Infantile tauopathies: Hemimegalencephaly; tuberous sclerosis complex; focal cortical dysplasia 2; ganglioglioma
- 1 June 2015
- journal article
- review article
- Published by Elsevier BV in Brain & Development
- Vol. 37 (6), 553-562
- https://doi.org/10.1016/j.braindev.2014.08.010
Abstract
No abstract availableKeywords
This publication has 97 references indexed in Scilit:
- Simultaneous analysis of cerebrospinal fluid biomarkers using microsphere-based xMAP multiplex technology for early detection of Alzheimer’s diseaseMethods, 2012
- Somatic Activation of AKT3 Causes Hemispheric Developmental Brain MalformationsNeuron, 2012
- Acetylated tau, a novel pathological signature in Alzheimer's disease and other tauopathiesBrain, 2012
- Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndromeGenes, Brain and Behavior, 2012
- Hyperphosphorylated tau in young and middle-aged subjectsActa Neuropathologica, 2011
- A Mosaic Activating Mutation inAKT1Associated with the Proteus SyndromeThe New England Journal of Medicine, 2011
- Selective pharmacogenetic inhibition of mammalian target of Rapamycin complex I (mTORC1) blocks long-term synaptic plasticity and memory storageProceedings of the National Academy of Sciences of the United States of America, 2011
- The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1Epilepsia, 2010
- Comparative study of cellular and synaptic abnormalities in brain tissue samples from pediatric tuberous sclerosis complex and cortical dysplasia type IIEpilepsia, 2010
- Mechanisms of tau-induced neurodegenerationActa Neuropathologica, 2009