Review articleTuberous sclerosis complex: a review of neurological aspects
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Concurrent diagnoses of Tuberous sclerosis and multiple sclerosis
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2020, Annals of Medicine and SurgeryNeuron-Glia Interactions Increase Neuronal Phenotypes in Tuberous Sclerosis Complex Patient iPSC-Derived Models
2019, Stem Cell ReportsCitation Excerpt :Tuberous sclerosis complex (TSC) is a rare genetic, neurodevelopmental disorder, which affects multiple organs (Leung and Robson, 2007), causing benign tumors in the brain, eyes, heart, lung, liver, kidney, and skin. The neuropathological features in the brain involve cortical tubers and subependymal nodules (Curatolo et al., 2002). Many studies also indicate glial-associated phenotypes, including giant astrocytoma (Beaumont et al., 2015) and white matter abnormalities (Curatolo et al., 2002; Marti-Bonmati et al., 2000).
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Correspondence: Paolo Curatolo, Paediatric Neurology, Department of Neurosciences, Via di Tor Vergata 135, 00133 Rome, Italy Fax:: +39.06.9411463. e-mail:[email protected]
Copyright © 2002 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.