1. Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri

   • Pepijn van den Munckhof
   • Imke Christiaans
   • Theo J. M. Hulsebos

   ORIGINAL ARTICLE 26 October 2011 Pages: 1 - 7

   

2. Restriction of trophic factors and nutrients induces PARKIN expression

   • M. Klinkenberg
   • S. Gispert
   • M. Jendrach

   ORIGINAL ARTICLE Open access 26 October 2011 Pages: 9 - 21

   

3. Distinct DNA binding and transcriptional repression characteristics related to different ARX mutations

   • Ginam Cho
   • MacLean P. Nasrallah
   • Jeffrey A. Golden

   Original Article 18 January 2012 Pages: 23 - 29

   

4. Genotype–phenotype correlation in interstitial 6q deletions: a report of 12 new cases

   • Jill A. Rosenfeld
   • Dina Amrom
   • Lisa G. Shaffer

   Original Article 05 January 2012 Pages: 31 - 47

   

5. Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalus

   • Mariola Marx
   • Simone Diestel
   • Michael K. E. Schäfer

   Original Article 06 January 2012 Pages: 49 - 59

   

6. New brain-specific beta-synuclein isoforms show expression ratio changes in Lewy body diseases

   • Katrin Beyer
   • Ana M. Munoz-Marmol
   • Aurelio Ariza

   Original Article 29 December 2011 Pages: 61 - 72

   

7. Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)

   • Peter Bauer
   • Esther Leshinsky-Silver
   • Ludger Schöls

   Original Article 31 January 2012 Pages: 73 - 76

   

8. Vincristine exacerbates asymptomatic Charcot–Marie–Tooth disease with a novel EGR2 mutation

   • Tomonori Nakamura
   • Akihiro Hashiguchi
   • Hiroshi Takashima

   Original Article 25 January 2012 Pages: 77 - 82

   

9. Independent replication of STAT3 association with multiple sclerosis risk in a large German case–control sample

   • Christina M. Lill
   • Brit-Maren M. Schjeide
   • Frauke Zipp

   Short Communication 18 November 2011 Pages: 83 - 86

10. Genome-scale methylation analysis of Parkinson's disease patients' brains reveals DNA hypomethylation and increased mRNA expression of cytochrome P450 2E1

    • Oliver Kaut
    • Ina Schmitt
    • Ullrich Wüllner

    Short Communication 12 January 2012 Pages: 87 - 91

    

11. Neuroferritinopathy: a new inborn error of iron metabolism

    • Michael J. Keogh
    • Patricia Jonas
    • John Burn

    Short Communication 26 January 2012 Pages: 93 - 96

    

12. Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort

    • B. H. Maher
    • M. Kerr
    • L. R. Griffiths

    Short Communication 01 February 2012 Pages: 97 - 101

13. Comment on the article “Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri” by van den Munckhof et al.

    • Trine E. Prescott
    • Miriam J. Smith
    • D. Gareth Evans

    Letter to the Editors 28 December 2011 Pages: 103 - 104