Neuronal migration disorders: clinical, neuroradiologic and genetics aspects (original) (raw)

Recent Development in Neuronal Migration Disorders: Clinical, Neuroradiologic and Genetics Aspects

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Current Pediatric Reviews, 2008

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New trends in neuronal migration disorders

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X-linked malformations of neuronal migration

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Neuronal migration disorders: from genetic diseases to developmental mechanisms

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Clinical patterns of neuronal migrational disorders and parental consanguinity

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Journal of Tropical Pediatrics

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Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain

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Human Molecular Genetics, 1997

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Genes that regulate neuronal migration in the cerebral cortex

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Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders

Walter Silva

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Lissencephalic syndromes: brain and beyond

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Neuronal Migration Disorder – a Clinical Case

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Romanian Journal of Pediatrics, 2015

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Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patients

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Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular Heterotopia

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Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder

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Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly

Gaëlle Friocourt

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Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration

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Malformations of Cortical Development

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Two reciprocal translocations associated with microcephaly and retardation

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A genetic animal model of human neocortical heterotopia associated with seizures

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Responsible Genes for Neuronal Migration in the Chromosome 17p13.3: Beyond Pafah1b1(Lis1), Crk and Ywhae(14-3-3ε

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Why Malformations of Cortical Development Cause Epilepsy

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Inborn Errors of Metabolism leading to Neuronal Migration Defects

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Epileptogenic malformations of cortical development: when evolution goes awry

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Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III

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SCN2A mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders

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Periventricular Heterotopia and the Genetics of Neuronal Migration in the Cerebral Cortex

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The American Journal of Human Genetics, 1999

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What disorders of cortical development tell us about the cortex: one plus one does not always make two

Chiara Manzini

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Epilepsy and malformations of the cerebral cortex

Federico Sicca

2003

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Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different

Jelena Martinovic

American Journal of Medical Genetics, 2004

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