Original Paper
Online First™Cytoarchitectural alterations are widespread in cerebral cortex in tuberous sclerosis complex
Leah Marcotte, Eleonora Aronica, Marianna Baybis and Peter B. Crino
Online First™, 10 February 2012
Review
Online First™Primary progressive multiple sclerosis: part of the MS disease spectrum or separate disease entity?
Jack Antel, Samson Antel, Zografos Caramanos, Douglas L. Arnold and Tanja Kuhlmann
Online First™, 10 February 2012
Original Paper
Online First™A prognostic gene expression signature in infratentorial ependymoma
Khalida Wani, Terri S. Armstrong, Elizabeth Vera-Bolanos, Aditya Raghunathan and David Ellison, et al.
Online First™, 9 February 2012
Review
Online First™Commensal gut flora and brain autoimmunity: a love or hate affair?
Kerstin Berer and Gurumoorthy Krishnamoorthy
Online First™, 9 February 2012
Correspondence
Online First™Optineurin immunoreactivity in neuronal nuclear inclusions of polyglutamine diseases (Huntington’s, DRPLA, SCA2, SCA3) and intranuclear inclusion body disease
Fumiaki Mori, Kunikazu Tanji, Yasuko Toyoshima, Mari Yoshida and Akiyoshi Kakita, et al.
Online First™, 8 February 2012
Editorial
Online First™Peripheral nerve sheath tumors: the elegant chapter in surgical neuropathology
Fausto J. Rodriguez
Online First™, 7 February 2012
Original Paper
Online First™Open AccessCD105 (Endoglin) exerts prognostic effects via its role in the microvascular niche of paediatric high grade glioma
Stuart J. Smith, Hanna Tilly, Jennifer H. Ward, Donald C. Macarthur and James Lowe, et al.
Online First™, 7 February 2012
Correspondence
Online First™GNAQ and GNA11 mutations in melanocytomas of the central nervous system
Rajmohan Murali, Thomas Wiesner, Marc K. Rosenblum and Boris C. Bastian
Online First™, 3 February 2012
Original Paper
Online First™An essential role for p38 MAPK in cerebellar granule neuron precursor proliferation
Cemile G. Guldal, Adiba Ahmad, Andrey Korshunov, Massimo Squatrito and Aashir Awan, et al.
Online First™, 2 February 2012
Case Reports
Online First™TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation
Maria Martinez-Lage, Laura Molina-Porcel, Dana Falcone, Leo McCluskey and Virginia M.-Y. Lee, et al.
Online First™, 2 February 2012