Myelin Pathology Beyond White Matter in Tuberous Sclerosis Complex (TSC) Cortical Tubers

Abstract Tuberous sclerosis complex (TSC) is a monogenetic disease that arises due to mutations in either the TSC1 or TSC2 gene and affects multiple organ systems. One of the hallmark manifestations of TSC are cortical malformations referred to as cortical tubers. These tubers are frequently associa...

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Veröffentlicht in:	Journal of neuropathology and experimental neurology 2020-10, Vol.79 (10), p.1054-1064
Hauptverfasser:	Mühlebner, Angelika, van Scheppingen, Jackelien, de Neef, Andrew, Bongaarts, Anika, Zimmer, Till S, Mills, James D, Jansen, Floor E, Spliet, Wim G M, Krsek, Pavel, Zamecnik, Josef, Coras, Roland, Blumcke, Ingmar, Feucht, Martha, Scholl, Theresa, Gruber, Victoria-Elisabeth, Hainfellner, Johannes A, Söylemezoğlu, Figen, Kotulska, Katarzyna, Lagae, Lieven, Jansen, Anna C, Kwiatkowski, David J, Jozwiak, Sergiusz, Curatolo, Paolo, Aronica, Eleonora
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities Brain Cerebral Cortex - pathology Cognition disorders Complications and side effects Female Genetic aspects Gray Matter - pathology Health aspects Humans Male Myelin proteins Myelin Sheath - pathology Oligodendroglia - pathology Original Risk factors Tuberous sclerosis Tuberous Sclerosis - pathology White Matter - pathology
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