Volume 125, Issue 3, March 2013

ISSN: 0001-6322 (Print) 1432-0533 (Online)

In this issue (14 articles)

  1. Editorial

    Polymorphonuclear neutrophil infiltration into ischemic infarctions: myth or truth?

    Hannu Kalimo, Gregory J. del Zoppo, Anders Paetau… Pages 313-316
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    Review

    Evolving neurobiology of tuberous sclerosis complex

    Peter B. Crino Pages 317-332
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    Review

    Nervous system involvement in von Hippel–Lindau disease: pathology and mechanisms

    Alexander O. Vortmeyer, Eric A. Falke, Sven Gläsker, Jie Li… Pages 333-350
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    Original Paper

    Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations

    David E. Reuss, Rosario M. Piro, David T. W. Jones, Matthias Simon… Pages 351-358
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    Original Paper

    DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies

    Edward C. Schwalbe, Daniel Williamson, Janet C. Lindsey… Pages 359-371
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    Original Paper

    Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastoma

    Adrian M. Dubuc, Marc Remke, Andrey Korshunov, Paul A. Northcott… Pages 373-384
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    Original Paper

    OTX2 sustains a bivalent-like state of OTX2-bound promoters in medulloblastoma by maintaining their H3K27me3 levels

    Jens Bunt, Nancy A. Hasselt, Danny A. Zwijnenburg, Jan Koster… Pages 385-394
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  8. Original Paper

    The neurovascular unit as a selective barrier to polymorphonuclear granulocyte (PMN) infiltration into the brain after ischemic injury

    Gaby Enzmann, Caroline Mysiorek, Roser Gorina, Yu-Jung Cheng… Pages 395-412
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    Original Paper

    hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

    Kohji Mori, Sven Lammich, Ian R. A. Mackenzie, Ignasi Forné… Pages 413-423
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    Original Paper

    Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia

    Shinsuke Fujioka, Christina Sundal, Audrey J. Strongosky… Pages 425-438
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    Original Paper

    VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy

    Nivetha Ramachandran, Iulia Munteanu, Peixiang Wang… Pages 439-457
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    Correspondence

    Lysosomal storage and advanced senescence in the brain of LAMP-2-deficient Danon disease

    Akiko Furuta, Koichi Wakabayashi, Joji Haratake, Hisae Kikuchi… Pages 459-461
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    Correspondence

    Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid

    Eileen H. Bigio, Jane Y. Wu, Han-Xiang Deng, Esther N. Bit-Ivan… Pages 463-465
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  14. Erratum

    Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38

    Maria Luisa Moro, Giorgio Giaccone, Raffaella Lombardi… Page 467
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