1. Protein degradation pathways in Parkinson’s disease: curse or blessing

   • Darius Ebrahimi-Fakhari
   • Lara Wahlster
   • Pamela J. McLean

   Review 29 June 2012 Pages: 153 - 172

   

2. Autophagic adapter protein NBR1 is localized in Lewy bodies and glial cytoplasmic inclusions and is involved in aggregate formation in α-synucleinopathy

   • Saori Odagiri
   • Kunikazu Tanji
   • Koichi Wakabayashi

   Original Paper 07 April 2012 Pages: 173 - 186

   

3. Long-term proteasomal inhibition in transgenic mice by UBB⁺¹ expression results in dysfunction of central respiration control reminiscent of brainstem neuropathology in Alzheimer patients

   • Martin Irmler
   • Romina J. G. Gentier
   • Johannes Beckers

   Original Paper Open access 23 June 2012 Pages: 187 - 197

   

4. Mitochondrial DNA polymorphisms specifically modify cerebral β-amyloid proteostasis

   • Katja Scheffler
   • Markus Krohn
   • Jens Pahnke

   Original Paper 18 April 2012 Pages: 199 - 208

   

5. Clonally expanded mitochondrial DNA deletions within the choroid plexus in multiple sclerosis

   • Graham R. Campbell
   • Yevgenya Kraytsberg
   • Don J. Mahad

   Original Paper 12 June 2012 Pages: 209 - 220

   

6. Distinct TDP-43 pathology in ALS patients with ataxin 2 intermediate-length polyQ expansions

   • Michael P. Hart
   • Johannes Brettschneider
   • Aaron D. Gitler

   Original Paper 21 April 2012 Pages: 221 - 230

   

7. TDP-43 regulates the mammalian spinogenesis through translational repression of Rac1

   • Pritha Majumder
   • Yi-Ting Chen
   • Che-Kun James Shen

   Original Paper 04 July 2012 Pages: 231 - 245

   

8. Distinct disease-risk groups in pediatric supratentorial and posterior fossa ependymomas

   • Catherine Godfraind
   • Joanna M. Kaczmarska
   • David W. Ellison

   Original Paper 21 April 2012 Pages: 247 - 257

   

9. Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma

   • Cynthia L. Andoniadou
   • Carles Gaston-Massuet
   • Juan Pedro Martinez-Barbera

   Original Paper Open access 18 February 2012 Pages: 259 - 271

   

10. Next generation sequencing for molecular diagnosis of neuromuscular diseases

    • Nasim Vasli
    • Johann Böhm
    • Jocelyn Laporte

    Original Paper Open access 18 April 2012 Pages: 273 - 283

    

11. TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation

    • Maria Martinez-Lage
    • Laura Molina-Porcel
    • John Q. Trojanowski

    Case Reports 03 February 2012 Pages: 285 - 291

    

12. Periventricular white matter immunoglobulin lambda light chain deposition disease diagnosed by proteomic analysis

    • Joshua R. Menke
    • Mark E. Jentoft
    • Caterina Giannini

    Correspondence 04 July 2012 Pages: 293 - 295