C9ORF72, the new gene on the block, causes C9FTD/ALS: new insights provided by neuropathology Eileen H. Bigio Editorial 20 November 2011 Pages: 653 - 655
Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology Paul G. InceJ. Robin HighleyPamela J. Shaw Review 22 November 2011 Pages: 657 - 671
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 Melissa E. MurrayMariely DeJesus-HernandezDennis W. Dickson Original Paper 15 November 2011 Pages: 673 - 690
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS Safa Al-SarrajAndrew KingChristopher E. Shaw Original Paper 19 November 2011 Pages: 691 - 702
TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype Yvonne S. DavidsonSamantha RabyDavid M. A. Mann Original Paper 04 October 2011 Pages: 703 - 713
Acute and chronically increased immunoreactivity to phosphorylation-independent but not pathological TDP-43 after a single traumatic brain injury in humans Victoria E. JohnsonWilliam StewartDouglas H. Smith Original Paper 19 November 2011 Pages: 715 - 726
A proteomic study identifies different levels of light chain ferritin in corticobasal degeneration and progressive supranuclear palsy Abdul Shukkur EbrahimJayanarayan KulathingalDaniel Sevlever Original Paper 20 October 2011 Pages: 727 - 736
Simulated brain biopsy for diagnosing neurodegeneration using autopsy-confirmed cases Sriram VennetiJohn L. RobinsonJohn Q. Trojanowski Original Paper 30 September 2011 Pages: 737 - 745
Fas/FasL-mediated apoptosis and inflammation are key features of acute human spinal cord injury: implications for translational, clinical application Wen Ru YuMichael G. Fehlings Original Paper Open access 29 October 2011 Pages: 747 - 761
Inner ear lesions in congenital cytomegalovirus infection of human fetuses Natacha TeissierAnne-Lise DelezoideHoma Adle-Biassette Original Paper 28 October 2011 Pages: 763 - 774
An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene Satoshi O. SuzukiToru IwakiAkiko Iwaki Case Report 20 November 2011 Pages: 775 - 781
Multinodular leptomeningeal metastases from ETANTR contain both small blue cell and maturing neuropil elements B. K. Kleinschmidt-DeMastersArianne BoylanNicholas K. Foreman Correspondence 28 October 2011 Pages: 783 - 785
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with loss of morphological but retained genetic key features during progression Adelheid WoehrerIrene SlavcChristine Haberler Correspondence 06 November 2011 Pages: 787 - 790
Activating L265P mutations of the MYD88 gene are common in primary central nervous system lymphoma Manuel Montesinos-RongenElzbieta GodlewskaMartina Deckert Correspondence 22 October 2011 Pages: 791 - 792