about
Brain functional networks in syndromic and non-syndromic autism: a graph theoretical study of EEG connectivity.EphB-mediated degradation of the RhoA GEF Ephexin5 relieves a developmental brake on excitatory synapse formationPromoting axon regeneration in the adult CNS by modulation of the PTEN/mTOR pathwayHuman CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndromeEpileptogenesis in neurocutaneous disorders with focus in Sturge Weber syndromeGenes, circuits, and precision therapies for autism and related neurodevelopmental disordersThe neurology of mTORPediatric epileptologyEph-dependent tyrosine phosphorylation of ephexin1 modulates growth cone collapseHomozygous PLCB1 deletion associated with malignant migrating partial seizures in infancyThe neuroprotective drug riluzole acts via small conductance Ca2+-activated K+ channels to ameliorate defects in spinal muscular atrophy modelsA mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survivalNeuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1Cdk5 regulates EphA4-mediated dendritic spine retraction through an ephexin1-dependent mechanismTuberous sclerosis complex proteins control axon formationBoth maternal and pup genotype influence ultrasonic vocalizations and early developmental milestones in tsc2 (+/-) mice.Prenatal rapamycin results in early and late behavioral abnormalities in wildtype C57BL/6 miceA mathematical framework for the registration and analysis of multi-fascicle models for population studies of the brain microstructure.Mechanism-based treatment in tuberous sclerosis complex.Diffusion tensor imaging and related techniques in tuberous sclerosis complex: review and future directions.Cerebellar Development and Autism Spectrum Disorder in Tuberous Sclerosis Complex.Sturge-Weber Syndrome: Brain Magnetic Resonance Imaging and Neuropathology Findings.Neonatal subependymal giant cell astrocytoma: new case and review of literature.Clinical presentation and diagnosis of tuberous sclerosis complex in infancy.Diffusion features of white matter in tuberous sclerosis with tractographyATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROSVisual Evoked Potentials as a Readout of Cortical Function in Infants With Tuberous Sclerosis Complex.Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism.Autism spectrum disorder and epileptic encephalopathy: common causes, many questions.RASA1 functions in EPHB4 signaling pathway to suppress endothelial mTORC1 activity.Leveraging a Sturge-Weber Gene Discovery: An Agenda for Future Research.The syndrome of perisylvian polymicrogyria with congenital arthrogryposis.Early developmental trajectories associated with ASD in infants with tuberous sclerosis complex.Expression of PTPH1, a rat protein tyrosine phosphatase, is restricted to the derivatives of a specific diencephalic segment.NMDA mediated contextual conditioning changes miRNA expressionFebrile infection-related epilepsy syndrome (FIRES): pathogenesis, treatment, and outcome: a multicenter study on 77 children.Murine Glut-1 transporter haploinsufficiency: postnatal deceleration of brain weight and reactive astrocytosis.SMN regulates axonal local translation via miR-183/mTOR pathwaySomatic mutations in cerebral cortical malformations.Regulable neural progenitor-specific Tsc1 loss yields giant cells with organellar dysfunction in a model of tuberous sclerosis complex.
P50
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