Oxidative stress in Rett syndrome: Natural history, genotype, and variants

F4-neuroprostanes mediate neurological severity in Rett syndrome

(2011) Cinzia Signorini et al.   CLINICA CHIMICA ACTA

Increased levels of 4HNE-protein plasma adducts in Rett syndrome

(2011) Alessandra Pecorelli et al.   CLINICAL BIOCHEMISTRY

Rett syndrome: Revised diagnostic criteria and nomenclature

(2010) Jeffrey L. Neul et al.   ANNALS OF NEUROLOGY

Reversibility of functional deficits in experimental models of Rett syndrome

(2010) Stuart Cobb et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Downstream targets of methyl CpG binding protein 2 and their abnormal expression in the frontal cortex of the human Rett syndrome brain

(2010) Joanne H Gibson et al.   BMC NEUROSCIENCE

MeCP2270 Mutant Protein Is Expressed in Astrocytes as well as in Neurons and Localizes in the Nucleus

(2010) L.A. Kifayathullah et al.   CYTOGENETIC AND GENOME RESEARCH

Rett Syndrome Microglia Damage Dendrites and Synapses by the Elevated Release of Glutamate

(2010) I. Maezawa et al.   JOURNAL OF NEUROSCIENCE

CDKL5 is a brain MeCP2 target gene regulated by DNA methylation

(2010) Delphine Carouge et al.   NEUROBIOLOGY OF DISEASE

Neurogenetics: Advancing the “Next-Generation” of Brain Research

(2010) Huda Y. Zoghbi et al.   NEURON

Docosahexaenoic Acid Therapy of Experimental Ischemic Stroke

(2010) Ludmila Belayev et al.   Translational Stroke Research

Systemic oxidative stress in classic Rett syndrome

(2009) Claudio De Felice et al.   FREE RADICAL BIOLOGY AND MEDICINE

Oxidative damage in Parkinson disease: Measurement using accurate biomarkers

(2009) Raymond C.S. Seet et al.   FREE RADICAL BIOLOGY AND MEDICINE

Rett Syndrome Astrocytes Are Abnormal and Spread MeCP2 Deficiency through Gap Junctions

(2009) I. Maezawa et al.   JOURNAL OF NEUROSCIENCE

Non–cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

(2009) Nurit Ballas et al.   NATURE NEUROSCIENCE

Understanding Omega-3 Polyunsaturated Fatty Acids

(2009) Philip C. Calder et al.   POSTGRADUATE MEDICINE

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

(2009) Daniela Tropea et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

On the Track of DNA Methylation: An Interview with Adrian Bird

(2009) Jane Gitschier   PLoS Genetics

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

(2008) Francesca Ariani et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)

(2008) A. Renieri et al.   BRAIN & DEVELOPMENT

Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

(2008) J. L. Neul et al.   NEUROLOGY