Analyzing dendritic spine pathology in Alzheimer’s disease: problems and opportunities Mario M. DorostkarChengyu ZouJochen Herms Review Open access 11 June 2015 Pages: 1 - 19
Beta-amyloid deposition in chronic traumatic encephalopathy Thor D. SteinPhilip H. MontenigroAnn C. McKee Original Paper 06 May 2015 Pages: 21 - 34
Aβ43 is neurotoxic and primes aggregation of Aβ40 in vivo Sylvie BurnoufMarianna Karina GorskyLinda Partridge Original Paper Open access 11 April 2015 Pages: 35 - 47
Low molecular weight species of TDP-43 generated by abnormal splicing form inclusions in amyotrophic lateral sclerosis and result in motor neuron death Shangxi XiaoTeresa SanelliJanice Robertson Original Paper Open access 19 March 2015 Pages: 49 - 61
Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy Johnathan Cooper-KnockAdrian HigginbottomPamela J. Shaw Original Paper Open access 06 May 2015 Pages: 63 - 75
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease Cyril PottierKevin F. BieniekRosa Rademakers Original Paper 06 May 2015 Pages: 77 - 92
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein Naoya AokiPhilip J. BoyerDennis W. Dickson Original Paper 12 May 2015 Pages: 93 - 105
Induction of endogenous Type I interferon within the central nervous system plays a protective role in experimental autoimmune encephalomyelitis Reza KhorooshiMarlene Thorsen MørchTrevor Owens Original Paper Open access 14 April 2015 Pages: 107 - 118
Alterations of mGluR5 and its endogenous regulators Norbin, Tamalin and Preso1 in schizophrenia: towards a model of mGluR5 dysregulation Natalie MatosinFrancesca Fernandez-EnrightKelly Anne Newell Original Paper 17 March 2015 Pages: 119 - 129
Identification of a novel MET mutation in high-grade glioma resulting in an auto-active intracellular protein Anna C. NavisSanne A. M. van LithWilliam P. J. Leenders Original Paper Open access 11 April 2015 Pages: 131 - 144
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration Masataka NakamuraKevin F. BieniekKevin B. Boylan Case Report 28 April 2015 Pages: 145 - 157