Pages that link to "Q26858999"
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The following pages link to A developmental and genetic classification for malformations of cortical development: update 2012 (Q26858999):
Displaying 50 items.
- Expression Analysis Highlights AXL as a Candidate Zika Virus Entry Receptor in Neural Stem Cells (Q23670968) (← links)
- RTTN mutations link primary cilia function to organization of the human cerebral cortex (Q24297843) (← links)
- Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human (Q24298230) (← links)
- Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures (Q24339517) (← links)
- Comparative Analysis Between Flaviviruses Reveals Specific Neural Stem Cell Tropism for Zika Virus in the Mouse Developing Neocortex (Q26252479) (← links)
- Severe NDE1-mediated microcephaly results from neural progenitor cell cycle arrests at multiple specific stages (Q26690500) (← links)
- Computational analysis in epilepsy neuroimaging: A survey of features and methods (Q26750063) (← links)
- Cerebral cortex expansion and folding: what have we learned? (Q26750873) (← links)
- Diagnostic techniques to detect the epileptogenic zone: Pathophysiological and presurgical analysis of epilepsy in dogs and cats (Q26751100) (← links)
- Malformations of cortical development: 3T magnetic resonance imaging features (Q26777850) (← links)
- Genes and brain malformations associated with abnormal neuron positioning (Q26779045) (← links)
- Physical biology of human brain development (Q26798978) (← links)
- Hemispherectomy in the treatment of seizures: a review (Q26825778) (← links)
- Epilepsy related to developmental tumors and malformations of cortical development (Q26829946) (← links)
- Extracellular and Intracellular Signaling for Neuronal Polarity (Q27005889) (← links)
- A restricted period for formation of outer subventricular zone defined by Cdh1 and Trnp1 levels (Q27314071) (← links)
- Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression (Q27322815) (← links)
- Whole-brain MRI phenotyping in dysplasia-related frontal lobe epilepsy. (Q27348629) (← links)
- The surgically remediable syndrome of epilepsy associated with bottom-of-sulcus dysplasia. (Q27349155) (← links)
- Editorial brain malformation surveillance in the Zika era (Q27927969) (← links)
- Genetic Basis of Brain Malformations (Q28076998) (← links)
- Diagnostic methods and treatment options for focal cortical dysplasia (Q28081144) (← links)
- Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly (Q28281096) (← links)
- Interleukin-1 beta guides the migration of cortical neurons (Q28575658) (← links)
- Molecular and cellular insights into Zika virus-related neuropathies (Q28577785) (← links)
- Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene (Q28581093) (← links)
- Coevolution of radial glial cells and the cerebral cortex (Q28596452) (← links)
- Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamics (Q28973590) (← links)
- Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project (Q30411527) (← links)
- Pacemaker GABA synaptic activity may contribute to network synchronization in pediatric cortical dysplasia (Q30561131) (← links)
- Midline brain-in-brain malformation associated with bilateral perirolandic cortical abnormalities: an image review of this rare disorder (Q30570667) (← links)
- Dampened hippocampal oscillations and enhanced spindle activity in an asymptomatic model of developmental cortical malformations (Q30576703) (← links)
- Layer-specific gene expression in epileptogenic type II focal cortical dysplasia: normal-looking neurons reveal the presence of a hidden laminar organization (Q30578289) (← links)
- Automated detection of cortical dysplasia type II in MRI-negative epilepsy (Q30585191) (← links)
- Leading-process actomyosin coordinates organelle positioning and adhesion receptor dynamics in radially migrating cerebellar granule neurons (Q30614200) (← links)
- De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly (Q30647055) (← links)
- Intrinsic epileptogenicity of dysplastic cortex: converging data from experimental models and human patients. (Q30664740) (← links)
- TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis (Q30670235) (← links)
- Brain malformations and mutations in α- and β-tubulin genes: a review of the literature and description of two new cases. (Q30726699) (← links)
- The genetics of lissencephaly (Q30826834) (← links)
- Polymicrogyria: a common and heterogeneous malformation of cortical development (Q30828370) (← links)
- Functional network alterations and their structural substrate in drug-resistant epilepsy (Q30883108) (← links)
- Cortical abnormalities on MRI: what a neurologist should know (Q30940326) (← links)
- Dysplastic Cerebellar Epilepsy: Complete Seizure Control Following Resection of a Ganglioglioma (Q30982503) (← links)
- MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendations (Q31109389) (← links)
- Malformations of Cortical Development: From Postnatal to Fetal Imaging (Q31133197) (← links)
- Surgery for epileptogenic cerebral dysplasia in children (Q31136189) (← links)
- The Prevalence of Malformations of Cortical Development in a Pediatric Hereditary Hemorrhagic Telangiectasia Population. (Q31153252) (← links)
- Malformations of cortical development: genetic mechanisms and diagnostic approach (Q31162335) (← links)
- PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment (Q32884505) (← links)