling in stem and progenitor cells |
Q42062971 | Modeling autism: a systems biology approach |
Q37623381 | Neuro-immune abnormalities in autism and their relationship with the environment: a variable insult model for autism. |
Q48446412 | Neuroanatomical differences in brain areas implicated in perceptual and other core features of autism revealed by cortical thickness analysis and voxel-based morphometry |
Q38178104 | Neuroimaging in autism--from basic science to translational research |
Q28505855 | Neuroligins determine synapse maturation and function |
Q22251205 | New Developments in Autism |
Q64059020 | Novel Contribution of Secreted Amyloid-β Precursor Protein to White Matter Brain Enlargement in Autism Spectrum Disorder |
Q33579948 | Power law scaling in synchronization of brain signals depends on cognitive load |
Q28285118 | Psychosis and autism as diametrical disorders of the social brain |
Q35695272 | Quantitative temporal lobe differences: autism distinguished from controls using classification and regression tree analysis |
Q34027121 | Reduced gyral window and corpus callosum size in autism: possible macroscopic correlates of a minicolumnopathy |
Q33266464 | Regional gray matter volumetric changes in autism associated with social and repetitive behavior symptoms |
Q26772834 | Relevance of Neuroinflammation and Encephalitis in Autism |
Q34288000 | Resistance to change and vulnerability to stress: autistic-like features of GAP43-deficient mice. |
Q96953395 | Role of Neuroinflammation in Autism Spectrum Disorder and the Emergence of Brain Histaminergic System. Lessons Also for BPSD? |
Q30491598 | Shared and idiosyncratic cortical activation patterns in autism revealed under continuous real-life viewing conditions. |
Q36327061 | Sociability and brain development in BALB/cJ and C57BL/6J mice |
Q58780865 | Social Skills Deficits in Autism Spectrum Disorder: Potential Biological Origins and Progress in Developing Therapeutic Agents |
Q30582661 | Structural connectivity and diffusion tensor imaging in autism spectrum disorders |
Q91249357 | Systemic treatment with the enteric bacterial metabolic product propionic acid results in reduction of social behavior in juvenile rats: Contribution to a rodent model of autism spectrum disorder |
Q24553624 | The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autism |
Q41809670 | The cellular response in neuroinflammation: The role of leukocytes, microglia and astrocytes in neuronal death and survival. |
Q34699035 | The neurobiology of autism |
Q37090091 | The relation between connection length and degree of connectivity in young adults: a DTI analysis |
Q30494180 | Vibrotactile adaptation fails to enhance spatial localization in adults with autism |
Q35695225 | Volumetric and voxel-based morphometry findings in autism subjects with and without macrocephaly |
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