Published in Biochem Biophys Res Commun on December 20, 2005
Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology. Nat Neurosci (2009) 3.42
Modulation of RhoGTPases improves the behavioral phenotype and reverses astrocytic deficits in a mouse model of Rett syndrome. Neuropsychopharmacology (2011) 1.09
Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model. PLoS One (2007) 1.06
Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity. Mol Psychiatry (2014) 1.04
Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndrome. PLoS One (2012) 0.96
Developmental and maintenance defects in Rett syndrome neurons identified by a new mouse staging system in vitro. Front Cell Neurosci (2014) 0.92
Evolution of extra-nigral damage predicts behavioural deficits in a rat proteasome inhibitor model of Parkinson's disease. PLoS One (2011) 0.92
Brain metabolism in Rett syndrome: age, clinical, and genotype correlations. Ann Neurol (2009) 0.92
Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice. Anat Rec (Hoboken) (2011) 0.91
Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism. Neurotherapeutics (2015) 0.91
Astrocytes conspire with neurons during progression of neurological disease. Curr Opin Neurobiol (2012) 0.90
Does the effectiveness of the ketogenic diet in different epilepsies yield insights into its mechanisms? Epilepsia (2008) 0.84
Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patients. Mediators Inflamm (2013) 0.79
Long-term home cage activity scans reveal lowered exploratory behaviour in symptomatic female Rett mice. Behav Brain Res (2013) 0.77
Neuroimaging endophenotypes in animal models of autism spectrum disorders: lost or found in translation? Psychopharmacology (Berl) (2013) 0.75
Mitochondrial Dysfunction in the Pathogenesis of Rett Syndrome: Implications for Mitochondria-Targeted Therapies. Front Cell Neurosci (2017) 0.75
Alterations in the carnitine cycle in a mouse model of Rett syndrome. Sci Rep (2017) 0.75
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet (2010) 3.82
Do oxidative and anaerobic energy production in exercising muscle change throughout growth and maturation? J Appl Physiol (1985) (2010) 3.29
Decreased basal fMRI functional connectivity in epileptogenic networks and contralateral compensatory mechanisms. Hum Brain Mapp (2009) 2.38
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice. J Neurosci (2005) 2.20
Graph theoretical analysis of structural and functional connectivity MRI in normal and pathological brain networks. MAGMA (2010) 1.75
Experience of diffusion tensor imaging and 1H spectroscopy for outcome prediction in severe traumatic brain injury: Preliminary results. Crit Care Med (2009) 1.69
Multiminicore disease in a family susceptible to malignant hyperthermia: histology, in vitro contracture tests, and genetic characterization. Arch Neurol (2004) 1.65
Role of resting state functional connectivity MRI in presurgical investigation of mesial temporal lobe epilepsy. J Neurol Neurosurg Psychiatry (2010) 1.47
Imaging experimental cerebral malaria in vivo: significant role of ischemic brain edema. J Neurosci (2005) 1.45
Non-invasive diagnostic of cardiac allograft vasculopathy by 31P magnetic resonance chemical shift imaging. Eur J Cardiothorac Surg (2005) 1.41
NOS substrate during cardioplegic arrest and cold storage decreases stunning after heart transplantation in a rat model. J Heart Lung Transplant (2003) 1.39
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. Brain (2010) 1.30
Myocardial blood flow mapping in mice using high-resolution spin labeling magnetic resonance imaging: influence of ketamine/xylazine and isoflurane anesthesia. Magn Reson Med (2005) 1.25
Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome. Eur J Neurosci (2007) 1.23
Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients. Hum Mol Genet (2002) 1.20
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations. Epilepsia (2011) 1.18
Atrophy mainly affects the limbic system and the deep grey matter at the first stage of multiple sclerosis. J Neurol Neurosurg Psychiatry (2010) 1.18
Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancy. Hum Mutat (2013) 1.13
Comparative MRI analysis of T2 changes associated with single and repeated bouts of downhill running leading to eccentric-induced muscle damage. J Appl Physiol (1985) (2008) 1.11
Reproducibility assessment of metabolic variables characterizing muscle energetics in vivo: A 31P-MRS study. Magn Reson Med (2009) 1.11
Interictal functional connectivity of human epileptic networks assessed by intracerebral EEG and BOLD signal fluctuations. PLoS One (2011) 1.09
The incidence of Rett syndrome in France. Pediatr Neurol (2006) 1.09
Grid-free interactive and automated data processing for MR chemical shift imaging data. MAGMA (2009) 1.09
Effect of maturation on the relationship between muscle size and force production. Med Sci Sports Exerc (2008) 1.08
Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype. Eur J Hum Genet (2010) 1.08
Compensatory cortical activation observed by fMRI during a cognitive task at the earliest stage of MS. Hum Brain Mapp (2003) 1.07
Magnetic resonance spectroscopy reveals an impaired brain metabolic profile in mice resistant to cerebral malaria infected with Plasmodium berghei ANKA. J Biol Chem (2007) 1.06
Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice. J Neurosci Res (2010) 1.06
Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model. PLoS One (2007) 1.06
In vivo pH in metabolic-defective Ras-transformed fibroblast tumors: key role of the monocarboxylate transporter, MCT4, for inducing an alkaline intracellular pH. Int J Cancer (2011) 1.05
High-resolution myocardial perfusion mapping in small animals in vivo by spin-labeling gradient-echo imaging. Magn Reson Med (2004) 1.04
Perfusional deficit and the dynamics of cerebral edemas in experimental traumatic brain injury using perfusion and diffusion-weighted magnetic resonance imaging. J Neurotrauma (2007) 1.04
Structure of WM bundles constituting the working memory system in early multiple sclerosis: a quantitative DTI tractography study. Neuroimage (2007) 1.04
The rate of PCr resynthesis is not a reliable index of skeletal muscle oxidative capacity. Eur J Appl Physiol (2013) 1.04
A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype. Hum Mutat (2007) 1.04
Heterogeneity of muscle recruitment pattern during pedaling in professional road cyclists: a magnetic resonance imaging and electromyography study. Eur J Appl Physiol (2004) 1.02
(1)H MR spectroscopy of human brain tumours: a practical approach. Eur J Radiol (2008) 1.02
Functional magnetic resonance imaging and cognition at the very early stage of MS. J Neurol Sci (2006) 1.01
Assessing brain connectivity at rest is clinically relevant in early multiple sclerosis. Mult Scler (2012) 1.00
Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse. Neurobiol Dis (2010) 1.00
Use of proton magnetic resonance spectroscopy of the brain to differentiate gliomatosis cerebri from low-grade glioma. J Neurosurg (2003) 0.99
Magnetic resonance study of the influence of tissue damage and cortical reorganization on PASAT performance at the earliest stage of multiple sclerosis. Hum Brain Mapp (2005) 0.99
Inflammatory multiple-sclerosis plaques generate characteristic metabolic profiles in cerebrospinal fluid. PLoS One (2007) 0.99
Pathophysiology and clinical presentations of rhabdomyolysis. Joint Bone Spine (2005) 0.99
Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia. J Med Genet (2009) 0.97
Truncation of NHEJ1 in a patient with polymicrogyria. Hum Mutat (2007) 0.97
Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse. Neurosci Lett (2008) 0.97
MRS of normal and impaired fetal brain development. Eur J Radiol (2006) 0.97
In vivo assessment of myocardial blood flow in rat heart using magnetic resonance imaging: effect of anesthesia. J Magn Reson Imaging (2005) 0.97
TCF4 deletions in Pitt-Hopkins Syndrome. Hum Mutat (2008) 0.96
Basal functional connectivity within the anterior temporal network is associated with performance on declarative memory tasks. Neuroimage (2011) 0.95
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. Orphanet J Rare Dis (2013) 0.94
Noninvasive diagnostic assessment of brain tumors using combined in vivo MR imaging and spectroscopy. Magn Reson Med (2006) 0.94
Voxel-based analysis of MTR images: a method to locate gray matter abnormalities in patients at the earliest stage of multiple sclerosis. J Magn Reson Imaging (2004) 0.94
Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain. BMC Neurosci (2011) 0.93
Melanin-concentrating hormone regulates beat frequency of ependymal cilia and ventricular volume. Nat Neurosci (2013) 0.92
Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling. Eur J Hum Genet (2002) 0.92
Value of in vivo T2 measurement for myocardial fibrosis assessment in diabetic mice at 11.75 T. Invest Radiol (2012) 0.92
Is high-frequency neuromuscular electrical stimulation a suitable tool for muscle performance improvement in both healthy humans and athletes? Eur J Appl Physiol (2011) 0.92
Comparative analysis of skeletal muscle oxidative capacity in children and adults: a 31P-MRS study. Appl Physiol Nutr Metab (2008) 0.92
White matter maturation of normal human fetal brain. An in vivo diffusion tensor tractography study. Brain Behav (2011) 0.92
Epilepsy in Rett syndrome--lessons from the Rett networked database. Epilepsia (2015) 0.90
Altered functional connectivity related to white matter changes inside the working memory network at the very early stage of MS. J Cereb Blood Flow Metab (2005) 0.90
Effects of medial temporal lobe degeneration on brain perfusion in amnestic MCI of AD type: deafferentation and functional compensation? Eur J Nucl Med Mol Imaging (2009) 0.90
Progressive motor and respiratory metabolism deficits in post-weaning Mecp2-null male mice. Behav Brain Res (2010) 0.89
Relationships between gray matter metabolic abnormalities and white matter inflammation in patients at the very early stage of MS : a MRSI study. J Neurol (2007) 0.89
Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway. Neurobiol Dis (2011) 0.89
Functional connectivity changes differ in early and late-onset Alzheimer's disease. Hum Brain Mapp (2013) 0.89