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Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

http://www.wikidata.org/entity/Q37178721

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Recent advances in understanding synaptic abnormalities in Rett syndrome Rett syndrome and other autism spectrum disorders--brain diseases of immune malfunction?Twenty-four hour quantitative-EEG and in-vivo glutamate biosensor detects activity and circadian rhythm dependent biomarkers of pathogenesis in Mecp2 null mice.Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice.Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndrome Microglial dysregulation in psychiatric disease Selective impact of MeCP2 and associated histone deacetylases on the dynamics of evoked excitatory neurotransmission Education of a child neurologist: developmental neuroscience relevant to child neurology.Deficient Purposeful Use of Forepaws in Female Mice Modelling Rett Syndrome.Correlation of the vesicular acetylcholine transporter densities in the striata to the clinical abilities of women with Rett syndrome.Enhancement of postsynaptic GABAA and extrasynaptic NMDA receptor-mediated responses in the barrel cortex of Mecp2-null mice.High Glucose-Induced PC12 Cell Death by Increasing Glutamate Production and Decreasing Methyl Group Metabolism.Does microglial dysfunction play a role in autism and Rett syndrome?Neurobiologically-based treatments in Rett syndrome: opportunities and challenges.The role of oxidative stress in Rett syndrome: an overview.Genetic control of postnatal human brain growth.Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate.Dysregulation of glutamine transporter SNAT1 in Rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicity.Altered carbon dioxide metabolism and creatine abnormalities in rett syndrome.Dendrimer-mediated delivery of N-acetyl cysteine to microglia in a mouse model of Rett syndrome.Social impairments in Rett syndrome: characteristics and relationship with clinical severity.

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Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

http://www.wikidata.org/entity/Q37178721

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

@en

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

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type

label

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

@en

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

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prefLabel

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

@en

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

@nl

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Annals of Neurology

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Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.

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Alena Horská

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Genila Bibat

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Luciano Farage

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Lídia M Nagae

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Peter B Barker

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SakkuBai Naidu

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Walter E Kaufmann

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P2860

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively

Neuroimaging studies in Rett syndrome.

Proton MR spectroscopy in Rett syndrome.

Relationships between astrogliosis and 1H MR spectroscopic measures of brain choline/creatine and myo-inositol/creatine in a primate model.

Genotype and early development in Rett syndrome: the value of international data.

Investigating genotype-phenotype relationships in Rett syndrome using an international data set.

Development of amino acid receptors in frontal cortex from girls with Rett syndrome.

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.

Rett Syndrome -- an update.

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90-97

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scholarly article

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10.1002/ANA.21562

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1

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65

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2009-01-01T00:00:00Z

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23981282

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19194883

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2676876

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